US20100310554A1 - Methods for Reversing Multiple Resistance in Animal Cells - Google Patents

Methods for Reversing Multiple Resistance in Animal Cells Download PDF

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US20100310554A1
US20100310554A1 US12/556,560 US55656009A US2010310554A1 US 20100310554 A1 US20100310554 A1 US 20100310554A1 US 55656009 A US55656009 A US 55656009A US 2010310554 A1 US2010310554 A1 US 2010310554A1
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protein
promoter
present
adenovirus
cells
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Per Sonne Holm
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Priority to US12/556,560 priority Critical patent/US20100310554A1/en
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Priority to US13/170,395 priority patent/US20110286999A1/en
Priority to US15/461,668 priority patent/US11369650B2/en
Priority to US17/752,436 priority patent/US20220339219A1/en
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/76—Viruses; Subviral particles; Bacteriophages
    • A61K35/761—Adenovirus
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • C12N15/86—Viral vectors
    • C12N15/861—Adenoviral vectors
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N7/00—Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
    • C12N2710/00011—Details
    • C12N2710/10011—Adenoviridae
    • C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
    • C12N2710/10321—Viruses as such, e.g. new isolates, mutants or their genomic sequences
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
    • C12N2710/00011—Details
    • C12N2710/10011—Adenoviridae
    • C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
    • C12N2710/10332—Use of virus as therapeutic agent, other than vaccine, e.g. as cytolytic agent

Definitions

  • the invention is related to means for reversing multiple drug resistance in animal cells.
  • tumour cells are more prone to chemosensitivity due to their increased proliferation rate.
  • Good therapeutic results can be obtained for various tumour entities such as juvenile lymphatic leukaemia, some lymphoma and testicular carcinoma. However, these tumours represent only 10% of all malignant diseases. Most of the solid tumours do not respond or respond only weakly to a treatment using various cytostatics.
  • carcinoma derived from kidney, colon, pancreas and liver as well as melanoma and brain tumours.
  • mammary carcinoma, ovarian carcinoma and prostate carcinoma initially respond well to cytostatic treatment, however, get insensitive to the cytostatics used in the course of the therapeutical cycles.
  • studies show that there is a high correlation between P-glycoprotein expression and occurrence of metastases.
  • tumour cell heterogeneity and vascularization of the tumour genetic and epigenetic changes of the tumour cells themselves are involved in the formation of resistance to cytostatics and radiation.
  • cytostatics and radiation These can be grouped into the following six major groups: 1. increased efflux activity; 2. modulation of the target protein; 3. increased repair; 4. modulation of apoptosis; 5. cell cycle; and 6. decreased influx.
  • MDR multidrug resistance
  • the MDR1 protein which is also referred to as Pgp and P-glycoprotein, respectively, is part of the group of ABC transporters to which, among others, also the MRP (multidrug related protein) and BCRP (breast cancer resistance protein) belong.
  • the vesicular LRP protein lung resistance-related protein
  • the vesicular LRP protein does not belong to the classical ABC transporter. However, it is also mentioned quite frequently in this connection, as it is also involved in transport processes related to the formation of resistance to cytostatics in tumour cells (Sugawara I et al., CANCER LETTERS 112, 23-31, 1997; Gottesman et al., Nat Rev Cancer. 2002, 2:48-58).
  • the LRP promoter comprises an inverted CAAT-box (Y-box) (Scheider et al., Breast Cancer Res., 2001, 3, 183-191).
  • the problem underlying the present invention is to provide means for the treatment of such diseases, in particular for the treatment of the afore-described resistant diseases, i.e. tumors and tumor diseases the cells of which are resistant to cytostatics and/or radiation.
  • the problem underlying the present invention is to reverse or eliminate the afore-described and other resistances described herein.
  • the problem underlying the present invention is to provide means for restoring drug sensitivity, in particular drug sensitivity of cells forming or involved in tumour and tumour diseases, whereby such cells are not sensitive or no longer sensitive to cytostatics and/or radiation.
  • viruses in particular adenoviruses, which replicate in a YB-1 dependent mariner.
  • these problems are solved in accordance with the present invention by the subject matter of the attached independent claims. Preferred embodiments result from the attached dependent claims.
  • the problem underlying the present invention is thus also solved in a first aspect by the use of a virus, preferably an adenovirus for reversing resistance in cells.
  • the problem underlying the present invention is thus also solved in a second aspect by the use of a virus, preferably an adenovirus for the manufacture of a medicament for reversing resistances in cells.
  • a virus preferably an adenovirus for the manufacture of a medicament for reversing resistances in cells.
  • the problem underlying the present invention is thus also solved in a third aspect by the use of a virus, preferably an adenovirus for restoring drug sensitivity of cells.
  • the problem underlying the present invention is thus also solved in a fourth aspect by the use of a virus, preferably an adenovirus for the manufacture of a medicament for restoring drug sensitivity of cells.
  • cells are animal cells, preferably mammalian cells and more preferably human cells.
  • the cells are tumor cells.
  • the cells have a resistance to or are insensitive to one or several pharmaceutically active agents and/or radiation.
  • the pharmaceutically active agent is a cytostatic.
  • the problem underlying the present invention is thus also solved in a fifth aspect by the use of a virus, preferably an adenovirus for inhibiting ABC transporters, in particular the expression of ABC transporters.
  • the resistance is mediated by an ABC transporter.
  • the resistance is a multiple resistance or polyresistance, particular a multiple or polyresistance against cytostatics and/or radiation.
  • a virus preferably an adenovirus for the manufacture of a medicament for the treatment of diseases, in particular tumor diseases, whereby the cells involved in the disease or a part thereof, are resistant, in particular have an ABC transporter mediated resistance and/or a multiple resistance or polyresistance, preferably a multiple resistance or polyresistance against cytostatics and/or radiation.
  • the treatment comprises the administration of the adenovirus and a further pharmaceutically active agent, or the administration of an adenovirus and radiation of the cell or the organism to be treated, whereby the administration of the adenovirus causes or increases the efficacy of the further pharmaceutically active agent and/or of the radiation.
  • the treatment comprises the administration of the adenovirus and a further pharmaceutically active agent or the administration of an adenovirus and radiation of the cell or the organism to be treated, whereby the administration of the further pharmaceutically active agent and/or the radiation causes or increases the efficacy of the adenovirus.
  • the ABC transporter is selected from the group comprising MRP and MDR, in particular MDR-1.
  • the adenovirus is administered at least at the beginning of the treatment prior to the administration of the further pharmaceutically active agent.
  • the adenovirus is administered at least prior to the radiation at the beginning of the treatment.
  • the adenovirus is administered about 1 to 3 days, preferably about 1 to 2 days prior to the administration of the further pharmaceutically active agent or prior to the radiation.
  • the resistance is a resistance against cytostatics and/or radiation.
  • the further pharmaceutically active agent is selected from the group comprising cytostatics.
  • the radiation is a radiation as used in the radiation of tumor diseases.
  • the radiation is performed at a dosage and using a radiation regimen and/or that the further pharmaceutically active agent is administered at a dosage or in accordance with a treatment regimen as with patients, whereby the patients are selected from the group comprising immune suppressed patients, patients having a bad or pathological blood picture and patients having bad or pathological kidney values.
  • the radiation is performed at the dosage or in accordance with a radiation regimen and/or the further pharmaceutically active agent is administered at a dosage or in accordance with a treatment regimen as in connection with patients suffering from a disease, whereby the cells involved in such disease or a part thereof are not resistant.
  • the administration of the adenovirus creates the prerequisite for the administration of the further pharmaceutically active agent or for the radiation.
  • the adenovirus is present as a virus, nucleic acid, vector, replication system, medicament or pharmaceutically composition.
  • the adenovirus is replicating in a YB-1 dependent manner.
  • the adenovirus is E1A minus.
  • the adenovirus is an oncolytic adenovirus.
  • the virus preferably an adenovirus
  • the virus is replication deficient in cells which lack YB-1 in the nucleus, and whereby the virus encodes an oncogene or oncogene product, in particular an oncogene protein, which transactivates at least one viral gene, preferably an adenoviral gene, whereby the gene is selected from the group comprising E1B55kDa, E4orf6, E4orf3 and E3ADP.
  • the virus in particular the adenovirus replicates in cells which have YB-1 in the nucleus.
  • the viral oncogene protein is E1A and/or the oncogene is the gene coding for E1A and/or the oncogene protein E1A.
  • the viral oncogene protein E1A is capable of binding a functional Rb tumor suppressor gene product.
  • the viral oncogene protein E1A is incapable of binding a functional Rb tumor suppressor gene product.
  • the viral oncoprotein E1A does not induce the localisation of YB-1 into the nucleus.
  • the medicament is for patients whose cells are Rb positive or Rb negative.
  • the cells are Rb negative and the cell nucleus is YB-1 positive, preferably YB-1 positive in the nucleus independent from the cell cycle.
  • the cells are p53 positive or p53 negative.
  • the oncogene protein exhibits one or several mutations or deletions compared to the wildtype oncogene protein E1A, whereby the deletion is preferably one selected from the group comprising deletions of the CR3 stretches and deletions of the N-terminus and deletions of the C-terminus.
  • the E1A oncogene protein is capable of binding to Rb.
  • the oncogene protein comprises one or several mutations or deletions compared to the wildtype oncogene protein, whereby the deletion is preferably a deletion in the CR1 region and/or CR2 region.
  • the oncogene protein E1A is incapable of binding to Rb.
  • the viral oncogene protein preferably E1A
  • the virus particularly the adenovirus, codes for YB-1.
  • first, second, third, fourth, fifth and sixth aspect YB-1 is under the control of a tissue-specific and/or tumor-specific promoter.
  • the virus preferably the adenovirus, codes for at least one protein, whereby the protein is selected from the group comprising E4orf6, E4orf3, E1B55k and adenoviral E3ADP protein.
  • the cells comprise YB-1 in the nucleus, preferably that the cells forming the tumor or part thereof have YB-1 in the nucleus.
  • the tumor comprises YB-1 in the nucleus after induction of the transport of YB-1 into the nucleus.
  • the transport of YB-1 into the nucleus is triggered by at least one measure selected from the group comprising irradiation, administration of cytostatics and hyperthermia.
  • the measure is applied to a cell, an organ or an organism, preferably an organism in need thereof, more preferably an organism suffering from said disease.
  • the virus preferably the adenovirus
  • the adenovirus is selected from the group comprising Ad ⁇ 24, dl922-947, E1 Ad/01/07, dl1119/1131, CB 016, dl520 and viruses lacking an expressed viral oncogene which is capable of binding a functional Rb tumor suppressor gene product.
  • the virus preferably the adenovirus
  • the replication is controlled by YB-1 through the activation of the E2-late promoter, preferably the activation is predominantly controlled through the activation of the E2-late promoter.
  • the virus comprises a nucleic acid coding for a transgene.
  • the virus comprises the translation and/or transcription product of a transgene.
  • the nucleic acid comprises a transgene or a nucleic acid coding for a transgene.
  • the transgene is selected from the group comprising prodrug genes, cytokines and genes for cytokines, apoptosis-inducing genes, tumor suppressor genes, genes for metalloproteinase inhibitors and genes for angiogenesis inhibitors.
  • the transgene is selected from the group comprising nucleic acids for siRNA, for aptamers, for antisense molecules and for ribozymes, whereby the siRNA, the aptamer, the antisense molecule and/or the ribozyme are targeting a target molecule.
  • the target molecule is selected from the group comprising resistance relevant factors, anti-apoptosis factors, oncogenes, angiogenesis factors, DNA synthesis enzymes, DNA repair enzymes, growth factors, receptors for growth factors, transcription factors, metalloproteinases, preferably matrix metalloproteinase kinases, and plasminogen activator of the urokinase type.
  • the medicament further comprises at least one pharmaceutically active agent.
  • the pharmaceutically active agent is selected from the group comprising cytokines, metalloproteinase inhibitors, angiogenesis inhibitors, cytostatics, cell cycle inhibitors, proteosome inhibitors, recombinant antibodies, inhibitors of the signal transduction pathway and inhibitors of protein kinases.
  • the medicament comprises a combination of at least two agents, whereby each of said agents is individually and independently selected from the group comprising cytostatics.
  • At least two of the agents are targeting different target molecules.
  • At least two of the agents are active through different modes of action.
  • At least one agent increases the infectability of the cell in which the virus replicates.
  • At least one agent affects the availability of a component of the cell, preferably increases the availability of the component, whereby the component mediates the uptake of the virus.
  • At least one agent mediates the transport of YB-1 into the nucleus, preferably increases the same.
  • At least one agents is a histone deacetylase inhibitor.
  • the histone deacetylase inhibitor is selected from the group comprising trichostatine A, FR901228, MS-27-275, NVP-LAQ824, PXD101, apicidine and striptaid.
  • the at least one agent is selected from the group comprising trichostatine A, FR901228, MS-27-275, NVP-LAQ824, PXD101, apicidine and striptaid.
  • At least one agent is a topoisomerase inhibitor.
  • the topoisomerase inhibitor is selected from the group comprising Camptothecin, Irinotecan, Topotecan, DX-895If, SN-38, 9-aminocamptothecin, 9-nitrocamptothecin, Daunorubicn and Etoposid.
  • the medicament comprises trichostatin A and irinotecan.
  • the virus in particular the virus as described in connection with any of the first, second, third, fourth, fifth and sixth aspect, is separated from the at least two agents in said medicament.
  • At least one unit dosage of the virus is separated from at least one unit dose of one or the at least two agents.
  • the virus preferably expresses a first protein which is selected from the group comprising an E1B protein and an E4 protein, prior to a second protein which is selected from the group comprising an E1A-protein.
  • the first protein is an E1B protein, preferably an E1B55kd protein.
  • the first protein is an E4 protein, preferably an E4orf6 protein.
  • the first protein is a combination of E1B protein and E4 protein, preferably a combination of E1B55kD protein and E4orf6 protein.
  • the E1A protein is an E1A12S protein.
  • the virus comprises at least one nucleic acid coding for a protein which is selected from the group comprising E1B proteins, E4 proteins and E1A proteins, whereby the at least one protein is under the control of a promoter which is different from the promoter controlling the expression of the protein in a wildtype adenovirus.
  • the at least one protein is an E1B protein, preferably an E1B55kD protein.
  • the at least one protein is an E4 protein, preferably an E4orf6 protein.
  • At least one protein is an E1A protein, preferably an E1A12S protein.
  • the at least one protein is a combination of E1B protein and E4 protein, preferably a combination of E1B55kD protein and E4orf6 protein.
  • the at least one protein is a combination of E1B protein and E1A protein, preferably a combination of E1B55kD protein and E1A12S protein.
  • the at least one protein is a combination of E4 protein and E1A protein, preferably a combination of E4orf6 protein and E1A12S protein.
  • the at least one protein is a combination of E1B protein, E4 protein and E1A protein, preferably a combination of E1B55kD protein, E4orf6 protein and E1A12S protein.
  • the expression of the E1B protein is controlled by a promoter, whereby the promoter is selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters, whereby the adenoviral promoter is different from the E1B promoter.
  • the expression of the E4 protein is controlled by a promoter, whereby the promoter is selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters, whereby the adenoviral promoter is different from the E4 promoter.
  • the adenoviral promoter is the E1A promoter.
  • the expression of the E1A protein is controlled by a promoter, whereby the promoter is selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters, whereby the adenoviral promoter is different from the E1A promoter.
  • the expression of the E1A protein is YB-1 controlled or can be regulated by YB-1.
  • the promoter controlling the expression of the E1A protein is the adenoviral E2 late promoter.
  • the E4 protein, preferably the E4orf6 protein, and the E1B protein, preferably the E1B55kd protein are under the control of the same or a common promoter.
  • the virus provides YB-1 in the nucleus through at least one adenoviral protein or mediates the provision of YB-1 in the nucleus through at least one adenoviral protein, whereby preferably the adenoviral protein is different from E1A.
  • the virus provides YB-1 for adenoviral replication through at least one adenoviral protein or mediates the provision of YB-1 for adenoviral replication through at least one adenoviral protein, whereby preferably the adenoviral protein is different from E1A.
  • the adenoviral protein is a complex of E4orf6 and E1B55kd.
  • the nucleic acid of the adenovirus comprises at least one functionally inactive adenoviral region, whereby the region is selected from the group comprising the E1 region, the E3 region, the E4 region and combinations thereof.
  • the region is the E1 region.
  • the region is the E3 region.
  • the region is the E4 region.
  • the region comprises the E1 region, the E3 region and the E4 region.
  • the virus comprises at least one expression cassette, whereby the expression cassette comprises at least one promoter and a nucleic acid coding for an adenoviral protein, whereby the adenoviral protein is an E1B protein, preferably an E1B55kD protein.
  • the promoter is different from the E1B promoter.
  • the promoter is selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters, whereby the promoter is different from the E1B promoter.
  • the virus comprises at least one expression cassette, whereby the expression cassette comprises at least one promoter and a nucleic acid coding for an adenoviral protein, whereby the adenoviral protein is an E4 protein, preferably an E4orf6 protein.
  • the promoter is different from the E4 promoter.
  • the promoter is selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters, whereby the adenoviral promoter is different from the E4 promoter.
  • the promoter is the E1A promoter.
  • the virus comprises at least one expression cassette, whereby the expression cassette comprises at least one promoter and a nucleic acid coding for an adenoviral protein, whereby the adenoviral protein is an E1A protein, preferably an E1A12S protein.
  • the promoter is different from the E1A promoter.
  • the promoter is selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters.
  • the adenovirus comprises a nucleic acid, whereby the nucleic acid codes for YB-1.
  • nucleic acid coding for YB-1 is under the control of a promoter, whereby the promoter is preferably the E2 late promoter.
  • nucleic acid coding for YB-1 is under the control of a promoter, whereby the promoter is YB-1 dependent and YB-1 controlled, respectively.
  • nucleic acid coding for YB-1 is part of the expression cassette comprising a nucleic acid coding for an E1A protein, preferably a nucleic acid coding for an E1A12S protein.
  • nucleic acid coding for the E1A protein is separated from the nucleic acid coding for YB-1 through an IRES sequence.
  • nucleic acid coding for the E4 protein preferably the E4orf6 protein
  • nucleic acid coding for the E1B protein preferably the E1B55kD protein
  • an expression cassette whereby preferably the two coding sequences are separated through an IRES sequence.
  • the promoter of the expression cassette is selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters, whereby the adenoviral promoter is different from the E4 promoter and different from the E1B promoter, preferably different from the wildtype E4 promoter and different from the wildtype E1B promoter.
  • the virus comprises an expression cassette comprising a promoter and a nucleic acid sequence, whereby the nucleic acid sequence is selected from the group comprising aptamers, ribozymes, aptazymes, antisense molecules and siRNA.
  • the virus comprises an expression cassette comprising a promoter and a nucleic acid sequence, whereby the nucleic acid sequence is a coding nucleic acid, whereby the nucleic acid codes for a molecule which is selected from the group comprising peptides, polypeptides, proteins, anticalines, antibodies and antibody fragments.
  • the virus comprises an expression cassette, whereby the expression cassette comprises a promoter and a nucleic acid sequence, whereby the nucleic acid sequence is selected from the group comprising apoptosis inducing genes, prodrug genes, protease inhibitors, tumor suppressor genes, cytokines and angiogenesis inhibitors.
  • the virus is a recombinant adenovirus.
  • the virus is an adenovirus mutant.
  • the virus is replication deficient.
  • the virus is capable of replicating in cells comprising deregulated YB-1 or having YB-1 in the nucleus.
  • the cells contain YB-1 in the nucleus independent of the cell cycle.
  • the medicament comprises at least one further pharmaceutically active agent.
  • the medicament is administered together with a further pharmaceutically active agent or is intended therefor.
  • the further pharmaceutically active agent is selected from the group comprising cytokines, metalloproteinase inhibitors, angiogenesis inhibitors, cytostatics, tyrosine kinase inhibitors, cell cycle inhibitors, proteosome inhibitors, inhibitors of the signal transduction cascade, inhibitors of protein kinase and recombinant antibodies.
  • the medicament comprises a combination of at least two agents, whereby each agent is individually and independently selected from the group comprising cytostatics.
  • At least two of the agents are targeting different target molecules.
  • At least two of the agents are active through different modes of action.
  • At least one agent increases the infectability of a cell in which the virus replicates.
  • the agent affects the availability of a component of the cell, preferably increases the availability of the component, whereby the component mediates the uptake of the virus.
  • the agent mediates the transport of YB-1 into the nucleus, preferably increases the transport YB-1 into the nucleus.
  • the agent is a histone deacetylase inhibitor.
  • the histone deacetylase inhibitor is selected from the group comprising trichostatine A, FR901228, MS-27-275, NVP-LAQ824, PXD101, apicidine and striptaid.
  • At least one agent is selected from the group comprising trichostatine A, FR901228, MS-27-275, NVP-LAQ824, PXD101, apicidine and striptaid.
  • At least one agent is a topoisomerase inhibitor.
  • the topoisomerase inhibitor is selected from the group comprising Camptothecin, SN-38, Topotecan, DX-895If, Irinotecan, 9-aminocamptothecin, 9-nitrocamptothecin, Etoposid and Daunorubicin.
  • the agent comprises trichostatine A and irinotecan.
  • the virus comprises:
  • the virus expresses a nucleic acid coding for protein IX and expresses protein IX.
  • the lacking functional wildtype E1A region is E1A-minus.
  • the lacking functional wildtype E1 region is E1B-minus.
  • the lacking wildtype E1 region is E 1B55k-minus and/or E1B19k-minus and/or protein IX-minus.
  • the transporter is a transporter as provided by the virus preferably a heterologous transporter.
  • the transporter is a viral transporter.
  • the transporter comprises the protein E4orf6.
  • the transporter comprises the protein E1B55k.
  • the transporter comprises a complex consisting of E4orf4 and E1B55k.
  • the transporter is encoded by a nucleic acid, whereby the nucleic acid is under the control of a promoter.
  • the transporter is a complex consisting of at least two factors, whereby each factor is encoded by a nucleic acid, whereby both nucleic acids are controlled by a common promoter.
  • the two coding nucleic acids are linked through an element regulating the expression level and whereby the element is preferably selected from the group comprising IRES.
  • the transporter is a complex consisting of at least two factors and each factor is encoded by a nucleic acid, whereby both nucleic acids are each controlled by an own promoter.
  • the promoter is different from the E4 promoter, in particular from the adenoviral E4 promoter, and is different from the E1B promoter, in particular from the adenoviral E1B promoter.
  • the promoter is selected from the group comprising tissue-specific promoters, tumor-specific tumors, viral promoters, CMV-promoters, in particular adenoviral promoters, under the proviso that they are different from the E4 promoter, the E1B promoter and preferably also different from the E2-late promoter.
  • the nucleic acid coding for the transporter comprises a 3′-UTR of the E1B55k at the 3′ of the E1B55k.
  • the nucleic acid coding for the transporter does not comprise a nucleic acid coding for E1B55k.
  • nucleic acid coding for the transporter codes for E1B55k and E1B19k.
  • nucleic acid coding for the transporter also codes for protein IX.
  • nucleic acid coding for E1B55k and E1B19k is under the control of a promoter.
  • nucleic acid coding for E1B55k and/or E1B19k and/or protein IX is under the control of a promoter, whereby the promoter is preferably different from an E1A-dependent promoter, whereby more preferably the nucleic acid codes for E1B55k, E1B19k and protein IX.
  • the lacking functional wildtype E1 region is E1A13S-minus and/or E1A12S-minus.
  • the lacking functional wildtype E1 region is E1A13S-minus.
  • the lacking wildtype E1 region is E1A13S-minus and E1A12-minus, whereby the virus comprises a nucleic acid coding for the E1A12S protein, whereby the nucleic acid is preferably a heterologous nucleic acid.
  • the nucleic acid coding for the E1A12S protein is under the control of a promoter, whereby the promoter is preferably a YB-1-dependent promoter and is more preferably selected from the group comprising the E2-late promoter, tumor-specific promoters and tissue-specific promoters.
  • the promoter is preferably a YB-1-dependent promoter and is more preferably selected from the group comprising the E2-late promoter, tumor-specific promoters and tissue-specific promoters.
  • nucleic acid(s) coding for the transporter codes/code for E4orf6 and E1B55k.
  • nucleic acid coding for E1A12S and the nucleic acid coding for the protein IX are under the control of a common promoter, whereby preferably both coding nucleic acids are linked to each other through an element regulating the expression, whereby the element is more preferably selected from the group comprising IRES.
  • nucleic acid coding for the E1A12S region and the nucleic acid coding for the protein IX are each under the control of a promoter, whereby the promoter preferably is the same promoter.
  • the promoter is a YB-1-dependent promoter, which is preferably selected from the group comprising the E2-late promoter, the MDR promoter and the DNA polymerase alpha promoter.
  • the virus comprises a nucleic acid coding for YB-1.
  • nucleic acid coding for the E1A12S protein and the nucleic acid coding for the YB-1 are under the control of a common promoter, whereby both coding nucleic acids are linked to each other by an expression-regulating element, whereby the element is preferably selected from the group comprising IRES.
  • nucleic acid coding for YB-1 and the nucleic acid coding for the E1A12S protein are each under the control of a promoter, whereby the promoter is preferably the same promoter.
  • the promoter is a YB-1-dependent promoter which is preferably selected from the group comprising the E2-late promoter, the MDR promoter and the DNA polymerase alpha promoter.
  • nucleic acid coding for the E1A12S is cloned into the E3 region or the E4 region.
  • nucleic acid coding for the E1A12S and the nucleic acid coding for protein IX or the nucleic acid coding for YB-1 are cloned into the E3 region or the E4 region.
  • the expression of the nucleic acid coding for the protein IX is controlled by a promoter different from E1B, by E1B19k or by E1A12S.
  • the virus comprises at least a transgene which is preferably cloned in to the E3 region.
  • the virus comprises at least a transgene which is preferably cloned into the E4 region.
  • virus comprises:
  • virus comprises:
  • the virus is replication deficient in cells which do not contain YB-1 in the nucleus.
  • the virus is capable of replicating in cells which have YB-1 in the nucleus, in particular have YB-1 in the nucleus independent of the cell cycle.
  • the virus is capable of replicating in cells in which YB-1 is present in a deregulated manner.
  • the medicament further comprises at least a pharmaceutically active agent.
  • the pharmaceutically active agent is selected from the group comprising cytokines, metalloproteinases inhibitors, angiogenesis inhibitors, cytostatics, cell cycle inhibitors, proteosome inhibitors, recombinant antibodies, inhibitors to the signal transduction cascade and protein kinases.
  • the medicament comprises a combination of at least two agents, whereby each agent is individually and independently selected from the group comprising cytostatics.
  • At least two of the agents are targeting different target molecules.
  • At least two of the agents are active through a different mode of action.
  • At least one agent increases the infectability of a cell in which the virus replicates.
  • At least one agent affects the availability of a compound in the cell, preferably increases the availability of the compound, whereby the compound mediates the uptake of the virus.
  • the agent mediates the transport of YB-1 to the nucleus, preferably increases the transport of YB-1 into the nucleus.
  • At least one agent is a histone deacetylase inhibitor.
  • the histone deacetylase inhibitor is selected from the group comprising Trichostatin A, FR 901228, MS-27-275, NVP-LAQ824, PXD101 Apicidin and Scriptaid.
  • the agent is selected from the group comprising Trichostatin A, FR 901228, MS-27-275, NVP-LAQ824, PXD101 Apicidin and Scriptaid.
  • At least one agent is a topoisomerase inhibitor.
  • the topoisomerase inhibitor is selected from the group comprising Camptothecin, Irinotecan, Topotecan, DX-895If, SN-38, 9-aminocamptothecin, 9-nitrocamptothecin, Daunorubicn and Etoposid.
  • the agent comprises trichostatine A and irinotecan.
  • the virus in particular a virus according to any of the preceding claims, is separated from the at least two agents.
  • At least one unit dosage of the virus is separated from at least one unit dosage of one of or of the at least two agents.
  • a seventh aspect the problem underlying the present invention is solved by a medicament as defined with the use of the viruses in connection with the present invention.
  • the problem underlying the present invention is solved by a method for the treatment of a patient in need thereof, whereby the medicament as defined and discloses, respectively, herein is administered to said patient.
  • adenovirus which require YB-1 for replication i.e. which are replicating in a YB-1 dependent manner, are suitable to eliminate and reverse, respectively, resistance of cells, in particular of animal cells.
  • YB-1 due to the use of YB-1 in the replication of the YB-1 dependent viruses, YB-1 is no longer available as an important factor for the formation of resistances.
  • YB-1 due to its involvement in the replication of this group of viruses and adenoviruses in particular, seems to be removed to such extent or no longer available to such extent that other YB-1 controlled processes, such as the YB-1 controlled transcription of resistance mediating genes, are no longer proceeding or, at least, are proceeding in a significantly reduced manner.
  • any virus can be used in connection with the present invention and for the uses described herein, whereby such virus uses YB-1 for its replication, whereby preferably the replication results in the lyses of the infected cells (also referred to as CPE; cytopathic effect) and not only in transient replication.
  • the kind of resistance which is reduced or reversed is basically only limited to those resistances, the transcription, translation and/or activity of which is controlled by YB-1, preferably activated by YB-1.
  • Y-box inverted CAAT-box
  • Such resistances are in particular the following ones.
  • Classical and atypic multidrug resistance (MDR) whereby apart from the atypical multidrug resistance the classical phenotype of MDR is based on the overexpression of a membrane-bound 170 kDa ATP-dependent, transmembrane glycoprotein which predominantly exports lipophilic compounds from the cell.
  • the MDR1-protein or also Pgp and P-glycoprotein, respectively, are members of the group of ABC transporters to which, among others, also MRP (multidrug related protein) and BCRP (breast cancer resistance protein) belong. Accordingly, further resistances in the meaning of the present invention are resistances mediated by ABC transporters, MDR-1, Pgp, P-glycoprotein, MRP and/or BCRP.
  • the vesicular LRP-protein does not form part of the classical ABC transporters (lung resistance-related protein).
  • the LRP promoter comprises an inverted CAAT-box (Y-box) (Scheider et al., Breast Cancer Res., 2001, 3, 183-191). Insofar also those resistances which are mediated by the vesicular LRP protein, are resistances in the meaning of the present invention.
  • viruses used in accordance with the present invention are viruses, which are YB-1 dependent, i.e. require YB-1 for replication.
  • viruses are already known in the prior art and can be used in accordance with the present invention accordingly, or that such virus can be designed based on the disclosure provided herein.
  • viruses or adenoviruses in accordance with the invention or viruses or adenoviruses used in accordance with the invention is to be understood as synonymous for the purposes of the present invention insofar that the viruses described herein may be used in accordance with the present invention provided that they use YB-1 for replicating.
  • the YB-1 used for replication can be YB-1 which is either deregulated or localized in the nucleus, in particular localized in the nucleus independent of the cell cycle, as will be outlined in the following in more detail.
  • Cells which contain YB-1 in the deregulated form are those which comprise at least one of the following characteristics and/or those which contain YB-1, whereby the YB-1 exhibits at least one of the following characteristics: (1) YB-1 is overexpressed in the cells, preferably independent of the cell cycle, whereby, preferably, as a measure for expression the expression of YB-1 in normal cells is used, i.e. cells which are different from tumour cells or cells and cell lines, respectively, such as the followings: Hepatocytes as well as fibroblast cell lines WI38 and CCD32-Lu. Preferably, there is an overexpression when the expression is increased by a factor ranging from 2 to 10, preferably from 5 to 10.
  • Methods for measuring the expression and in particular measuring the overexpression comprise, among others, measuring the protein concentration, in particular the protein concentration of YB-1, measuring RNA, in particular of YB-1, Western Blot analysis, Northern Blot analysis and RT-PCR, each preferably of or in relation to YB-1. Rather than YB-1, also surrogate markers can be used as described herein.
  • Examples for cell lines which show an overexpression of YB-1 are the followings: colon carcinoma cell line 257RDB, pancreas carcinoma cell line 181RDB, mamma carcinoma cell line MCF-7Adr, prostate carcinoma cell line DU145, prostate carcinoma cell line PC3, glioma cell line U373, glioma cell line U87, lung carcinoma cell line A549, liver carcinoma cell lines Hep3B and HepG2.
  • the YB-1 present in the cell enables the replication of the viruses in accordance with the present invention. In connection with the present invention it is preferred, when the replication efficiency under such conditions is different from a replication which is significantly reduced.
  • a significantly reduced replication is in particular a replication which is, compared to wildtype, reduced by a factor of 2, preferably by a factor of 5, more preferably by a factor of 10 and most preferably by a factor of 100.
  • comparing the replication is done by using similar or identical cell lines, similar or identical virus titres for infection (multiplicity of infection, MOI or plaque forming unit, pfu) and/or identical or similar general experimental conditions.
  • the term replication in particular refers to particle formation.
  • the extent of viral nucleic acid synthesis can be understood as measure for replication. Methods for determining the extent of viral nucleic acid synthesis are known to the one skilled in the art as well as methods for determining particle formation.
  • YB-1 A further form of deregulated YB-1 as referred to herein is phosphorylated YB-1.
  • the rational behind this is as follows.
  • YB-1 is highly expressed in quite a number of tumours and barely detectable in normal cells.
  • stress stimuli such as UV irradiation and chemotherapeutic agents (Okamoto T et al., Oncogene, 19, 6194-6202, 2000: Koike K et al., FEBS Letters, 417, 390-394, 1997).
  • Akt which is a serine/threonine kinase promotes tumor cell growth by phosphorylating transcription factors and cell cycle proteins (Nicholson K M and Anderson N G, Cell.
  • Akt phosphorylation of YB-1 by Akt weakens also its cap-binding capability, thereby facilitating translational activation of silenced mRNA species (Evdokimova V et al., Molecular and Cellular Biology, 26, 277-292, 2006). Since Akt is not active in normal cells YB-1 is not present in the phosphorylated form whereas in tumor cells YB-1 is present in “deregulated” form such as phosphorylated and/or overexpressed.
  • the various diseases and patients, respectively, to be treated using the viruses described herein and/or using the medicaments described herein, are those as described herein.
  • the timing between the administration of the viruses in accordance with the present invention and radiation or administration of the cytostatics it is to be noted that it is predominantly determined by the replication efficiency of the viruses and the kind and size of the tumour.
  • it may last some time, typically about one to three days, until the replication and thus the complexing of YB-1 and, accordingly, its non-availability for the transcription of other factors and of respective resistance causing factors in particular, occurs.
  • administration of viruses prior to any further treatment in particular administration of pharmaceutical active compounds such as pharmaceutically active agents and/or radiation, is advantageous.
  • the administration of a pharmaceutically active compound preferably comprises the administration of an anti-tumour or anti-cancer agent as disclosed herein by way of example.
  • an anti-tumour or anti-cancer agent as disclosed herein by way of example.
  • Further respective agents are known to the one skilled in the art.
  • Particularly preferred are cytostatics.
  • Exemplary cytostatics are those described herein in connection with the pharmaceutical compositions and the (pharmaceutical) agent which is administered together with the virus.
  • the dosages and treatments schemes as customary in the treatment of tumour diseases may also be applied in connection with the present invention, however, is not limited thereto.
  • the amount of the cytostatic to be administered is preferably calculated based on the body surface (as m 2 ); by means of example, the dosage of Doxorubicin is about 50 mg/m 2 .
  • the therapeutical schemes can be designed differently and comprise single day administration as well as administration of the cytostatic and radiation, respectively, for several days, weeks or even months.
  • the replication of adenoviruses is a very complex process and is usually based on the human transcription factor E2F.
  • E1, E2, E3 and E4 are expressed.
  • the group of the “late genes” is responsible for the synthesis of the structural proteins of the virus.
  • the E1 region consisting of two transcriptional units E1A and E1B which code for different E1A and E1B proteins, play a critical role for the activation of both the early and the late genes, as they induce the transcription of the E2, E3 and E4 genes (Nevins, J. R., Cell 26, 213-220, 1981).
  • the E1A proteins may initiate DNA synthesis in resting cells and thus trigger their entry into the S phase (c. f. Boulanger and Blair, 1991). Additionally, they interact with the tumor suppressors of the Rb class (Whyte, P. et al., Nature 334, 124-127, 1988). In doing so, the cellular transcription factor E2F is released.
  • the E2F factors may subsequently bind to corresponding promoter regions of both cellular and viral genes (in particular to the adenoviral E2 early promoter) and initiate transcription and thus replication (Nevins, J. R., Science 258, 424-429, 1992). The activity of pRb and E2F is regulated by phosphorylation.
  • the hypophosphorylated form of pRb particularly exists in the G1 and M phase.
  • the hyperphosphorylated form of pRb is present in the S and G2 phase.
  • E2F is released from the complex consisting of E2F and hypophosphorylated pRb.
  • the release of E2F from the complex of E2F and hypophosphorylated pRb results in transcription of E2F dependent genes.
  • the E1A protein binds only to the hypophosphorylated form of pRb, whereby the binding of E1A to pRb predominantly occurs through the CR2 region of the E1A protein.
  • the gene products of the E2 region are especially needed for the initiation and completion of the replication as they code for three essential proteins.
  • the transcription of the E2 proteins is controlled by two promoters, the “E2 early E2F dependent” promoter, which is also referred to herein as E2-early promoter or early E2 promoter, and the “E2-late” promoter (Swaminathan and Thimmapaya, The Molecular Repertoire of Adenoviruses Current Topics in Microbiology and Immunology, vol 199, 177-194, Springer Verlag 1995). Additionally, the products of the E4 region together with the E1A and E1B-55kDa protein play a crucial role for the activity of E2F and the stability of p53.
  • the E2 promoter is even more transactivated by direct interaction of the E4orf6/7 protein encoded by the E4 region with the heterodimer consisting of E2F and DP1 (Swaminathan and Thimmapaya, JBC 258, 736-746, 1996). Furthermore, the complex consisting of E1B-55kDa and E4orf6 is inactivated by p53 (Steegenga, W. T. et al., Oncogene 16, 349-357, 1998) in order to complete a successful lytic infectious cycle.
  • E1B-55kDa has a further important function insofar as it promotes, when interacting with E4orf6 protein, the export of viral RNA from the nucleus, whereas cellular RNAs are retained in the nucleus (Bridge and Ketner, Virology 174, 345-353, 1990).
  • a further important observation is that the protein complex consisting of E1B-55kDa/E4orf6 is localised in the so-called “viral inclusion bodies”. It is assumed that these structures are the sites of replication and transcription (Omelles and Shenk, J. Virology 65, 424-429, 1991).
  • the E3 region is another important region for the replication and in particular for the release of adenoviruses.
  • the E3 region more precisely contains the genetic information for a variety of comparatively small proteins which are not essential for the infectious cycle of adenovirus in vitro, i.e. in cell culture. However, they play a crucial role in the survival of the virus during an acute and/or latent infection in vivo as they have, among others, immune regulatory and apoptotic function(s) (Marshall S. Horwitz, Virologie, 279, 1-8, 2001; Russell, supra). It could be shown that a protein having a size of about 11.6 kDa induces cell death.
  • This protein was, due to its function, named ADP—for the term adenovirus death protein—(Tollefson, J. Virology, 70, 2296-2306, 1996).
  • the protein is predominantly formed in the late phase of the infectious cycle.
  • the overexpression of the protein results in a better lysis of the infected cells (Doronin et al., J. Virology, 74, 6147-6155, 2000).
  • the respective genes and proteins, respectively, are contained in the virus in accordance with the present invention.
  • virus group ⁇ 1 is described in international patent application PCT/EP/05583 published as WO 03/099859, filed on May 27, 2003 claiming the priorities of DE 102 23 534.1 of May 27, 2002, DE 102 25 400.1 of Jun. 7, 2002, DE 102 48 039.7 of Oct.
  • virus group ⁇ 2 is described in international patent application PCT/EP03/11427 published as WO 2004/035616, filed on Oct. 15, 2003 and claiming the priorities of DE 102 48 039.7 of Oct. 15, 2002, DE 103 22 530.9 of May 19, 2003, DE 103 24 085.3 of May 27, 2003 and PCT/EP03/05583 of May 27, 2003; and virus group ⁇ 3 is described in international patent application entitled “E1-minus Adenovirusen and deren severely”, filed on Jan. 2, 2006 claiming the priority of DE 10 2004 063662.1 filed on Dec. 31, 2004.
  • the term functional wildtype E1 region refers in particular to an E1 region as contained in the adenovirus Ad5 of the wildtype.
  • the term lacking functional wildtype E1 region refers to an E1 region which either does not comprise one or several functions or functionalities of the E1 region as present in wildtype adenoviruses or which does not completely comprise the same.
  • the functionality or function in the following generally referred to as function, is mediated by a nucleic acid or a protein, preferably is represented or mediated by a protein.
  • the lack of function can be caused by the function not being active at the level of translation, i.e. that the function mediating protein is not present although the nucleic acid coding therefore is still present in the viral genome.
  • This can, for example, be caused by the regulatory elements controlling its translation being absent, such as, for example, the 3′UTR of the mRNA which, among others, provide for the stability of the mRNA.
  • these regulatory elements are no longer present in the regulatory and controlling context as present in wildtype viruses for the respective function.
  • the lack of function can, alternatively or additionally, be caused by the function not being active at the level of transcription, i.e. that the protein mediating the function is not present and the nucleic acid coding therefore, is not contained in the viral genome or not completely contained in the viral genome.
  • the coding nucleic acid comprises one or several mutations which result in the loss of function. Such mutations are preferably point mutations and/or deletions comprising several bases and/or a complete deletion of the open reading frame or the nucleic acid coding for the protein.
  • a function is lacking in the sense of the above embodiments if the protein does not comprise all functions or activities as exhibited by the corresponding wildtype protein.
  • the extent of replication is used as a measure for activity which can be obtained under such conditions, whereby it is preferably significant different from a replication using the wildtype protein, genotype and/or phenotype.
  • a different regulatory context is in a preferred embodiment a context in connection with which the function is, compared to other functions, expressed at a different point in time and/or is under the control of a different transcription and/or translation controlling or influencing element. Such an element is in a particular embodiment the promoter.
  • a strongly reduced replication herein in particular means a replication which is decreased compared to the wildtype by a factor of 2, preferably a factor of 5, more preferably a factor of 10 and most preferably a factor of 100.
  • the comparison of the replication is made using identical or similar cell lines, identical or similar virus titres for the infection (multiplicity of infection, MOI or plaque forming unit, pfu) and/or identical or similar general experimental conditions.
  • Replication particularly means the formation of particles.
  • the measure for replication may be the extent of viral nucleic acid synthesis. Methods for determining the extent of viral nucleic acid synthesis and methods for the determining particle formation are both known to the ones skilled in the art.
  • E1A-modified adenoviruses are adenoviruses which (a) do not replicate in YB-1 nucleus-negative cells or show a reduced, preferably a strongly reduced replication in YB-1 nucleus-negative cells compared to the respective wildtype, (b) transactivate at least one viral gene, whereby the gene is in particular selected from the group comprising E1B-55kDa, E4orf6, E4orf3 and E3ADP, and/or (c) do not translocate cellular YB-1 through the adenovirus into the nucleus.
  • the adenoviruses used in accordance with the present invention have the further characteristic that the binding of the adenoviral encoded E1A protein interferes with the binding of E2F to Rb and is able to dissolve the respective complex consisting of E2F and Rb, respectively.
  • Adenoviruses which have at least one or several of the aforementioned features a) to c), preferably all of features a) to c), are replication deficient in cells which do not have YB-1 in the nucleus.
  • the E2-early promoter i.e. the early E2 promoter which is controlled by the E2F transcription factor
  • the switching on of the replication is independent of the Rb status of the cells, i.e. which means that the tumor cells which are infected using the viruses disclosed herein and which are preferably lysed subsequently thereafter, may comprise both functional as well as inactive Rb proteins.
  • adenoviral replication does neither need any functional p53 protein nor is it affected by its presence, when using the adenoviruses disclosed herein or under the conditions disclosed herein.
  • the technical teaching departs from the principle underlying the use of the oncolytic or tumorlytic adenoviruses of the Ad ⁇ 24, dl922-947, E1Ad/01/07, CB016 type or of those adenoviruses which are, for example, described in European patent EP 0 931 830, and into which one or several deletions have been introduced into the E1A protein under the assumption that intact functional Rb proteins are an obstacle to an efficient replication in vivo thus providing an adenoviral replication in vivo only in Rb-negative and Rb-mutated cells, respectively.
  • adenoviral systems according to the prior art are based on E1A in order to control in vivo replication of adenoviruses by means of the early E2 promoter (E2 early promoter) and “free E2F”. Nevertheless, these viruses according to the prior art may be used in accordance with the present invention, i.e. for replication in cells which contain YB-1 in the nucleus independent from the cell cycle.
  • viruses described in said European patent EP 0 931 830 and in particular adenoviruses may be used in accordance with the present invention. More particularly, the viruses described in said patent are replication deficient and lack an expressed viral oncoprotein which is capable of binding a functional Rb tumor suppressor gene product.
  • the adenovirus can particularly be an adenovirus which is lacking expressed viral E1A oncoprotein which is capable of binding a functional tumor suppressor gene product, in particular Rb.
  • the viral E1A oncoprotein can comprise an inactivating mutation, for example in the CR1 domain at amino acid positions 30 to 85 in Ad 5, nucleotide positions 697 to 790 and/or the CR2 domain at amino acid positions 120 to 139 in Ad 5, nucleotide positions 920 to 967 which are involved in the binding of p105 Rb protein, p130 and p107 protein. It can also be intended that the adenovirus is of type 2 dl 312 or the adenovirus is of type 5 NT dl 1010.
  • a further feature of the adenoviruses which are to be used in accordance with the present invention is that they code for a viral oncoprotein which is also referred to herein as oncogene protein, whereby the oncogene protein is preferably E1A, whereby the oncogene protein is capable of activating at least one viral gene which can have an impact on the replication of the virus and/or cell lysis of the cells infected by the virus. It is preferred that the influence on replication is such that the virus replicates better in the presence of the oncogene protein compared to a situation where the oncogene protein of the respective virus is lacking.
  • transactivate describes preferably the process that the respective viral oncoprotein has an impact on the expression and/or the transcription of one or several other genes different from the viral oncoprotein coding gene itself, i.e. is preferably controlling its expression and/or translation, and in particular activates this/these.
  • viral genes are preferably E1B55kDa, E4orf6, E4orf3 and E3ADP as well as any combination of the aforementioned genes and gene products, respectively.
  • the adenoviruses used in accordance with the present invention bind to Rb or do not bind to Rb.
  • the use of both alternative embodiments of the adenoviruses is possible independently from the Rb status of the cell to be treated.
  • the following deletions of the E1A oncoprotein are, for example, possible: Deletion in the CR1 region (amino acid positions 30-85 in Ad5) and deletion of the CR2 region (amino acid positions 120-139 in AD5). In doing so, the CR3 region is maintained and can have its transactivating function on the other early viral genes.
  • deletions to the E1A oncoprotein are in principle possible in order to impart E1A the capability to bind to Rb: deletion of the CR3 region (amino acid positions 140-185); deletion of the N-terminus (amino acid positions 1-29); deletion of amino acid positions 85-119; and deletion of the C-terminus (amino acid positions 186-289).
  • the regions recited herein do not interfere with the binding of E2F to Rb.
  • the transactivating function remains, however, is reduced compared to wildtype Ad5.
  • the modified E1A oncoprotein of the various adenoviruses which are to be used in accordance with the invention, is capable of transactivating the early viral genes such as, for example, E1B55K, E4orf3, E4orf6, E3ADP, in YB-1 nucleus-positive cells.
  • the respective adenovirus can otherwise correspond to an adenovirus of the wildtype or any derivative thereof.
  • viruses disclosed herein which code for a transactivating oncogene protein in the sense of the present invention or which comprise such oncogene protein comprise, for example, the adenoviruses Ad ⁇ 24, dl922-947, E1Ad/01/07, CB106 and/or the adenoviruses described in European patent EP 0 931 380, which are each capable of transactivating the early genes, such as E1B, E2, E3 and/or E4, and are comparable to adenoviruses of the wildtype, in particular wildtype Ad5.
  • a particular region of the E1A protein is responsible for transactivation in these cases.
  • Within various adenovirus serotypes there are three highly conserved regions in the E1A protein.
  • the transactivating function is primarily based on the presence of the CR3 region in the E1A protein.
  • the amino acid sequence of CR3 is unaltered in the aforementioned adenoviruses. This results in a transactivation of the early genes E1B, E2, E3 and E4 independent from the presence of YB-1 in the nucleus or in the cytoplasma.
  • dl520 expresses a so-called E1A12S protein which does not comprise the amino acid sequence of the CR3 region.
  • E1A12S protein which does not comprise the amino acid sequence of the CR3 region.
  • dl520 can exert a very weak transactivating function only, in particular on the E2 region, and thus does not replicate in YB-1 nucleus-negative cells.
  • YB-1 nucleus-positive cells YB-1 is transactivating the E2 region and thus allows an efficient replication of dl520. This is the basis for the use of systems like dl520 and of systems on the basis of dl520 for the purposes disclosed herein, respectively.
  • delta 24 (herein also referred to as Ad ⁇ 24) and dl520 resides in the fact that with dl520 the early genes E1B, E3 and E4 are more strongly transactivated in YB-1 nucleus-positive cells compared to YB-1 nucleus-negative cells. In contrast, there are no or only minor differences with delta 24.
  • the transactivation effect of dl520 and more particularly of the E1A12S protein, however, is significantly reduced compared to wildtype adenovirus. This transactivation is, however, sufficient in order to allow for an efficient replication in YB-1 nucleus-positive cells, as shown in example 10.
  • adenoviruses which are to be newly constructed typically have an E1 deletion, an E1/E3 deletion and/or an E4 deletion, i.e.
  • the corresponding adenoviruses are not able to generate functionally active E1 and/or E3 and/or E4 expression products and respective products, respectively, or, in other words, these adenoviruses are only capable to generate functional inactive E1, E3 and/or E4 expression products, whereby a functionally inactive E1, E3 and/or E4 expression product as such which is either not present as an expression product at all, whether at the transcription level and/or the translation level, or it is present in a form in which it at least is lacking one of the functions it has in wildtype adenoviruses.
  • the function(s) of the expression product of the wildtype adenovirus is/are known to the ones skilled in the art and, for example, described in Russell, W.
  • the individually named genes as well as the transgenes disclosed herein can be cloned into the E1 and/or E3 and/or E4 region and be expressed independently by virtue of a suitable promoter or under the control of a suitable promoter.
  • the regions E1, E3 and E4 are similarly suitable as cloning sites within the adenoviral nucleic acid, whereby the regions which are not used for the cloning may, either individually or all together, be present, partially deleted and/or completely deleted.
  • Suitable promoters are, for example those, which are disclosed herein in connection with the control and expression, respectively, of E1A, in particular of modified E1A.
  • the adenoviruses which are to be used in accordance with the present invention are deficient with regard to E1B, in particular with regard to E1B 19 kDa.
  • the term deficient generally means a condition in which E1B does not have all of the characteristics inherent to the wildtype but at least one of these characteristics is absent.
  • the adenoviral BCL2 homologue E1B19k inhibits the E1A induced apoptosis by interacting with the pro-apoptotic proteins Bak and Bax. Because of this, a maximum replication and/or particle formation is possible in infected cells (Ramya Sundararajan and Eileen White, Journal of Virology 2001, 75, 7506-7516).
  • E1B19k results in a better release of the viruses as it minimizes the function of the adenoviral death-protein, if present.
  • the virus induced cytophatic effect is increased by such deletion (Ta-Chiang Liu et al., Molecular Therapy, 2004) and thus results in a stronger lysis of the infected tumour cells.
  • the lack of E1B19k results in TNF-alpha not having an impact on the replication of such recombinant adenovirus in tumour cells, whereas in normal cells the treatment results in a reduced replication and release of infectious viruses.
  • the selectivity and specificity is increased (Ta-Chiang Liu et al., Molecular Therapy 2004, 9, 786-803).
  • adenoviruses which are used in accordance with the invention disclosed herein, are, basically, known in the prior art.
  • the adenoviruses used in accordance with the present invention are preferably recombinant adenoviruses, particularly also when a change, compared to the wildtype, has been made in accordance with the technical teaching provided herein. It is within the skills of those of the art to delete or mutate those adenoviral nucleic acid sequences which are not essential for the present invention. Such deletions may, for example, be related to a part of the nucleic acid coding for E3 and E4 as also described herein. A deletion of E4 is particularly preferred if such deletion does not extend to the protein E4orf6, or, in other words, the adenovirus to be used in accordance with the present invention codes for E4orf6.
  • these adenoviral nucleic acids may still be packed into the viral capsid and may thus form infectious particles. The same is true for the use of the nucleic acids in accordance with the present invention. It should be noted that in general the adenoviral systems may be deficient with regard to single or several expression products.
  • this may be either based on the fact that the nucleic acid coding for such expression product is completely mutated or deleted or mutated or deleted to the extent that essentially no expression product is produced anymore or based on the lack of promoters or transcription factors which control the expression, or which are active in a manner different from wildtype, either at the nucleic acid level (lack of a promoter; cis-acting element) or at the translation system and the transcription system, respectively (trans-acting elements). Particularly the latter aspect may be dependent on the cellular background.
  • novel adenoviruses can be used to the same extent as has already been disclosed for the other adenoviruses described herein.
  • the novel adenoviruses according to the invention result from the technical teaching provided herein.
  • Particularly preferred representatives are, for example, the viruses Xvir03 and Xvir03/01 depicted in FIG. 16 and FIG. 17 , the design principle of which is also further illustrated in examples 11 and 12.
  • a CMV promoter is cloned into the E1 region which codes the nucleic acids for E1B 55K and E4ORF6, which are separated by a IRES sequence.
  • the E3 region can be partially or completely be deleted or can be present and intact. Due to the introduction of these two genes and the gene products produced therefrom, respectively, a replication efficiency is created which nearly corresponds to the one of wildtype viruses, whereby the selectivity of the replication is maintained for cells, particularly tumor cells, insofar as a replication happens in particular in YB-1 nucleus-positive cells and more particularly in cells in which YB-1 is deregulated.
  • Cells in which YB-1 is deregulated are preferably those which show an increased expression of YB-1, preferably compartment-independent, compared to normal or non-tumor cells.
  • the introduction of E1B55k and E4orf6 into the E4-region by cloning can also be performed, whereby the E3 region may be intact or/and partially or completely deleted.
  • virus Xvir03/01 into which, in a preferred embodiment, therapeutic genes or transgenes are cloned under the control of a specific promoter, in particular a tumor-specific or tissue-specific promoter. It is also within the scope of such a virus that also the E4 region is functionally inactive, preferably is deleted.
  • the transgenes described here in may also be cloned into the E4 region, whereby this may occur in addition or alternative to the cloning of a transgene into the E3 region, and the E3-region remains partially or completely intact.
  • Transgenes may be therapeutic genes or viral genes, preferably adenoviral genes, which are preferably not present in the genome of the wildtype adenovirus or at the position in the genome, respectively, where they are present in the particular virus now.
  • the adenoviral nucleic acid is deficient for the expression of the oncogene protein, particularly of the E1A protein, which means that it is either not coding for the 12S E1A protein or for the 13S E1A protein, or it is neither coding for the 12S E1A protein nor the 13S E1A protein, or is modified, as defined herein, and that the adenoviral replication system further comprises a nucleic acid of a helper virus, whereby the nucleic acid of the helper virus comprises a nucleic acid sequence which codes for the oncogene protein, in particular for the E1A protein, which has the following characteristics and imparts the following characteristics to the adenovirus, respectively, namely that it preferably is not replicating in YB-1 nucleus-negative cells but in cells which are independent from the cell
  • viruses are categorized, again for reason of clarity, into group I and group II.
  • the viruses first defined in the claims related to virus group ⁇ 2 are also referred to herein as adenovirus of group I, and the adenoviruses which comprise a transactivating oncogene protein such as E1A and/or those which are referred to herein and in particular above as to be used in accordance with the present invention, are also referred to herein as adenovirus of group II.
  • Adenovirus of group I and group II are all together also referred to herein as adenoviruses or adenoviruses in accordance with the invention or viruses in accordance with the present invention. Again, it is within the present invention that, preferably, any feature, embodiment and/or use described herein in relation to group I is also applicable to group II and vice versa.
  • viruses are based on the surprising finding that reversing the expression sequence of adenoviral genes results in an efficient replication and optionally in the lysis of the cell infected by the adenovirus.
  • reversing is a chronological reversing of expression and/or availability of the genes and gene products, respectively, compared to the expression and/or availability order of the respective genes in wildtype virus, preferably wildtype adenovirus.
  • chronologically changed expression of the adenoviral genes particular emphasis is to be put on an E1B protein and an E4 protein which are also referred to herein, individually or collectively, as the first protein, which are expressed prior to a second protein.
  • the second protein is selected from the group comprising E1A proteins.
  • This expression sequence which is reversed compared to wildtype adenoviruses where first an E1A protein and only subsequently the MB protein and an E4 protein are expressed, ensures that transcription factors are activated, for example transported, into the nucleus of the infected cell and influence the further replication activity or control the same there.
  • the kinetics of the adenoviral transcripts in wildtype adenoviruses are, for example, described in Glenn G. M. and Ricciardi R. P. Virus Research 1988, 9, 73-91, who report that in the wildtype the E1A transcripts, i.e.
  • the E1A12S transcript and the E1A13S transcript are usually detectable prior to the transcripts and translation products, respectively, E4orf6 and E1B55k.
  • the E1B protein is, and also herein in general if not indicated to the contrary, preferably the E1B-55kD protein.
  • the E4 protein is, and also herein in general if not indicated to the contrary, preferably the E4orf6 protein.
  • the E1A protein is, and also herein in general if not indicated to the contrary, preferably an E1A12S protein or such an E1A protein as described herein in connection with the E1A-modified adenoviruses.
  • E1A protein in particular also the E1A12S protein may be substituted in principle.
  • substituted E1A proteins and E1A12S proteins, respectively are also referred to herein as E1A protein and E1A12S protein, respectively, or shall be deemed to be comprised by this term, if not indicated to the contrary.
  • E1A12S protein also an E1A protein may be used which has a tumor suppressor function, such as, for example, described by Dickopp A, Esche H, Swart G, Seeber S, Kirch H C, Opalka B. Cancer Gene Ther. 2000, July; 7(7):1043-50.
  • E1A proteins in particular of the E1A12S protein, as used and/or as referred to as such herein, are generally also such proteins which are capable of releasing the factor E2F from the Rb/E2F complex.
  • Simian virus 40 tumor antigen SV40 large T antigen
  • HPV E7 papillomavirus E7 protein
  • E4orf6 and E1B55k may be used, whereby the term E4orf6 and E1B55k, as used herein, comprises such derivatives.
  • the derivatives are, for example, described in Shen Y et al., J. of Virology 2001, 75, 4297-4307; Querido E. et al., J. of Virology 2001, 75, 699-709.
  • an E1B protein is expressed prior to the E1A protein, or that an E4 protein is expressed prior to an E1A protein, or that both an E1B protein and an E4 protein are expressed prior to the E1A protein, each as described above.
  • An adenovirus designed in such a way is capable of replicating at a particularly high level upon infection of a cell which expresses YB-1 in the nucleus, preferably expresses YB-1 in the nucleus independent from the cell cycle, or which comprises deregulated YB-1, preferably in the cytoplasm.
  • a complex consisting of E1B protein and/or E4 protein and individual ones of these two proteins, respectively is/are capable of transporting deregulated YB-1 into the cellular nucleus or is/are capable of initiating adenoviral replication there under the influence of the E1B protein and/or E4 protein being expressed prior to the E1A protein.
  • YB-1 may, as described herein, in particular using the E2-late promoter, efficiently replicate.
  • the chronologically early expression of an E1B protein and/or an E4 protein thus avoids the cascade as observed in wildtype going along with initial expression of E1A protein.
  • the E1A protein is an E1A protein which is in particular no longer transactivating or transactivating only to a very limited extent the E1B protein and/or the E4 protein.
  • this transactivation is neither sufficient to ensure an efficient replication, nor sufficient to ensure replication in cells which do not have YB-1 in the nucleus. It is preferred that the transactivation does not occur in cells which do not have YB-1 in the nucleus independent from the cell cycle or cells which do not have deregulated YB-1.
  • an adenovirus is capable of replicating in a particularly efficient manner if it comprises at least a nucleic acid which codes for a protein, whereby the protein is selected from the group comprising E1B proteins, E4 proteins and E1A proteins and that at least one protein thereof is under the control of a promoter which is different from the promoter which controls the expression of the respective protein in a wildtype adenovirus.
  • Such replication is particularly efficient and usually results in tumor lysis in case the cells have YB-1 in the nucleus, in particular have YB-1 in the nucleus independent of the cell cycle, or in case the cells comprise deregulated YB-1, in particular comprise deregulated YB-1 in the cytoplasm.
  • E1B proteins, E4 proteins and E1A proteins applies also here.
  • the E1B protein is controlled by the E1B promoter
  • the E4 protein is controlled by the E4 promoter
  • the E1A protein is controlled by the E1A promoter.
  • the mechanism may be the one as already previously described with regard to the chronologically different expression of the adenoviral proteins E1B, E4 and E1A.
  • An example of a specific design for the control of said proteins through promoters different from those controlling the expression of the respective proteins in wildtype adenovirus, may be taken from the sub-claims and from the example part, whereby in particular the viruses referred to therein as XVirPSJL1 and XVirPSJL2 are representative thereof.
  • the E1B protein is the E1B55kD protein
  • the E4 protein is the E4orf6 protein
  • the E1A protein is the E1A12S protein.
  • the promoters which preferably control the E1B protein as well as the E4 protein are selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters under the proviso that when adenoviral promoters are used, they are different from the E1B promoter in case of the expression control of the E1B protein, and are different from the E4 promoter in case of expression control of the E4 protein.
  • the use of the E1A promoter for the expression control of the E1B protein and/or the E4 protein is particularly preferred.
  • the E1A promoter is, for example, described by Boulanger P. A. and Blair, G. E. Biochem. J.
  • each and any other heterologous promoter is possible, i.e. a promoter which is different from the one which controls the expression of the respective protein in a wildtype adenovirus.
  • a representative example is the CMV promoter, whereby other promoters will be obvious for the ones skilled in the art.
  • the promoter which is used for the control of the E1A protein may also be selected from the group comprising tumor-specific promoters, organ-specific promoters, tissue-specific promoters, heterologous promoters and adenoviral promoters under the proviso that the adenoviral promoter is different from the E1A promoter. It is within the present invention that one or several of the aforementioned proteins, i.e. the E1B protein, the E4 protein or the E1A protein are under the control of the same promoter, whereby it is nevertheless preferred that particularly the E1B protein and the E4 protein are under the control of the same promoter.
  • the expression of the E1A protein is controlled by a YB-1-controlled promoter or a promoter which can be regulated by YB-1.
  • a YB-1-controlled promoter or a promoter which can be regulated by YB-1 Such promoters are disclosed herein in connection with other aspects of the present invention.
  • the use of the adenoviral E2-late promoter is particularly preferred for the control of the expression of the E1A promoter as it can, first, be regulated by YB-1 and, second, shows only little transcription in the absence of YB-1 which can factually be neglected so that a very good expression control of the nucleic acid which is under the control of the E2-late promoter, is ensured.
  • YB-1 dependent or YB-1 controlled promoters can be used insofar which are either known to the ones skilled in the art or described herein. This considerably increases biological safety, particularly when applied in the field of medicine.
  • adenoviruses will replicate particularly well in cells which have YB-1 in the nucleus, particularly have YB-1 in the nucleus independent of the cell cycle, and/or which have deregulated YB-1, preferably have deregulated YB-1 in the cytoplasm, if YB-1 is provided for replication either directly or indirectly in particular in the cellular nucleus or if the provision of YB-1 is directly or indirectly mediated through an adenoviral protein, whereby such adenoviral protein is different from E1A.
  • This aspect of the present invention is different from the aspect which is also disclosed herein, namely that the use of transactivating E1A-modified adenoviruses, preferably group II adenoviruses, allows for replication of these viruses in YB-1 nucleus-positive tumor cells, particularly YB-1 nucleus-positive cells which are YB-1 positive independent of the cell cycle, and those cells which have deregulated YB-1, particularly comprise YB-1 in the cytoplasm, insofar that the transactivating characteristics of the E1A protein, particularly the E1A13S protein are not used here, i.e.
  • the E1A13S protein is functionally inactive and is thus no longer capable of transactivating also E4orf6 and E1B55k, which are involved in the transport and provision of YB-1, respectively, into the nucleus, either directly or indirectly. Consequently, an effective replication of the adenovirus is not possible in accordance with this aspect of the present invention.
  • This embodiment of the adenovirus may also be provided by one of the above-described measures, for example by realizine, i.e. bringing forward, the earlier chronological expression of the E1B protein and/or the E4 protein compared to the expression of the E1A protein, or by putting one or several of the E1B proteins, E4 proteins and E1A proteins under the control of a promoter which is different from the promoter which controls the expression of the respective protein in wildtype adenovirus.
  • an effective adenoviral replication may also occur, particularly in cells which have YB-1 in the nucleus, more particularly YB-1 in the nucleus independent of the cell cycle, or in cells which have deregulated YB-1, preferably in the cytoplasm, in case at least one of the MB proteins, E4 proteins and E1A proteins, particularly the preferred forms thereof, are expressed in an expression cassette under the control of a promoter.
  • the present invention basically three expression cassettes each comprising a single one of said proteins are provided.
  • an expression cassette may also comprise two or more of the proteins E1B, E4 and E1A and their derivatives and possible substituents, respectively, particularly in case of E1A12S.
  • the adenoviruses comprise nucleic acids related to proteins E1B, E4 and E1A, is also applicable to the design of the various proteins and the respectively used promoters.
  • proteins and nucleic acids coding therefor in the genome of the wildtype adenovirus which correspond to the respective proteins of the expression cassettes are either completely or partially deleted to ensure that the virus is stable and to avoid recombinations, at least to a bigger extent.
  • the expression cassettes can be cloned into each region and each site, respectively, of the adenovirus, whereby preferably one or several of the cassettes are inserted either individually or in combination with each other into the E1 region, the E3 region and/or the E4 region of the virus. It is possible that the nucleic acids of the E1, E3 and E4 region are completely deleted, partially deleted or not deleted at all, whereby it is preferred with regard to the adenoviruses according to the invention that the nucleic acid coding for the E1A13S gene is inactivated or deleted so as not to provide any transactivating E1A protein by the virus.
  • the extent of such deletion in one or several of the regions E1, E3 and E4 is determined by the expression cassette used and, optionally, further introduced foreign genes or transgenes or the further expression cassettes comprising them, i.e. genes which are different from the adenoviral genes, at least different in the sense that they are not provided in the regulatory context of the adenoviral nucleic acid as prevailing in wildtype adenovirus or are not provided in the sequence of the adenoviral nucleic acids of wildtype adenoviruses at such site.
  • the nucleic acids which are contained in one or several of the expression cassettes which code for an E1B protein, an E4 protein and/or an E1A protein are partially or completely deleted in the adenoviral genome.
  • the adenoviral nucleic acid coding for E4orf6 is partially or completely deleted, however, the complete nucleic acid coding therefor is contained in the expression cassette.
  • this will also be realised for the E1 B55k (also referred to as E1 55Kd) protein and/or the E1A12S protein.
  • the extent of the deletion is to be selected in preferred embodiments such that a maximum package size of about 103% of the maximum package size of the wildtype adenovirus is reached, although this limit is only a preferred limit.
  • the possible deletions to be made in the adenoviral genome are only subject to limitations in preferred embodiments such as to make sure that still infectious and packed particles can be manufactured.
  • the precise extent of the deletions may be determined by the ones skilled in the art on the basis of the disclosure provided herein together with standard tests.
  • any wildtype adenovirus may be used, but also other adenoviruses may be used provided that they are constructed in accordance with the technical teaching of the present invention. It is particularly preferred to have recourse to adenoviruses of subgroup C and within this group in turn to adenovirus 2 and adenovirus 5.
  • E1B protein and E1B proteins, E4 protein and E4 proteins as well as E1A protein and E1A proteins are used herein in a synonymous manner, if not indicated to the contrary.
  • the term “deregulated” YB-1 refers to a YB-1 molecule or YB-1 protein as described herein which is present in a form which is quantitatively and/or qualitatively different from YB-1 as normally present in cells, preferably in non-tumor cells.
  • a deregulated YB-1 can be characterised and identified as such by particular viruses being able to replicate in the presence of deregulated YB-1 in a cellular background comprising such deregulated YB-1.
  • the particular viruses in connection therewith are those the E1A protein of which is mutated and exhibits a transactivating function. Examples for these particular viruses are AD delta 24, dl 922-947, E1 Ad/01/07 and CB 016 and/or those described by Howe, J.
  • Such a cell and a cell, respectively, having such a background can be used for the replication of group I adenoviruses and/or group II adenoviruses. Additionally, tumors comprising such cells may be lysed by the adenoviruses according to the invention.
  • E1A-modified adenoviruses are to be understood as those which (a) have, in YB-1 nucleus-negative cells, a reduced or no replication at all compared to wildtype, (b) have a transactivation activity on at least one viral gene, whereby the gene is particularly selected from the group comprising E1B-55kDa, E4orf6, E4orf3 and E3ADP, and/or (c) do not translocate cellular YB-1 into the nucleus by the adenovirus.
  • the adenoviruses used in accordance with the present invention have the further characteristic that the binding of the E1A protein encoded by the adenovirus is interfering with the binding of E2F to RB and is capable of dissolving the respective complex consisting of E2F and Rb.
  • Adenoviruses which have one or several of the aforementioned features a) to c), preferably all of the features a) to c), are replication deficient in cells which do not have YB-1 in the nucleus.
  • the present inventor assumes that the adenoviral E2 expression is not switched on to a sufficient manner by the E2-early promoter, i.e. the early E2 promoter, through the human cellular E2F transcription factor in connection with the replication of the viruses used in accordance with the present invention and in connection with the use in accordance with the present invention of the adenoviruses disclosed herein.
  • the start of the replication is independent of the Rb status of the cells, i.e. the tumor cells which are infected by using the viruses disclosed herein and which are preferably lysed subsequently, may contain either functional as well as inactive Rb proteins.
  • adenoviral replication using the adenoviruses disclosed herein or using the conditions disclosed herein does not require any functional p53 protein, however is neither negatively affected by its presence.
  • the technical teaching turns away from the principle underlying the use of oncolytic or tumorlytic adenoviruses of the type of Ad ⁇ 24, dl922-947, E1Ad/01/07, CB016 or those adenoviruses described, for example, in European patent EP 0 931 830, which had been made subject to one and/or several deletion(s) in the E1A protein under the assumption that intact functional Rb proteins would hinder an efficient in vivo replication and thus provide for adenoviral replication in vivo only in Rb-negative and Rb-mutated cells.
  • adenoviral systems of the prior art are based on E1A in order to control in vivo replication of adenoviruses by means of the early E2 promoter (E2-early promoter) and “free E2F”. Nevertheless, these known viruses of the prior art may be used in accordance with the present invention for the replication in cells which contain YB-1 in the nucleus independent of the cell cycle, or in cells which comprise deregulated YB-1.
  • viruses in particular adenoviruses described in said European patent EP 0 931 830 may be used in accordance with the present invention. More specifically, the viruses described in said patent are viruses which are replication deficient and which lack an expressed viral oncoprotein which is capable of binding a functional Rb tumor suppressor gene product.
  • the adenovirus can particularly be any adenovirus which lacks expressed viral E1A oncoprotein which is capable of binding a functional tumor suppressor gene product, more particularly Rb.
  • the viral E1A oncoprotein can exhibit an inactivating mutation, for example in the CR1 domain at the amino acid positions 30 to 85 in adenovirus Ad5, which is also referred to herein as Ad5, Ad 5, the nucleotide positions 697-790 and/or the CR2 domain at amino acid positions 120 to 130 in Ad 5, the nucleotide position 920 to 967 which are involved in the binding of p105 Rb protein, p130 and p107 protein.
  • Ad5 adenovirus
  • Ad5 the nucleotide positions 697-790 and/or the CR2 domain at amino acid positions 120 to 130 in Ad 5
  • the nucleotide position 920 to 967 which are involved in the binding of p105 Rb protein, p130 and p107 protein.
  • the adenovirus is of type 2 dl 312 or type 5 NT dl 1010.
  • a further feature of a part of the adenoviruses to be used in accordance with the present invention which are different from other adenoviruses of the present invention, is that they code for a viral oncogene which is also referred to herein as oncogene protein, whereby the oncogene protein is preferably E1A and whereby the oncogene protein is capable of activating at least one viral gene which has an impact on the replication of the virus and/or cell lysis of the cell infected by said virus.
  • the impact on the replication is such that the virus replicates better in the presence of the oncogene protein compared to the scenario where the oncogene protein of the respective virus is absent.
  • transactivating preferably describes the process that the respective viral oncoprotein has an impact on the expression and/or on the transcription of one or several other genes which are different from the gene coding for the viral oncogene protein itself, i.e. controls its/their expression and/or translation and particularly activates it/them.
  • viral genes are preferably E1B55kDa, E4orf6, E4orf3 and E3ADP as well as any combination of the aforementioned genes and gene products, respectively.
  • a further, although only optional feature of the adenoviruses to be used in accordance with the present invention as well as of the adenoviruses of the present invention is their binding characteristics and the binding characteristics of particular ones of the proteins coded by them, respectively, to tumor suppressor Rb. Basically, it is within the present invention that the adenoviruses used in accordance with the present invention may or may not bind to Rb.
  • the use of any of the two alternative embodiments of the adenoviruses is independent of the Rb status of the cells treated or the cells to be treated.
  • deletions can be made to the E1A oncoprotein: deletion in the CR1 region (amino acid positions 30-85 in Ad5) and deletion of the CR2 region (amino acid positions 120-139 in Ad5). In doing so, the CR3 region is preserved and can exercise its transactivating function on the other early viral genes.
  • deletions to E1A oncoprotein are basically possible: deletion of the CR3 region (amino acid positions 140-185); deletion of the N-terminus (amino acid positions 1-29); deletion of the amino acid positions 85-119; and deletion of the C-terminus (amino acid positions 186-289).
  • the regions listed above do not interfere with the binding of E2F to Rb.
  • the transactivating function remains intact, however, is reduced compared to wildtype Ad5.
  • the E1A protein, particularly the E1A12S protein is designed such that, in an embodiment, it is capable of binding to Rb and, in a different embodiment, is not capable of binding to Rb, whereby such E1A12S protein is an E1A protein and particularly an E1A12S protein in the meaning of the present invention which is nevertheless referred to in the prior art sometimes as modified E1A12S.
  • the respective design of the E1A12S protein is within the skills of those of the art, particularly with regard to the aforementioned deletions of the E1A protein which is also referred to herein simply as E1A.
  • Such adenoviruses which are basically already known in the prior art and which do not show any transactivation, are generally regarded as replication deficient. However, it is the merit of the present inventor that he has recognised that such viruses are nevertheless capable of replicating in a suitable background, in particular a suitable cellular background.
  • suitable cellular background is caused or provided by the presence of YB-1 in the nucleus, preferably a cell cycle independent presence of YB-1 in the nucleus, or by deregulated YB-1.
  • the term cells or cellular systems as used herein in connection with each and any other aspect of the present invention comprises fragments or fractions of cell extracts as well as cells which are present in vitro, in vivo or in situ.
  • the term cellular systems or cells also comprises cells which are present in cell culture, tissue culture, organ culture or in any tissue or organ in vivo and in situ, respectively, isolated, in groups or as part of tissues, organs or organisms, but which may also be present as such in a preferably living organism.
  • the organism is preferably any vertebrate organism and more preferably a mammal. More preferably the organism is a human organism. Other preferred organisms are those disclosed in connection with the various aspects of the present invention.
  • the modified E1A oncoprotein of the various adenoviruses to be used in accordance with the present invention is capable of transactivating the early viral genes such as E1B55K, E4orf3, E4orf6, E3ADP in YB-1 nucleus-positive cells or cells which comprise deregulated YB-1.
  • the respective adenovirus may insofar correspond otherwise to a wildtype adenovirus or a derivative thereof.
  • viruses disclosed herein which code or comprise a transactivating oncogene protein in the meaning of the present invention, comprise, for example, the adenoviruses Ad ⁇ 24, dl922-947, E1Ad/01/07, CB106 and/or the adenoviruses described in European patent EP 0 931 830 which are each capable of transactivating the early genes such as E1B, E2, E3 and/or E4 and which are comparable to the adenoviruses of wildtype, particularly wildtype Ad5.
  • a distinct region of the E1A protein is responsible for the transactivation.
  • Within the various adenoviral serotypes there are three highly conserved regions within the E1A protein.
  • the transactivating function is mainly based on the presence of the CR3 region within the E1A protein.
  • the amino acid sequence of CR3 is present in an unchanged manner in the above mentioned adenoviruses. This results in a transactivation of the early genes E1B, E2, E3 and E4 independent of whether YB-1 is present in the nucleus or in the cytoplasm.
  • dl520 expresses a so-called E1A12S protein which does not comprise the amino acid sequence of the CR3 region. Consequently, dl520 may exercise only a very weak transactivating function, particularly on the E2 region, and thus does not replicate in YB-1 nucleus-negative cells. In YB-1 nucleus-positive cells YB-1 is responsible for the transactivation of the E2 region and thus allows for an efficient replication of dl520.
  • the use of systems like dl520 or systems originating therefrom for the purposes disclosed herein, is based thereon.
  • delta 24 also referred to herein as Ad ⁇ 24
  • dl520 resides in the fact that the early genes E1B, E3 and E4 are more comprehensively transactivated in cells being YB-1 nucleus positive cells independent of the cell cycle or in cells containing deregulated YB-1, compared to YB-1 nucleus-negative cells or cells which do not comprise deregulated YB-1. In contrast thereto, there are no or only minor differences in delta 24.
  • the transactivation of dl520, more specifically of the E1A12S protein is, however, significantly reduced compared to wildtype adenovirus.
  • the deletion is such that it is selected from the group comprising deletions of the CR3 region and deletions of the N-terminus and deletions of the C-terminus.
  • Further embodiments of the E1A protein which allow this kind of replication of adenoviruses can be generated by the ones skilled in the art based on the disclosure provided herein.
  • the embodiment of the E1A protein as described previously is an embodiment which may also be used in connection with the adenoviruses of the present invention which are also referred to herein as adenoviruses of the present invention or group I adenoviruses.
  • the adenoviruses of the present invention typically comprise an E1 deletion, an E1/E3 deletion and/or an E4 deletion, i.e. the corresponding adenoviruses are not capable of generating functionally active E1 and/or E3 and/or E4 expression products and corresponding products, respectively.
  • these adenoviruses are only capable of generating functionally inactive E1, E3 and/or E4 expression products, whereby a functionally inactive E1, E3 and/or E4 expression product is an expression product which is either not present as an expression product at all, either at the transcription level and/or at the translation level, or is present in a form which at least does not have one of the functions attributed to it in a wildtype adenovirus.
  • a functionally inactive E1, E3 and/or E4 expression product is an expression product which is either not present as an expression product at all, either at the transcription level and/or at the translation level, or is present in a form which at least does not have one of the functions attributed to it in a wildtype adenovirus.
  • This/these function(s) inherent to the expression product in wildtype adenovirus is/are known to the ones skilled in the art and, for example, described in Russell, W. C., Journal of Virology, 81, 2573-2604, 2000.
  • each of the E1, E3 and E4 region is suitable as cloning site within the adenoviral nucleic acid, whereby the region which is not used for the cloning can either be present, or partially and/or completely deleted. In case these regions are present, in particular are completely present, it is within the present invention that these are either intact and preferably provide a translation product and/or a transcription product, and/or are not intact and preferably do not provide a translation product and/or transcription product.
  • suitable promoters are those as disclosed herein in connection with the controlling and expression, respectively, of E1A, in particularly of the modified E1A.
  • the group II adenoviruses used in accordance with the present invention are E1B deficient, particularly E1B 19 kDa deficient.
  • the term deficient as generally used herein refers to a condition, wherein the E1B does not exhibit all of the characteristics of the wildtype E1B and lacks at least one of these characteristics.
  • the adenovirus BCL2-homologue E1B19k avoids the E1A induced apoptosis by interaction with the pro-apoptotic proteins Bak and Bax. Because of this a maximum replication and/or particle formation is possible in infected cells (Ramya Sundararajan and Eileen White, Journal of Virology 2001, 75, 7506-7516). The absence of E1B 19k results in a better release of virus as, if present, it assumingly minimizes the function of the adenoviral death protein. The virus induced cytopathic effect is increased by such deletion (Ta-Chiang Liu et al., Molecular Therapy, 2004) and thus results in a more pronounced lysis of infected tumour cells.
  • TNF-alpha does not have any effect on the replication of such adenoviruses in tumour cells whereas in normal cells the treatment results in a less pronounced replication and release of infectious virus. Insofar both selectivity and specificity are increased (Ta-Chiang Liu et al., Molecular Therapy, 2004, 9, 786-803).
  • At least some embodiments of the group II adenoviruses as used in accordance with the invention disclosed herein, are as such known in the art.
  • the adenoviruses used in accordance with the invention are preferably recombinant adenoviruses, particularly also if, compared to the wildtype, a change has been made in the sense of the technical teaching provided herein. It is within the skills of those of the art to delete and mutate, respectively, the adenoviral nucleic acid sequences which are irrelevant for the invention. Such deletions may be related to, e.g. a part of the E3 and E4 coding nucleic acids as also described herein.
  • a deletion of E4 is particularly preferred provided that such deletion does not extend to the protein E4orf6, in other words the adenovirus to be used in accordance with the invention codes for E4orf6.
  • these adenoviral nucleic acids may still be packed into viral capsids and thus form infectious particles. This is also true for the use of the nucleic acids in accordance with the invention.
  • the adenoviral systems may be deficient with regard to single or several expression products.
  • this in connection with both the group I adenoviruses and the group II adenoviruses, may be caused by the mutation or deletion of the nucleic acid coding the expression product, whereby such mutation and deletion, respectively, is either a complete one or performed to the extent that no expression product is formed anymore or by the regulatory elements and elements controlling the expression such as promoters and transcription factors being missing or being active in a way different from wildtype, either at the level of the nucleic acid (lack of a promoter; cis acting elements) or at the level of the translation and transcription system (transacting elements), respectively. Particularly the latter aspect may depend on the respective cellular background.
  • adenoviruses which are as such already known, in accordance with the present invention also novel adenoviruses such as group II adenoviruses may be used for the purposes already disclosed for the other adenoviruses described herein.
  • the new adenoviruses of the invention result from the technical teaching provided herein.
  • Particularly preferred representatives are, for example, the viruses Xvir03 and Xvir03/01 which are depicted in FIGS. 16 and 17 , the design principle of which is further illustrated in examples 11 and 12.
  • a CMV promoter was cloned into the E1 region which controls the nucleic acids for E1B 55k and E4orf6 which are separated by an IRES sequence.
  • the E3 region and the E4 region can be deleted and/or be present and intact. Due to the cloning of these two genes into the virus and due to the gene products generated therefrom, respectively, a high replication efficiency results which factually corresponds to the one of wildtype viruses, whereby the selective replication in cells, preferably tumor cells, is maintained insofar as a replication occurs particularly in YB-1 nucleus-positive cells and more particularly in those cells which comprise deregulated YB-1 in the sense of the present disclosure.
  • Cells in which deregulated YB-1 is present are, in an embodiment, cells which show an increased expression of YB-1, preferably compartment independent expression of YB-1, compared to normal or non-tumour cells.
  • the introduction of E1B 55k and E4orf6 by cloning can also be made into the E4 region, whereby the E3 region can be either intact or can be deleted.
  • virus Xvir03/01 into which in a preferred embodiment therapeutic genes or transgenes have been cloned under the control of a specific promoter, in particular a tumor-specific or tissue-specific promoter.
  • a specific promoter in particular a tumor-specific or tissue-specific promoter.
  • the E3 and E4 region can be deleted and/or be resent and intact.
  • the E4 region is functionally inactive, is preferably deleted.
  • the transgenes described herein may also be cloned into the E4 region, whereby this can be done either alternatively or in addition to the cloning of the transgenes into the E3 region.
  • transgenes described herein and particularly described in the following may also be expressed in connection with or by the adenoviruses of the present invention, i.e. group I adenoviruses and their nucleic acids, respectively, or the replication systems of the invention and are thus comprised in connection with an expression cassette comprising a promoter and a nucleic acid sequence, whereby such nucleic acid sequence codes for one or several of said transgenes.
  • the E1, E3 and/or E4 regions are particularly suitable cloning sites in the adenoviral genome, however, the cloning sites are not limited thereto.
  • Transgenes may be therapeutic genes or viral genes, preferably adenoviral genes, which, preferably, are not contained in the genome of wildtype adenovirus or are not present at the site in the genome where they are present now in the particular virus.
  • the nucleic acid coding for YB-1 which may be part of the adenoviruses in an embodiment of the adenoviruses to be used in accordance with the invention, particularly group II adenoviruses, but also of the adenoviruses according to the invention, i.e. group I adenoviruses, may comprise a nucleic acid sequence which mediates the transport of YB-1 into the nucleus.
  • nucleic acids, adenoviruses and adenoviral systems according to the invention as well as the adenoviruses known in the prior art such as, for example, Onyx-15, Ad ⁇ 24, dl922-947, E1Ad/01/07, CB016, dl 520 and the adenoviruses described in patent EP 0 931 830 may be used, as adenoviruses and adenoviral systems, respectively, and the corresponding nucleic acids, in combination with these nucleic acids in accordance with the invention.
  • Suitable nucleic acid sequences mediating nuclear transport are known to the ones skilled in the art and, for example, described in Whittaker, G. R.
  • YB-1 forms a fusion protein with a signal peptide or is provided with such signal peptide and is transferred into the cellular nucleus because of the signal peptide, whereupon the replication of the adenoviruses in accordance with the invention occurs.
  • a further principle which may be used in the design of the adenoviruses to be used in accordance with the invention, particularly group II adenoviruses, but also with the adenoviruses in accordance with the present invention, i.e. the group I adenoviruses, is providing YB-1 with a transport sequence which results in the transfer or translocation of YB-1 into the cellular nucleus, preferably starting from a synthesis in the cytoplasm, and prompts viral replication there.
  • a particularly effective nucleic acid sequence mediating transport into the nucleus is the TAT sequence of HIV which is, for example, described together with other suitable nucleic acid sequences of that kind in Efthymiadis, A., Briggs, L J, Jans, D A., JBC 273, 1623-1628, 1998.
  • the adenoviruses to be used in accordance with the invention particularly group II adenoviruses, but also the adenoviruses according to the present invention, i.e. group I adenoviruses, comprise the nucleic acid sequences which code for the peptides which mediate nuclear transport.
  • YB-1 is present in its full length, particularly in a form which corresponds to wildtype YB-1. Furthermore, it is within the invention that YB-1 is used or present as a derivative, for example in a shortened or truncated form.
  • a YB-1 derivative as may be used or may be present in connection with the present invention is a YB-1 which is preferably capable of binding to the E2 late promoter and thus activates gene expression of the adenoviral E2 region.
  • Such derivatives particularly comprise the YB-1 derivatives disclosed herein. Further derivatives can be generated by deletion of single or several amino acids at the N-terminus, the C-terminus or within the amino acid sequence.
  • YB-1 fragments are used as YB-1 proteins in the sense of the present invention.
  • various YB-1 fragments are disclosed which are characterised by deletions at the C- and the N-terminus.
  • the distribution of the various YB-1 fragments has shown that both the cold shock domain (CSD) as well as the C-terminus is relevant for the cell cycle regulated transport of YB-1 into the cellular nucleus.
  • a shortened YB-1 (herein also referred to as YB-1 protein) in connection with the inventive expression of E1B55k and E4orf6 migrates better into the nucleus and thus induces a stronger CPE without necessarily binding better to the E2-late promoter compared to native YB-1, whereby it cannot be excluded that also a shortened YB-1 migrates better into the nucleus and is causing both effects, i.e. induces CPE and binds to the E2-late promoter. Finally, such shortened YB-1 fragments may also migrate better into the nucleus and bind more efficiently to the E2-late promoter without inducing a better CPE. It is also within the present invention that shortened YB-1 proteins and fragments, respectively, comprise further sequences as disclosed herein in connection with the full length YB-1, in particular cell localisation signal sequences (NLS) and the like.
  • NLS cell localisation signal sequences
  • the adenoviruses used in accordance with the invention is any respective adenoviral nucleic acid which as such or in combination with further nucleic acid sequences results in a replication event. It is possible, as explained herein, that the sequences and/or gene products necessary for replication are provided by helper viruses. To the extent it is referred to coding nucleic acid sequences and said nucleic sequences are nucleic sequences which are known, it is within the present invention that not only the identical sequence is used but also sequences derived therefrom.
  • derived sequences shall mean in particular any sequences which still result in a gene product, either a nucleic acid or a polypeptide which has a function which corresponds to a or the function of the non-derived sequence. This can be tested by routine tests known to the one skilled in the art.
  • An example for such derived nucleic acid sequences are those nucleic acid sequences which code for the same gene product, in particular for the same amino acid sequence, which, however, have a different base sequence due to the degeneracy of the genetic code.
  • the adenoviral nucleic acid is deficient for the expression of the oncogene protein, in particular is E1A protein deficient, i.e.
  • the adenoviral replication system further comprises a nucleic acid of a helper virus, whereby the nucleic acid of the helper virus comprises a nucleic acid sequence which codes for the oncogene protein, particularly the E1A protein, which has the following characteristics and confers the following characteristics to the adenovirus, respectively: It is preferably non-replicating in YB-1 nucleus-negative cells but is replicating in cells which are independent of the cell cycle in YB-1 nucleus-positive or in cells exhibiting deregulated YB-1, is transactivating at least one viral gene, in particular E1B55kDa, E4orf6, E4
  • Group I adenoviruses and/or group II adenoviruses are characterised by the various nucleic acids and gene products, respectively, disclosed herein and may otherwise comprise all those elements known to the ones skilled in the art and which are inherent to the wildtype adenoviruses (Shenk, T.: Adenoviridae: The virus and their replication. Fields Virology, vol. 3, editors Fields, B. N., Knipe, D. M., Howley, P. M. et al., Lippincott-Raven Publishers, Philadelphia, 1996, chapter 67).
  • group I and/or group II adenoviruses are capable of replicating in such cells and cellular systems, which have YB-1 in the nucleus.
  • adenoviruses used in accordance with the invention are capable of replicating and are thus capable of tumor lysis, the status of the cells with regard to the presence or absence of Rb, i.e. the retinoblastome tumor suppressor product, is irrelevant.
  • adenoviruses in accordance with the present invention, it is not necessary to take into account the p53 status of the infected cells, of the cells to be infected or of the cells to be treated as, when using the adenoviral systems disclosed herein in connection with YB-1 nucleus-positive cells, i.e. cells having YB-1 in the nucleus independent of the cell status, the p53 status as well as the Rb status does not have any impact on the replication of the adenovirus for the practising the technical teaching disclosed herein.
  • the transactivating oncogene and oncogene protein, respectively, in particular E1A, preferably of the group II adenoviruses can be either under the control of the proprietary natural adenoviral promoters and/or be controlled through a tumor-specific or tissue-specific promoter.
  • Suitable non-adenoviral promoters can be selected from the group comprising cytomegalovirus promoter, RSV (rous sarcoma virus) promoter, adenovirus-based promoter Va I and the non-viral YB-1 promoter (Makino Y. et al., Nucleic Acids Res. 1996, 15, 1873-1878).
  • telomerase promoter the alpha-fetoprotein (AFP) promoter
  • CEA carcinoembryonic antigen promoter
  • E2f promoter Teukada et al., Cancer Res., 62, 3428-3477, 2002
  • uroplakin II promoter Zhang et al., Cancer Res., 62, 3743-3750, 2002
  • PSA promoter Hallenbeck P L, Chang, Y N, Hay, C, Golightly, D., Stewart, D., Lin, J., Phipps, S., Chiang, Y L. Human Gene Therapy, 10, 1721-1733, 1999
  • tyrosinase promoter Netelbeck, D M.
  • the various promoters described above are also used in connection with the various embodiments of the adenoviruses in accordance with the invention, preferably the group I adenoviruses but also in connection with virus group ⁇ 1 and virus group ⁇ 2, particularly in case a promoter is to be used which is different from the one which controls the expression of the respective protein or expression product in wildtype adenoviruses.
  • the aforementioned promoters are thus suitable heterologous promoters in the meaning of the present invention.
  • the adenoviruses in accordance with the invention particularly the group I adenoviruses
  • E1A protein is in this and other embodiments under the control of a YB-1 controllable promoter such as for example the adenoviral E2-late promoter. This is also true in that case where the E1B protein and/or the E4 protein is/are expressed in an expression cassette.
  • a YB-1 controllable promoter such as for example the adenoviral E2-late promoter.
  • the promoter is each and independently a tumor-specific, organ-specific or tissue-specific promoter. In connection therewith it is sufficient when at least one of the promoters which control the expression of the E1B protein, the E4 protein and/or the E1A protein, is such a specific promoter.
  • adenoviruses in accordance with the invention happens only in cells of the respective tumor, organ or tissue and that, apart from that, no further tissue is damaged by the replication of the adenoviruses such as, for example, is lysed.
  • a second and more preferably all three proteins are controlled by such tumor-specific, organ-specific or tissue-specific promoters.
  • adenoviruses it is possible to lyse also those cells which do not form a tumor or which cannot develop into such tumor, but which are for other reasons such as medicinal reasons to be destroyed or to be removed from the organism, preferably a mammalian and more preferably a human organism, for example because they produce an undesired factor or produce such factor at a too high level.
  • viruses according to the invention i.e. viruses which lack a functional E1-region as present in wildtype adenoviruses, and which at the same time comprise a transporter and in particular code for such transporter which may transport or translocate YB-1 into the nucleus, are capable of replicating in cells which either contain YB-1 in the nucleus in a cell cycle independent manner, or in cells which have or comprise deregulated YB-1.
  • the viruses according to the present invention may also replicate independently of E1A13S, in particularly if the replication is mediated through YB-1.
  • the replication occurs under such conditions in particular in the afore-described cells.
  • cell which contain YB-1 in the nucleus preferably contain YB-1 in the nucleus independent of the cell cycle, are also those cells which contain YB-1 in the nucleus due to the use of the viruses in accordance with the present invention and in particular due to the infection of the cells with them.
  • protein IX is an important factor in particular for the efficacy of the viruses in accordance with the present invention, particularly when used as oncolytic viruses, and that the constructs disclosed herein provide for an expression of this factor which results in a high-level particle formation also in YB-1-mediated E1A13S-independent viral replication.
  • this group of viruses also comprises a virus replicating in a YB-1 dependent manner, whereby the virus comprises or encodes for protein IX.
  • the viruses in accordance with the present invention comprise a transporter for the transport of YB-1 to the cell nucleus.
  • the transporter is a protein, preferably a viral protein.
  • the YB-1 which is transported into the nucleus of a cell by the transporter is preferably a deregulated YB-1, in particular as defined herein.
  • YB-1 is one that is encoded, alternatively or additionally, to the deregulated YB-1 by the virus in accordance with the present invention and is expressed in the cell which is infected by the virus. Insofar the respective features as outlined in connection with the virus group ⁇ 2 herein, are also applicable to virus group ⁇ 3.
  • the cells, in which the transporter of the viruses in accordance with the present invention transports YB-1 into the nucleus, are preferably those which contain regulated YB-1.
  • a virus comprises such a transporter or codes therefor.
  • a cell which comprises YB-1 in the nucleus in a cell cycle independent manner such as for example the cervix carcinoma cell line HeLa or the osteosarcoma cell line U2OS can be used and subsequently be determined, whether due to the infection and the subsequent replication of the virus the corresponding infected cell contains YB-1 in the nucleus.
  • a cell is used as a cell in connection therewith which contains deregulated YB-1.
  • YB-1 can be detected under such experimental conditions in the nucleus using the means described herein, in particular an antibody directed against YB-1, as can be made by the one skilled in the art. If under the influence of the virus, YB-1 is detected in the cell nucleus, the tested virus comprises the transporter.
  • the E1A-region is “minus” with regard to one or both protein groups coded by the E1-region in the meaning of the afore-mentioned embodiments.
  • Said two protein groups are the group of E1A proteins, in particular the E1A13S protein, also referred to herein as E1A13S, and the E1A12S protein, also referred to herein as E1A12S, and the group of E1B proteins, in particular the E1B55k protein, also referred to herein as E1B55k, the E1B19k protein, also referred to herein as E1B19k, and the protein IX.
  • the virus is E1A13S-minus if E1A13S is under the control of a promoter which is different from the E1A promoter, preferably the adenoviral E1A-promoter and more preferably the adenoviral E1A-promoter of the wildtype;
  • the virus is E1A12S-minus if E1A12S is under the control of a promoter which is different from the E1A promoter, preferably the adenoviral E1A-promoter and more preferably the adenoviral E1A promoter of the wildtype.
  • the virus is E1B55k-minus if E1B55k is under the control of a promoter which is different from the E1B promoter, preferably the adenoviral E1A promoter and more preferably the adenoviral E1B promoter of the wildtype; the virus is E1B19k-minus if E1B 19k is under the control of a promoter which is different from the E1B promoter, preferably the adenoviral E1B promoter and more preferably the adenoviral E1B promoter of the wildtype; and it is protein IX-minus if protein IX is under the control of a promoter which is different from the E1B IX-promoter, preferably the adenoviral E1B IX-promoter and more preferably the adenoviral E1B IX-promoter of the wildtype or if it is under the control of the E1B IX-promoter, however said promoter is inactive due to the lack of in particular viral factors which
  • the term changed regulatory context thus comprises also changes which are either indirectly or at a higher integration or regulatory level active, however, in any case are different from the particularities of the wildtype, in particular the wildtype adenovirus.
  • a protein or protein function and the respective nucleic acid(s) coding therefore being “minus”, it is to be acknowledged that such protein, protein function and nucleic acid(s) coding therefore may nevertheless be contained in preferred embodiments of the viruses, but in a context which is different from the respective context in the wildtype virus.
  • Such protein, protein function and respective nucleic acid(s) is under such conditions also referred to herein as heterologous.
  • the virus is E1A13S-minus. In a further embodiment the virus is also E1A12-minus.
  • the viral E1A12S is under the control of a promoter the activity of which is controlled by YB-1, in particularly is activated by YB-1.
  • YB-1-dependent promoters are referred to herein as YB-1-dependent promoters.
  • a particularly preferred YB-1-dependent promoter is the adenoviral E2-late promoter.
  • E1A12S is specifically only expressed in such cells which contain YB-1 in a deregulated form and thus limit replication of the virus to these cells and, consequently, limit the lysis to particularly these cells which represents a significant advantage of this viral design in terms of safety.
  • the adenoviral protein IX cements the capsid structure and is important for the packaging of viral DNA into virions (Boulanger et al., Journal of Virology, 44, 783-800, 1979; Jones und Shenk, Cell, 17, 683-689, 1979).
  • the gene is located in the viral genome between positions 3581 and 4071 (Colby und Shenk T, Journal of Virology, 1981, 39, 977-980), whereby the gene for protein IX is expressed only from replicating DNA-molecules (Matsui T et al., Molecular and Cellular Biology, 1986, 6, 4149-4154).
  • Virus Xvir03-3′UTR which is described in the prior art and which performs a YB-1-dependent replication, comprises both the promoter as well as the sequence for protein IX as has been shown in analysis performed in the meantime in connection with the present invention, as the 3′UTR sequence contains the same. However, the protein is only weakly expressed in tumour cells and results in a comparatively low particle formation compared to wildtype virus.
  • the virus Xvir03-3′UTR expresses the viral proteins E1B55k and E4orf6 as mediated by the heterologous CMV promoter (company Clonetech: Plasmid pShuttle) introduced into Xvir03-3′UTR.
  • the independent promoter is preferably a promoter which is different from the E1B IX promoter.
  • the independent promoter is selected from the group comprising tissue-specific, tumour-specific, YB-1-dependent and viral promoters.
  • promoters are used for the expression of the transporter which are different from the promoter which controls the expression of the transporter in the wildtype virus.
  • the promoter is a promoter which is E1A independent, i.e. its activity is not influenced by E1A.
  • Preferred promoters are thus preferably tissue-specific promoters, tumour-specific promoters and viral promoters, in particular those described herein.
  • YB-1 dependent promoters which can be used within the present invention, in particular in connection with any aspect thereof; comprise, but are not limited to, the adenoviral E2-late promoter, the MDR-promoter [Stein et al, J. Biol. Chem., 2001, 276, 28562-28569] as well as the DNA polymerase alpha-promoter [En-Nia et al, J. Biol. Chem., 2004, Epub ahead of print].
  • Suitable non-adenoviral promoters which are useful within the present invention, can be selected from the group comprising cytomegalovirus promoter, RSV—(Rous sarcoma Virus)—Promotor, adenovirus-based promoter Va I and the non-viral YB-1-promoter (Makin Y. et al., Nucleic Acids Res. 1996, 15, 1873-1878).
  • telomerase promoter the alpha-fetoprotein (AFP)-promoter
  • CEA carcinoembryonic antigen promoter
  • L-plastin-promoter Choung, I., Schwartz, P E., Crystal, R C., Pizzorno, G, Leavitt, J., Deisseroth, A B. Cancer Gene Therapy, 6, 99:106, 1999
  • argenine-vasopressin-promoter Coulson, J M, Staley, J., Woll, P J. British J. Cancer, 80, 1935-1944, 1999
  • E2f-promoter Tsukada et al.
  • the viruses in accordance with the present invention allow for a significantly increased particle formation compared to YB-1 dependent viruses of the prior art.
  • the particle formation is increased by a factor of 2 to 50, more preferably by a factor of 10 to 50.
  • the adenovirus used in accordance with the invention is deficient with regard to E1B, in particular E1B19k deficient.
  • the term deficient refers to a condition in which EBB does not exhibit the entirety of characteristics inherent to the wildtype and at least one of these characteristics is lacking.
  • the adenovirus BCL2-homologue E1B19k prevents the E1A induced apoptosis by interaction with the pro-apoptotic proteins Bak and Bax.
  • the maximum replication and/or particle formation is possible in infected cells (Ramya Sundararajan and Eileen White, Journal of Virology 2001, 75, 7506-7516).
  • E1B19k results in a better release of the viruses as, if present, minimizes the function of the adenoviral death protein.
  • the virus induced cytopathic effect is increased by such deletion (Ta-Chiang Liu et al., Molecular Therapy, 2004) and results in a stronger lysis of the infected tumour cells.
  • the absence of E1B19k results in TNF-alpha not having any effect on the replication of such recombinant adenoviruses in tumour cells, whereas the treatment results in a reduced replication and release of infectious viruses in normal cells.
  • the selectivity and specificity are increased (Ta-Chiang Liu et al., Molecular Therapy 2004, 9, 786-803).
  • viruses used in accordance with the present invention and to be used in accordance with the present invention, in particular adenoviruses.
  • transgene comprises in an embodiment all those genes which are either not contained in the virus, in particular the adenovirus of wildtype and more preferably adenovirus Ad5 wildtype, or contained in a different regulatory context, as defined herein. It is within an embodiment of the present invention that one or several of the transgenes as described herein are coded and/or expressed by one or several helper viruses.
  • the viruses described replicate to an extent comparable to the one of wildtype viruses, preferably wildtype adenovirus, whereby such extent can already be realized with an infection number of 1 to 10 pfu/cell compared to 10 to 100 pfu/cell according to the prior art.
  • the viruses in accordance with the present invention provide for a significantly increased particle formation compared to the YB-1-dependent viruses of the prior art.
  • the particle formation is increased by a factor of 2 to 50, more preferably by a factor of 10 to 50.
  • deletions can, for example, be related to a part of the E3 and E4 coding nucleic acid as also described herein.
  • E4 it is particularly preferred if it does not extent to the protein E4orf6, which means that the adenovirus to be used in accordance with the present invention codes for E4orf6.
  • these adenoviral nucleic acids may still be packed into the viral capsid and thus form infectious particles. This is also true for the use of the nucleic acids in accordance with the present invention.
  • the adenoviral systems may be deficient with regard to single or several expression products.
  • this may, on the one hand, be based on the fact that the nucleic acid coding the expression product is completely mutated or deleted or to the extent mutated or deleted that essentially no expression product is formed any more or that the regulatory and the expression controlling elements such as promoters or transcription factors are lacking or are active in a manner different from wildtype, either at the level of the nucleic acid (lack of promoter; cis-acting elements) or at the level of the translation or transcription system (trans-acting elements).
  • the last aspect may depend on the respective cellular background.
  • viruses, viral systems, the replication systems coding or comprising the same, the nucleic acid(s) coding therefore, the vectors comprising the same are used for the manufacture of a medicament.
  • the medicament is for the treatment of the diseases described herein, in particular described in connection with the use in accordance with the present invention of the various viruses described herein.
  • adenoviruses in accordance with the present invention as medicaments and in particular in connection with systemic administration can be improved by a suitable targeting of the adenoviruses.
  • the infection of tumor cells by adenovirus depends to a certain extent, among others, on the presence of the coxackievirus-adenovirus receptor CAR and particular integrins. If these are strongly expressed in cells, in particular tumor cells, an infection is already possible at very low titers (pfu/cell).
  • viruses described herein comprise one or several transgenes as described herein.
  • transgenes are either important or helpful with regard to the mode of action, more precisely mode of replication of the viruses, or with regard to their use as medicaments in which case the transgenes are, in some embodiments, therapeutic genes.
  • the various transgenes including E1B55kD, E4orf6, ADP and the like, in particular if they are viral genes, may in principle be cloned from any respective virus, preferably adenovirus and more preferably adenovirus Ad5.
  • a variety of plasmids are additionally described in the prior art which contain the respective genes and from which these may accordingly be taken and introduced into both the adenoviruses in accordance with the present invention as well as the viruses to be used in accordance with the present invention.
  • An example for a plasmid expressing E1B55kD is, for example, described by Dobbelstein, M. et al., EMBO Journal, 16, 4276-4284, 1997.
  • the coding region of the E1B55K gene can, for example, can be excised together with the 3′ non-coding region (the 3′UTR region lies preferably at about base position 3507-4107 of the adenovirus wildtype genome) of this gene by means of Bam HI from the plasmid pDCRE1B.
  • the respective fragment comprising the E1B55kD gene as well as the 3′ non-coding region corresponds to nucleotides 2019 to 4107 of the adenovirus type 5.
  • the E1B55kD gene is excised from the plasmid by means of the restriction enzymes Bam HI and BfrI and XbaI, respectively, and subsequently cloned into the adenovirus.
  • analogues thereof and in particular analogues of the 3′ UTR region may be used within the present invention.
  • An analogue of the 3′ UTR region is any sequence which has the same effect as the 3′ UTR region, particularly the same effect with regard to the expression of a gene, preferably the E1B55kD gene.
  • Such analogues can be determined by routine experiments performed by the ones skilled in the art, e.g.
  • 3′ UTR region thus comprises also each and any analogue thereof.
  • viruses where therapeutic genes or transgenes are cloned in a preferred embodiment preferably under the control of a specific promoter, in particular a tumor-specific or tissue-specific promoter are further developments of the viruses in accordance with the present invention. It is also within such viruses that also the E4 region is functionally inactive and is preferably deleted.
  • the transgenes described herein can also be cloned into the E4 region, whereby this may be performed alternatively or additionally to the cloning of the transgenes into the E3 region and the E3 region may remain partially or completely intact, respectively.
  • Transgenes as used herein may be therapeutic genes or viral genes, preferably adenoviral genes, which preferably are not present in the genome of wildtype adenoviruses and which are not present, respectively, at a site of the genome at which they are located in the particular virus now.
  • Therapeutic genes can be prodrug genes, genes for cytokines, apoptosis inducing genes, tumor suppressor genes, genes for metalloproteinase inhibitors and/or angiogenesis inhibitors, and tyrosine kinase inhibitors. Additionally, siRNA, aptamers, antisense molecules and ribozymes may be expressed which are preferably directed against cancer-relevant target molecules.
  • the individual or the several target molecules are selected from the group comprising the resistance-relevant factors, anti-apoptosis factors, oncogenes, angiogenesis factors, DNA synthesis enzymes, DNA repair enzymes, growth factors and their receptors, transcription factors, metalloproteinases, particularly matrix metalloproteinases, and plasminogen activator of the urokinase type. Preferred embodiments thereof are already disclosed herein.
  • the resistance-relevant factors are preferably selected from the group comprising P-glycoprotein, MRP and GST and also comprise the nucleic acids coding therefor.
  • Possible prodrug genes are, for example, cytosine deaminase, thymidine kinase, carboxypeptidase, uracil phosphoribosyl transferase; or purine nucleoside phosphorylase (PNP); Kim et al, Trends in Molecular Medicine, volume 8, no. 4 (suppl), 2002; Wybranietz W. A. et al., Gene Therapy, 8, 1654-1664, 2001; Niculescu-Duvaz et al., Curr. Opin. Mol.
  • PNP purine nucleoside phosphorylase
  • Possible cytokines are, for example, GM-CSF, TNF-alpha, 1′-12, 17-2, 17-6, CSF or interferon-gamma; Gene Therapy, Advances in Pharmacology, volume 40, editor: J. Thomas August, Academic Press; Zhang and Degroot, Endocrinology, 144, 1393-1398, 2003; Descamps et al., J. Mol. Med., 74, 183-189, 1996; Majumdar et al., Cancer Gene Therapy, 7, 1086-1099, 2000.
  • the anti-apoptosis factors are selected from the group comprising BCL2 and comprise also the nucleic acids coding therefor.
  • the oncogenes are selected from the group comprising Ras, particularly mutated Ras, Rb and Myc, and comprises also the nucleic acids coding therefor.
  • the angiogenesis factors are selected from the group comprising VEGF and HMG proteins, and also comprise the nucleic acids coding therefor.
  • the DNA synthesis enzymes are selected from the group comprising telomerase, and also comprise the nucleic acids coding therefor.
  • the DNA repair enzymes are selected from the group comprising Ku-80, and also comprise the nucleic acids coding therefor.
  • the growth factors are selected from the group comprising PDGF, EGF and M-CSF, and also comprise the nucleic acids coding therefor.
  • the receptors are in particular those of growth factors, whereby preferably the growth factors are selected from the group comprising PDGF, EGF and M-CSF, and also comprise the nucleic acids coding therefor.
  • the transcription factor is selected from the group comprising YB-1, and also comprises the nucleic acid coding therefor.
  • the metalloproteinases are in particular matrix metalloproteinases.
  • the matrix metalloproteinases are selected from the group comprising MMP-1 and MMP-2, and also comprise the nucleic acids coding therefor.
  • the plasminogen activators of the urokinase type are selected from the group comprising uPa-R, and also comprise the nucleic acids coding therefor.
  • Possible apoptosis-inducing genes are, for example, Decorin: Tralhao et al., FASEB J, 17, 464-466, 2003; retinoblastoma 94: Zhang et al., Cancer Res., 63, 760-765, 2003; Bax and Bad: Zhang et al., Hum. Gene Ther., 20, 2051-2064, 2002; apoptin: Noteborn and Pietersen, Adv. Exp. Med.
  • Possible tumor suppressor genes are, for example, E1A, p53, p16, p21, p27 or MDA-7: Opalka et al., Cell Tissues Organs, 172, 126-132, 2002, Ti et al., Cancer Res., 59, 3333-3339, 1999, Su et al., Oncogene, 22, 1164-1180, 2003.
  • angiogenesis inhibitors are, for example, endostatin or angiostatin: Hajitou et al., FASEB J., 16, 1802-1804, 2002, and antibodies against VEGF: Ferrara, N., Semin Oncol 2002 December; 29 (6 suppl 16): 10-4.
  • Possible metalloproteinase inhibitors as may be used in preferred embodiments are, for example, Timp-3 [Ahonen et al., Mol Therapy, 5, 705-715, 2002]; PAI-1 [Soff et al., J. Clin. Invest., 96, 2593-2600, 1995]; Timp-1 [Brandt K. Curr. Gene Therapy, 2, 255-271, 2002].
  • transgenes in the sense of the present invention which may be expressed by both group I adenoviruses and group H adenoviruses in accordance with the present invention are also tyrosine kinase inhibitors.
  • Exemplary tyrosine kinases are EGFR (epidermal growth factor receptor) [Onkologie, Entstehung and Progression maligner Tumoren; author: Christoph Wagner, Georg Thieme Verlag, Stuttgart, 1999].
  • a preferred tyrosine kinase inhibitor is herceptin [Zhang H et al., Cancer Biol Ther. 2003, July-August; 2 (4 suppl 1): S122-6].
  • SiRNA short interfering RNA
  • siRNA specifically induces or mediates the degradation of mRNA.
  • siRNA is a biological strategy for cells in order to inhibit distinct alleles during development and to protect themselves against viruses.
  • siRNA mediated RNA interference is used as a method for the specific suppression or complete elimination of the expression of a protein by introducing a gene specific double-stranded RNA.
  • a siRNA comprising 19 to 23 nucleotides is insofar particularly suitable as it does not result in the activation of a non-specific defense reaction such as an interleukin response.
  • RNA interference was suitable to mediate RNA interference in mammalian cells and is highly efficient compared to other technologies such as ribozymes and antisense molecules (Elbashir, S. Harborth S. Lendeckel W. Yalvcin, A. Weber K, Tuschl T: Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature 2001, 411: 494-498). As little as a few siRNA molecules are sufficient so as to suppress expression of the target gene.
  • vectors are used in the prior art which allow for an endogenous siRNA expression.
  • oligonucleotides having a length of 64 nucleotides are introduced into the vector which comprise the 19 nucleotide long target sequence both in the sense and in the antisense orientation, separated by, for example, a 9 nucleotide spacer sequence.
  • the resulting transcript folds into a hairpin structure with a stem structure (stem) of; for example, 19 base pairs.
  • the loop is rapidly degraded in the cell so that a functional siRNA molecule is generated (Brummellcamp et al., Science, 296, 550-553, 2002).
  • the medicament further comprises at least one pharmaceutically active compound or pharmaceutically active agent, whereby the terms compound and agent are used in an interchangeable manner if not explicitly indicated to the contrary.
  • the pharmaceutically active compound is selected from the group comprising cytokines, metalloproteinase inhibitors, angiogenesis inhibitors, cytostatics such as Irinotecan and CPT-11 against colorectal carcinoma and Daunorubicin against leukemia, cell cycle inhibitors such as CYC202 which inhibits CDK2/CyclinE kinase activity and can be used against colorectal tumors (McClue S J, Int. J. Cancer 2002, 102, 463-468) and BAY 43-9006 which inhibits Raf-1 and is, for example, effective against mamma carcinoma (Wilhelm S M et al., Cancer Res.
  • proteosome inhibitors such as PS-341 which inhibits the 26S proteasome activity and is used against squamous-cell carcinoma (Fribley A et al., Mol Cell Biol 2004 November; 24(22): 9695-704), recombinant antibodies such as against the EGF receptor (Herceptin for breast carcinoma and prostate tumor; H. G. van der Poel, European Urology 2004, 1-17; Erbitux against head and neck tumors; Bauman M et al., Radiother. Oncol., 2004, 72, 257-266), and inhibitors of the signal transduction cascade such as STI 571 which represses, among others, c-kit and can be used against gastrointestinal tumors (H. G.
  • van der Poel European Urology 2004, 45, 1-17
  • ABT-627 an endothelin inhibitor which may be used, among others, against prostate tumors
  • SU5416 which inhibits phosphorylation of the VEGF tyrosine kinase receptor and which may be used against glioblastoma and prostate cancer
  • ZD1839 which inhibits EGFR tyrosine activity and may be used, among others, against prostate tumors
  • rapamycin derivatives such as CCI-779 and RAD001 which inhibit mTOR and can be used against prostate tumors.
  • the various adenoviruses described herein and the adenoviruses to be used in accordance with the present invention, respectively can, in principle, be used with each and any of the aforementioned compounds for each and any of the indication described in connection therewith.
  • the indication is the one which is described for any of the previously mentioned pharmaceutically active compounds or agents.
  • the present inventor has furthermore surprisingly found that the efficacy of the viruses described herein and in particular the viruses used in accordance with the present invention can be increased by using in combination at least two compound whereby each of the at least two compounds is individually and independently selected from the group comprising cytostatics.
  • cytostatics are in particular chemical or biological compounds which; during or after the administration to a cell or an organism containing a or such cell, result in the cell no longer growing and/or no longer dividing or slowing down cell division and/or cell growth.
  • Cytostatics also comprise compounds or agents which turn into a cytostatic in the aforedescribed sense only in the cell or in an organism containing such cell. Insofar, the term cytostatics also comprises pre-cytostatics.
  • Cytostatics are grouped according to their mode of action. The following groups are distinguished which, in principle, can all be used within the present invention:
  • At least one and preferably two agents are selected from the aforementioned group. It is, however, also within the invention that in particular also three, four or five different agents are selected. The following comments are made for the embodiment of the present invention where only one and preferably two agents are used together with the virus.
  • the agents differ from each other such that they address different target molecules or are described in literature as targeting different molecules. It is within the present invention that the agent also comprises two or more different agents which bind to the same target molecule. It is also within the present invention that one such agent binds to a first site of the target molecule, whereas the second such agent binds to a second site of the target molecule.
  • At least two of the agents are active using different modes of action. Active means in a preferred embodiment that the cell growth and/or cell division inhibiting or retarding effect of the chemical compound is mediated through a different mode of action.
  • the term active means that the replication efficiency of a virus, in particular the virus in accordance with the present invention, of the viruses described herein and of the viruses to be used in accordance with the present invention, is increased compared to a scenario where one and/or both of the agents are not used.
  • the efficiency of viral replication preferably the number of viruses required for cell lysis is used, preferably expressed as pfu/cell.
  • At least one of the at least two agents is one which increases the infectability of the cell in which the replication of the virus is to occur, preferably is to occur in a selective manner, preferably with the virus described herein and/or the virus to be used in accordance with the present invention.
  • This can, e.g., be performed by increasing the uptake of the virus by the cell.
  • the uptake of the virus, in particular of adenovirus is, for example, mediated by the coxsackievirus-adenovirus receptor (CAR) (Mizuguchi and Hayakawa, GENE 285, 69-77, 2002).
  • An increased expression of CAR is, for example, caused by trichostatin A (Vigushin et al., Clinical Cancer Research, 7, 971-976, 2001).
  • one of the at least two agents is one which increases the availability of a component within the cell, whereby the component is one which increases the replication of the virus, preferably the virus described herein and/or the virus to be used in accordance with the present invention.
  • one of the at least two agents is one which mediates the transport of YB-1 into the nucleus.
  • Such an agent can be selected from the group comprising topoisomerase inhibitors, alkylating agents, antimetabolites and mitosis inhibitors.
  • Preferred topoisomerase inhibitors are camptothecin, irinotecan, etoposide and their respective analogues.
  • Preferred mitosis inhibitors are daunorubicin, doxorubicin, paclitaxel and docetaxel.
  • Preferred alkylating agents are cis platin and their analogues.
  • Preferred antimetabolites are fluorouracil and methotrexat.
  • one of the at least two agents is one which increases the infectability of the cell, in particular the expression of CAR, and the second of the at least agents is one which increases the transport of YB-1 into the nucleus, whereby preferably as chemical compound a compound is used which exhibits the respective required characteristic as preferably described above.
  • the one of the at least two agents is a histone deacylase inhibitor.
  • a preferred histone deacylase inhibitor is one which is selected from the group comprising trichostatin A, FR901228, MS-27-275, NVP-LAQ824 and PXD101.
  • Trichostatin A is, for example, described in Vigushin et al., Clinical Cancer Research, 7, 971-976, 2001;
  • FR901228 is, for example, described in Kitazono et al., Cancer Res., 61, 6328-6330, 2001; MS-27-275 is described in Jaboin et al., Cancer Res., 62, 6108-6115, 2002;
  • PXD101 is described in Plumb et al., Mol. Cancer. Ther., 8, 721-728, 2003; NVP-LAQ824 is described in Atadja et al., Cancer Res., 64, 689-695, 2004.
  • At least one agent is selected from the group comprising trichostatin A (against glioblastoma, Kim J H et al., Int. J. Radiation Oncology Biol. Phys. 2004, 59, 1174-1180), FR 901228 (against pancreas tumors, Sato N et al., Int. J. Oncol. 2004, 24, 679-685; MS-27-275 (against prostate tumors; Camphausen K et al., Clinical Canver Research 2004, 10, 6066-6071), NVP-LAQ824 (against leukemiae; Ninimanapalli R et al., Cancer Res.
  • trichostatin A as wellst glioblastoma, Kim J H et al., Int. J. Radiation Oncology Biol. Phys. 2004, 59, 1174-1180
  • FR 901228 against pancreas tumors, Sato N et al.
  • histone deacetylase inhibitors are, among others, described in Lindemann R K et al., Cell Cycle 2004, 3, 77-86. It is within the present invention that the various adenoviruses described herein and the adenoviruses to be used in accordance with the present invention, may be used with the aforementioned compounds, in principle, for each and any of the indications described herein in connection therewith. In a particularly preferred embodiment the indication is one as has been described for each and any of the aforementioned pharmaceutically active compounds.
  • the one of the at least two agents is a topoisomerase inhibitor, preferably a topoisomerase I inhibitor.
  • a preferred topoisomerase inhibitor is one which is selected from the group comprising camptothecin, irinotecan, topotecan, SN-38, 9-aminocamptothecin, 9-nitrocamptothecin, DX-895If and daunorubicin.
  • Irinotecan and SN-38 are, for example, described in Gilbert et al., Clinical Cancer Res., 9, 2940-2949, 2003; DX-8951F is described in van Hattum et al., British Journal of Cancer, 87, 665-672, 2002; camptothecin is described in Avemann et al., Mol. Cell. Biol., 8, 3026-3034, 1988; 9-aminocamptothecin, 9-nitrocamptothecin are described in Rajendra et al., Cancer Res., 63, 3228-3233, 2003; daunorubicin is described in M. Binaschi et al., Mol. Pharmacol., 51, 1053-1059.
  • the topoisomerase inhibitor is selected from the group comprising camptothecin, irinotecan, topotecan, DX-8951f, SN-38, 9-aminocamptothecin, 9-nitrocamptothecin, etoposid and daunorubicin.
  • camptothecin irinotecan, topotecan
  • DX-8951f DX-8951f
  • SN-38 9-aminocamptothecin
  • 9-nitrocamptothecin 9-nitrocamptothecin
  • etoposid daunorubicin.
  • the fields of application are, among others, described by Recchia F et al., British J. Cancer 2004, 91, 1442-1446; Cantore M et al., Oncology 2004, 67, 93-97; Maurel J. et al., Gynecol.
  • the various adenoviruses described herein and the adenoviruses to be used in accordance with the present invention, respectively, may in principle be used with the aforementioned compounds for each and any of the indications described herein in connection therewith.
  • the indication is such as described for each of the aforementioned pharmaceutically active compounds.
  • At least one agent is selected from the group comprising trichostatin A, FR 901228 (against pancreas tumors, Sato N et al., Int. J. Oncol. 2004, 24, 679-685; MS-27-275 (against prostate tumors; Camphausen K et al., Clinical Canver Research 2004, 10, 6066-6071), NVP-LAQ824 (against leukemiae; Nimmanapalli R et al, Cancer Res. 2003, 63, 5126-5135; PXD101 (against ovary tumors, Plumb J A et al, Mol. Cancer. Ther.
  • the various adenoviruses described herein and the adenoviruses to be used in accordance with the present invention may be used with the aforementioned compounds, in principle, for each and any of the indications described herein in connection therewith.
  • the indication is one as has been described for each and any of the aforementioned pharmaceutically active compounds.
  • the topoisomerase inhibitor is selected from the group comprising camptothecin, irinotecan, topotecan, DX-895If, SN-38, 9-aminocamptothecin, 9-nitrocamptothecin, daunorubicin and etoposid. These may be used against various tumors, for example, colorectal tumors, pancreas tumors, ovary carcinomas, lung tumors and prostate carcinomas. The fields of application are, among others, described by Recchia F et al., British J. Cancer 2004, 91, 1442-1446; Cantore M et al., Oncology 2004, 67, 93-97; Maurel J.
  • the various adenoviruses described herein and the adenoviruses to be used in accordance with the present invention, respectively, may in principle be used with the aforementioned compounds for each and any of the indications described herein in connection therewith.
  • the indication is such as described for each of the aforementioned pharmaceutically active compounds.
  • the one of the at least two agents is a histone deacylase inhibitor and the other one of the at least two agents is a topoisomerase inhibitor.
  • the further pharmaceutically active compound is selected from the group comprising cytokines, metalloproteinase inhibitors, angiogenesis inhibitors, cytostatics such as irinotecan and CPT-11 against colorectal carcinoma and daunorubicin against leukemia, cell cycle inhibitors such as CYC202 which inhibits CDK2/CyclinE kinase activity and can be used against colorectal tumors (McClue S J, Int. J. Cancer 2002, 102, 463-468) and BAY 43-9006 which inhibits Raf-1 and is effective against mamma carcinoma (Wilhelm S M et al., Cancer Res.
  • cytokines metalloproteinase inhibitors
  • angiogenesis inhibitors cytostatics
  • cytostatics such as irinotecan and CPT-11 against colorectal carcinoma and daunorubicin against leukemia
  • cell cycle inhibitors such as CYC202 which inhibits CDK2/CyclinE kinas
  • proteosome inhibitors such as PS-341 which inhibits the 26S proteasome activity and is used against brain tumors
  • recombinant antibodies such as against the EGF receptor (Herceptin for breast carcinoma and prostate tumor; H. G. van der Poel, European Urology 2004, 1-17; Erbitux against head and neck tumors; Bauman M et al., Radiother. Oncol., 2004, 72, 257-266)
  • inhibitors of the signal transduction cascade such as STI 571 which represses, among others, c-kit and can be used against gastrointestinal tumors (H. G.
  • van der Poel European Urology 2004, 45, 1-17
  • ABT-627 an endothelin inhibitor which may be used, among others, against prostate tumors
  • SU5416 which inhibits phosphorylation of the VEGF tyrosine kinase receptor and which may be used against head/neck tumors
  • ZD1839 which inhibits EGFR tyrosine activity and may be used, among others, against prostate tumors
  • rapamycin derivatives such as CCI-779 and RAD001 which inhibit mTOR and can be used against prostate tumors
  • H. G. van der Poel European Urology 2004, 45, 1-17
  • the various adenoviruses described herein and the adenoviruses to be used in accordance with the present invention, respectively can, in principle, be used with each and any of the aforementioned compounds for each and any of the indications described in connection therewith.
  • the indication is the one which is described for any of the previously mentioned pharmaceutically active compounds.
  • the means according to the present invention and/or the means prepared in accordance with the present invention contains the virus separate from one or several of the at least one and preferably at least two agents which are combined or administered together with the virus in accordance with the present invention.
  • the virus is separate from any agent which is combined with the virus.
  • the separation is a spatial separation.
  • the spatial separation can be such that the virus is present in a different package than the agent.
  • the package is a single dose unit, i.e. the virus and the agent(s) are packed as single dosages.
  • the single dose units may in turn be combined to form a package.
  • the single dosages of the virus are combined with one or several single dosages of one or several of the agents or packed therewith.
  • the virus will be present in a lyophilized form or in a suitable liquid phase.
  • the agents will be present in solid form, e.g. as tablets or capsules, however, are not limited thereto. Alternatively, also the agents can be present in liquid form.
  • the virus is systemically or locally administered. It is also within the present invention that the agents combined with the virus are systemically or locally administered individually and independently from each other or together. Other modes of administration are known to the ones skilled in the art.
  • the virus and the agents combined with it are administered in a chronologically separate manner or at the same time.
  • the agent is administered prior to the administration of the virus. How long the agent is administered prior to the virus depends on the kind of the agent used and is obvious for the one skilled in the art from the mode of action of the agent used. Also the administration of the at least two agents can occur at the same or at different points in time. In connection with a chronologically different administration the points of time again result from the modes of action underlying the agents and can, based thereon, be determined by the ones skilled in the art.
  • kits comprise the virus and/or the one or the several agents in a form ready for use and preferably instructions for use.
  • nucleic acids as disclosed herein and the nucleic acids used in accordance with the present invention, and the replication systems in accordance with the present invention and the nucleic acids coding therefor, and the replication systems used in accordance with the present invention and the nucleic acids coding therefor used in accordance with the present invention.
  • the medicament in connection with which or for the manufacture of which the adenoviruses disclosed herein are used in accordance with the present invention is intended to be applied, usually, in a systemic manner, although it is also within the present invention to apply or deliver it locally.
  • the application is intended to infect particularly those cells with adenoviruses and it is intended that adenoviral replication particularly occurs therein, which are involved, preferably in a causal manner, in the formation of a condition, typically a disease, for the diagnosis and/or prevention and/or treatment of which the inventive medicament is used.
  • Such a medicament is preferably for the treatment of tumor diseases.
  • Those tumor diseases are particularly preferred where YB-1 is, due to the mechanism underlying the tumor disease, in particular due to the underlying pathological mechanism, already located in the nucleus, or where the presence of YB-1 in the cellular nucleus is caused by exogenous measures whereby such exogenous measures are suitable to transfer YB-1 into the cellular nucleus or to induce or to express it there.
  • the term tumor or tumor disease shall comprise herein both malignant as well as benign tumors, and respective diseases.
  • the medicament comprises at least one further pharmaceutically active compound. The nature and the amount of such further pharmaceutically active compound or agent will depend on the kind of indication for which the medicament is used.
  • cytostatics such as cis-platin and taxole, daunoblastin, daunorubicin, adriamycin and/or mitoxantrone or others of the cytostatics or groups of cytostatics described herein, are used.
  • the medicament in accordance with the invention can be present in various formulations, preferably in a liquid form.
  • the medicament will contain adjuvants such as stabilisers, buffers, preservatives and the like which are known to the one skilled in the art of formulations.
  • the medicament in connection with which or in connection with the manufacture of which the adenoviruses described herein are used in accordance with the present invention is envisaged to be typically administered in a systemic manner, although it is also within the present invention that it is applied locally or delivered locally.
  • the application intends to infect those cells with the adenovirus and to cause adenoviral replication therein, which are involved, preferably in a causal manner, in the formation of a condition, typically a disease for the diagnosis and/or prevention and/or treatment of which the medicament according to the present invention is used.
  • Such a medicament is preferably for the treatment of tumor diseases.
  • Those tumor diseases are particularly preferred where YB-1 is, due to the mechanism underlying the tumor disease, in particular due to the underlying pathological mechanism, already located in the nucleus, or where the presence of YB-1 in the cellular nucleus is caused by exogenous measures whereby such exogenous measures are suitable to transfer YB-1 into the cellular nucleus or to induce or to express it there.
  • the term tumor or tumor disease shall comprise herein both malignant as well as benign tumors, and respective diseases.
  • the medicament comprises at least one further pharmaceutically active compound. The nature and the amount of such further pharmaceutically active compound will depend on the kind of indication for which the medicament is used.
  • cytostatics such as cis-platin and taxole, daunoblastin, daunorubicin, adriamycin and/or mitoxantrone or others of the cytostatics or groups of cytostatics described herein.
  • the medicament in accordance with the invention can be present in various formulations, preferably in a liquid form.
  • the medicament will contain adjuvants such as stabilisers, buffers, preservatives and the like which are known to the one skilled in the art of formulations.
  • the present inventor has surprisingly found that the viruses in accordance with the present invention can be used with a very high rate of success with those tumors where YB-1 is contained in the nucleus independent of the cell cycle and such tumors which contain deregulated YB-1.
  • YB-1 is present in the cytoplasma and in particular also in the perinuclear plasma.
  • YB-1 is present in the nucleus of both normal as well as tumor cells during the S-phase of the cell cycle. This, however, is not sufficient so as to provide for a viral oncolysis when using such modified adenoviruses.
  • the comparatively low efficiency of such attenuated adenoviruses as reported in the prior art, is ultimately based on the wrong application thereof.
  • adenovirus systems could be used, in particular also with an increased efficacy under conditions where the molecularbiological prerequisites for viral oncolysis using the attenuated or modified adenoviruses as described herein, are met.
  • Such prerequisites are given in tumor diseases the cells of which have YB-1 in the nucleus independent of the cell cycle or contain deregulated YB-1.
  • This form of nuclear localisation may be caused by the nature of the tumor itself, or be caused by the agents in accordance with the present invention as described herein or by applying the measures described herein.
  • the present invention thus defines a new group of tumours and tumour diseases, respectively and thus also of patients which may be treated using the virus in accordance with the present invention and in particular also with the attenuated or modified adenoviruses already described in the prior art.
  • a further group of patients which may be treated using the viruses in accordance with the present invention are those patients where it is ensured that YB-1 migrate into the nucleus or is induced there or is transported there upon applying or realizing certain conditions, including the use of the viruses in accordance with the present invention.
  • the use of the adenoviruses in accordance with the present invention in connection with this group of patients is insofar based on the finding that the induction of viral application is based on the nuclear localisation of YB-1 with subsequent binding of YB-1 to the E2-late-promoter. This applies also to those cells which are YB-1 nucleus-positive and/or cells where YB-1 is present in a deregulated manner in the meaning of the present application.
  • the adenoviruses in accordance with the present invention can be used in accordance with the present invention for the treatment of diseases and groups of patients, which comprise cells having these characteristics, particularly if these cells are involved in the forming of the respective disease to be treated.
  • a further group of patients which can be treated by using the viruses in accordance with the present invention, in particular adenoviruses are those which are YB-1 nucleus-positive as a result of the subsequently described treatments and/or patients which have undergone one of the measures described herein, preferably in the sense of a treatment, or have experienced the administration of the viruses in accordance with the present invention or experience them together with the administration of the virus in accordance with the present invention.
  • YB-1 nucleus-positive patients are patients which have YB-1 in the nucleus independent of the cell cycle and in particular in a number of tumour forming cells.
  • measures comprise the administration of such cytostatics as they are generally described herein and/or as they are used in connection with a tumour therapy.
  • this group of measures comprises radiation, in particular radiation as used in connection with a tumour therapy. Radiation means in particular the radiation with energy-rich radiation, preferably radioactive radiation, preferably as used in connection with tumour therapy.
  • a further measure is hyperthermia and the application of hyperthermia, preferably hyperthermia as used in connection with tumour therapy. In a particularly preferred embodiment hyperthermia is applied locally.
  • hormone treatment in particular hormone treatment as used in connection with tumour treatment.
  • anti-estrogens and/or anti-androgens are used.
  • anti-estrogens such as Tamoxifen
  • anti-androgens as, for example, Flutamide and Cyproteronacetate, are used in the therapy of prostate cancer.
  • some of the tumor forming cells which either inherently contain YB-1 in the nucleus or do so or after induction and active introduction into the nucleus or which comprise deregulated YB-1 in the meaning of the present disclosure.
  • Preferably about 5% or any percentage higher than that, i.e. 6%, 7%, 8% etc., of the tumor forming cells are such YB-1 nucleus-positive cells or cells in which deregulated YB-1 is present.
  • the percentage of tumor cells which comprise deregulated YB-1 or which show nuclear localisation of YB-1 independent of the cell cycle may be about 30 to 50% [Kohno K.
  • Such tumors may preferably be treated using the adenoviruses in accordance with the present invention.
  • Nuclear localisation of YB-1 may be induced by outside stress and locally applied stress, respectively. This induction may occur through irradiation, particularly UV-irradiation, application of cytostatics as, among others, also disclosed herein, and hyperthermia.
  • the medicament of the invention would thus also be administered to patients and groups of patients or would be designed for them, where by appropriate pre-treatment or concomitant treatment a transport of YB-1, particularly in the respective tumor cells, is caused and deregulated YB-1 is generated in the cell, respectively.
  • a resistance preferably a multiple resistance or poly-resistance.
  • Resistance preferably refers to a resistance to the cytostatics described herein and/or radiation.
  • This multiple resistance preferably goes along with the expression, preferably an overexpression of the membrane-bound transport protein P-glycoprotein which is a marker for the determination of respective cells and thus also of tumors exhibiting the same and the corresponding patient groups.
  • resistance as used herein comprises both the resistance which is also referred to as classical resistance and is mediated by the P-glycoprotein, as well as the resistance which is also referred to as atypical resistance and which is mediated by MRP or other, non-P-glycoprotein mediated resistances.
  • Further resistances as referred to herein and which are characteristic for the tumors and patients, respectively, to be treated, are those which hare mediated by the following genes, however, are not limited thereto: MDR, MRP, topoisomerase, BCL2, glutathione-S-transferase (GST), protein kinase C (PKC).
  • apoptosis relevant genes plays an important role in the formation of resistance so that also the following factors are relevant insofar, namely Fas, the BCL2-family, HSP70 and EGFR [Kim et al., Cancer Chemther. Pharmacol. 2002, 50, 343-352].
  • a further marker which correlates with the expression of YB-1 is Topoisomerase II ⁇ .
  • Topoisomerase II ⁇ can be used in a screening method to determine whether a patient may be treated with the adenoviruses in accordance with the present invention with an expectation of success.
  • MDR International: multiple drug resistance
  • p73 Kamiya, M., Nakazatp, Y., J Neurooncology 59, 143-149 (2002); Stiewe et al., J. Biol. Chem., 278, 14230-14236, 2003).
  • tumor refers in general also to any tumor or cancer disease which either inherently contains YB-1 in the cellular nucleus, preferably independent of the cell cycle, or does so by applying exogenous measures, as disclosed herein, and/or which contains deregulated YB-1.
  • viruses described herein can be used, in principle, for the treatment of tumours.
  • tumours which can in particular be treated by the viruses described herein are preferably those tumours which are selected from the group comprising tumours of the nervous system, ocular tumours, tumours of the skin, tumours of the soft tissue, gastrointestinal tumours, tumours of the respiratory system, tumour of the skeleton, tumours of the endocrine system, tumours of the female genital system, tumours of a mammary gland, tumours of the male genital system, tumours of the urinary outflow system, tumours of the haematopoietic system including mixed and embryonic tumours. It is within the present invention that these tumours are in particular resistant tumours as in particular defined herein.
  • the group of tumors of the nervous system preferably comprises:
  • the group of the ocular tumors preferably comprises:
  • the group of skin tumors preferably comprises:
  • the group of tumors of the soft-tissues preferably comprises:
  • the group of gastrointestinal tumors preferably comprises:
  • the group of the tumors of the respiratory system preferably comprises:
  • the group of the skeleton tumors preferably comprises:
  • the group of the tumors of the endocrine system preferably comprises:
  • the group of the tumors of the female sexual system tumors preferably comprises:
  • the group of tumors of the mammary glands preferably comprises:
  • the group of the tumors of the male sexual system preferably comprises:
  • the group of tumors of the urinary outflow system preferably comprises:
  • the group of tumors of the haematopoietic system preferably comprises:
  • the group of the mixed and embryonal tumors preferably comprises:
  • these tumors are selected from the group comprising breast cancer, ovary carcinoma, prostate carcinoma, osteosarcoma, glioblastoma, melanoma, small-cell lung carcinoma and colorectal carcinoma.
  • Further tumors are those which are resistant as described herein, preferably those which are multiple resistant, particularly also those tumors of the group described above.
  • Especially preferred tumors are also those selected from the group comprising breast tumors, bone tumors, stomach tumors, intestinal tumors, gallbladder tumors, pancreatic tumors, liver tumors, kidney tumors, brain tumors, ovary tumors, tumors of the skin and of cutaneous appendages, head/neck tumors, uterus tumors, synovial tumors, larynx tumors, oesophageal tumors, tongue tumors and prostate tumors. It is preferred that the tumors are those which are disclosed herein regarding their manifestations.
  • Further tumours which may be treated in accordance with the present invention are selected from the group comprising primary tumours, secondary tumours, tertiary tumours and metastasizing tumours. It is preferred if the tumours comprise at least one of the following features, namely that they have YB-1 in the nucleus independent of the cell cycle, regardless what the reason therefore is, and/or that they comprise deregulated YB-1.
  • tumours which may be treated using the viruses in accordance with the present invention, are all of the afore-mentioned tumours and tumours, respectively, which are described as being treatable using the viruses according to the present invention, provided that they have one or several of the resistances disclosed herein.
  • tumours can be treated using the viruses in accordance with the present invention, which do neither contain YB-1 in the nucleus, preferably independent of the cell cycle, nor deregulated YB-1. This is realized in particular if the viruses themselves code for YB-1.
  • the expression of the viruses is put under the control of a preferably highly regulated promoter in a preferred embodiment.
  • a promoter could be any of promoters which can be activated in a specific manner so that the viruses can only replicate in the intended cells.
  • Particularly preferred promoters are in particular tumour-specific promoters and tissue-specific promoters which are known to the ones skilled in the art.
  • YB-1 belongs to the group of highly conserved factors which bind to an inverted CAAT sequence, the so-called Y-box. They may be active in a regulatory manner both at the level of transcription as well as translation (Wolffe, A. P. Trends in Cell Biology 8, 318-323, 1998).
  • the nucleic acid coding for YB-1 which, in an embodiment of the viruses to be used in accordance with the present invention, is part of the viruses, may also comprise a nucleic acid sequence mediating the transport of YB-1 into the nucleus.
  • the nucleic acids, viruses and viral systems in accordance with the invention as well as the adenoviruses known in the prior art such as, for example, Onyx-015, Ad ⁇ 24, dl922-947, E1Ad/01/07, CB016, dl 520 and the adenoviruses described in patent EP 0 931 830, can be used as such or in combination with these nucleic acids in accordance with the invention in connection therewith as adenoviruses and adenoviral systems and thus as the corresponding nucleic acids.
  • Suitable nucleic acid sequences which mediate nucleus transport are known to the ones skilled in the art and, for example, described in (Whittaker, G. R. et al., Virology, 246, 1-23, 1998; Friedberg, E. C., TIBS 17, 347, 1992; Sans, D. A. et al., Bioessays 2000 June; 22(6): 532-44; Yoneda, Y., J. Biochem. (Tokyo) 1997 May; 121(5): 811-7; Boulikas, T., Crit. Rev. Eukaryot. Gene Expr. 1993; 3(3): 193-227; Lyons R H, Mol. Cell. Biol., 7, 2451-2456, 1987).
  • YB-1 is formed as a fusion protein together with a signal peptide and is introduced into the nucleus and that the replication of the adenoviruses according to the present invention thus occurs.
  • YB-1 can be provided with a transporter sequence which, preferably starting from synthesis in the cytoplasma, introduces YB-1 into the cell nucleus or which translocates YB-1 into the cell nucleus, and promotes viral replication there.
  • a particularly effective nucleic acid sequence mediating nucleus transport is the TAT sequence of HIV which is, among other suitable nucleic acid sequences of that type described in Efthymiadis, A., Briggs, L J, Jans, D A., JBC 273, 1623-1628, 1998.
  • the adenoviruses which are used in accordance with the present invention comprise nucleic acid sequences which code for peptides coding for nuclear transportation.
  • YB-1 is present in its full length, particularly in a form which corresponds to the wildtype of YB-1. It is within the present invention that YB-1 is used or present as a derivative, such as, e.g. in shortened or truncated form.
  • a YB-1 derivative as used or present within the present invention is a YB-1 which is capable of binding to the E2-late promoter and thus activates gene expression of the adenoviral E2 region.
  • Such derivatives particularly comprise the YB-1 derivatives disclosed herein. Further derivatives may be generated by deletion of single or several amino acids at the N-terminus, at the C-terminus or within the amino acid sequence.
  • YB-1 fragments are also used and referred to as YB-1 proteins in the meaning of the present invention.
  • Various YB-1 fragments are disclosed in the paper of Jürchott K et al. [JBC 2003, 278, 27988-27996] which are characterized by deletions in the C-terminus and the N terminus.
  • the distribution of the various YB-1 fragments indicated that both the cold-shock domain (CSD) as well as the C-terminus are important for the cell cycle-regulated transport of YB-1 into the nucleus.
  • CSD cold-shock domain
  • a truncated YB-1 (which is also referred to herein as YB-1 protein) is migrating in a better way into the nucleus in combination with the expression of E1B55k and E4orf6 in accordance with the present invention and thus induces a stronger CPE without necessarily binding better to the E2-late promoter compared to native YB-1, whereby it cannot be excluded that also a truncated YB-1 is migrating better into the nucleus and exhibits both activities, i.e. induces CPE and binds to the E2-late promoter.
  • truncated YB-1 fragments can also migrate into the nucleus better and bind to the E2-late promoter better without inducing a better CPE. It is also within the present invention that truncated YB-1 proteins or fragments comprise further sequences such as described herein in connection with the full length YB-1, in particular cellular localization signal sequences (NLS) and the like.
  • NLS cellular localization signal sequences
  • the medicament for the manufacture of which the viruses are used in accordance with the present invention represents in its various embodiments a further aspect of the present invention in itself.
  • the invention is related in a further aspect to a method for the screening of patients which, preferably suffer or are suspect to suffer from a tumour or tumour disease and which may be treated using the viruses in accordance with the present invention, whereby the method comprises the following steps:
  • YB-1 instead of or in addition to YB-1 also the presence of the afore-described markers which, preferably, act or are known to act as surrogate markers, can be assessed.
  • the sample can be tested whether the cells contained therein are resistant in the meaning of the present invention.
  • the viruses as disclosed herein may be used in accordance with the present invention.
  • the analysis of the tumor tissue occurs by means of an agent which is selected from the group comprising antibodies against YB-1, YB-1 specifically binding peptides, aptamers against YB-1, aptamers against YB-1, aptamers against YB-1 as well as anticalines against YB-1.
  • an agent which is selected from the group comprising antibodies against YB-1, YB-1 specifically binding peptides, aptamers against YB-1, aptamers against YB-1, aptamers against YB-1, aptamers against YB-1, aptamers against YB-1 as well as anticalines against YB-1.
  • the same kind of agents can also be made and used, respectively, for the respective markers.
  • the manufacture of antibodies, in particular monoclonal antibodies, is known to the ones skilled in the art.
  • a further agent for specific detection of YB-1 or the markers are peptides which bind with a high affinity to their target structures, in the present case
  • phage-display in order to generate such peptides.
  • a peptide library whereby the individual peptides have a length of about 8 to 20 amino acids and the size of the library is about 10 2 to 10 18 , preferably 10 8 to 10 15 different peptides.
  • a particular form of target molecule binding polypeptides are the so-called anticalines which are, for example, described in German patent application DE 197 42 706.
  • a further agent for specifically binding to YD-1 or to the corresponding alternative markers disclosed herein and thus for the detection of a cell cycle independent localisation of YB-1 in the nucleus are the so-called aptamers, i.e. D-nucleic acids, which, based on RNA or DNA, are present as either a single strand or a double strand and specifically bind to a target molecule.
  • aptamers i.e. D-nucleic acids, which, based on RNA or DNA, are present as either a single strand or a double strand and specifically bind to a target molecule.
  • the generation of aptamers is, for example, described in European patent EP 0 533 838.
  • a special embodiment of aptamers are the so-called aptazymes which, for example, are described by Piganeau, N. et al. (2000), Angew. Chem. Int. Ed., 39, no.
  • aptamers are a particular embodiment of aptamers insofar as they comprise apart from the aptamer moiety a ribozyme moiety and, upon binding or release of the target molecule binding to the aptamer moiety, the ribozyme moiety becomes catalytically active and cleaves a nucleic acid substrate which goes along with generation of a signal.
  • a further form of the aptamers are the so-called aptamers, i.e. target molecule binding nucleic acids which consist of L-nucleic acids.
  • spiegelmers i.e. target molecule binding nucleic acids which consist of L-nucleic acids.
  • the method for the generation of such aptamers is, for example, described in WO 98/08856.
  • the sample of the tumor tissue can be obtained by punctuation or surgery.
  • the assessment whether YB-1 is located in the nucleus independent of the cell cycle is frequently done by the use of microscopic techniques and/or immunohistoanalysis, typically using the antibody or any of the further agents described above. Further methods for the detection of YB-1 in the nucleus and that its localisation there is independent of the cell cycle, are known to the one skilled in the art. For example, localisation of YB-1 can easily be detected when scanning tissue slices stained against YB-1. The frequency of YB-1 being in the nucleus is already an indication that the localisation in the nucleus is independent of the cell cycle.
  • a further possibility for cell cycle independent detection of YB-1 in the nucleus is the staining against YB-1 and assessment whether YB-1 is localised in the nucleus and determining the phase of the cells.
  • This and the detection of YB-1 can also be performed using the afore-mentioned agents directed against YB-1.
  • the detection of the agents is done by procedures known to the one skilled in the art. Because said agents are specifically directed against YB-1 and insofar do not bind to other structures within the sample to be analysed, particularly other structures of the cells, both the localisation of said agents by means of a suitable labelling of the agents and due to their specific binding to YB-1, also the localisation of YB-1 can be detected and assessed accordingly. Methods for the labelling of the agents are known to the ones skilled in the art.
  • viruses described herein may also be used in connection with diseases, in particular tumor diseases and more preferably tumor diseases where at least part of the tumor cells exhibit a multiple resistance, in particular a multidrug resistance, whereby YB-1 is present in a deregulated form.
  • diseases in particular tumor diseases and more preferably tumor diseases where at least part of the tumor cells exhibit a multiple resistance, in particular a multidrug resistance, whereby YB-1 is present in a deregulated form.
  • diseases in particular tumor diseases and more preferably tumor diseases where at least part of the tumor cells exhibit a multiple resistance, in particular a multidrug resistance, whereby YB-1 is present in a deregulated form.
  • viruses in accordance with the present invention and as disclosed herein are preferably adenoviruses
  • the insights, methods and uses, nucleic acids, proteins, replication systems and the like are not limited to adenoviruses but apply to other viruses and viral systems.
  • the adenoviruses which are used in accordance with the present invention and the nucleic acids coding therefore, respectively, is any corresponding adenoviral nucleic acid which result in a replication event per se or in combination with further nucleic acid sequences. It is possible, as explained herein, that by means of helper viruses the sequences and/or gene products are provided which are necessary for replication. To the extant it is referred to coding nucleic acid sequences and to the extent they are nucleic acid sequences which are known, it is within the present invention that not only the identical sequence, but also sequences derived therefrom, are used.
  • Derived sequences are in particularly those sequences which still result in a gene product, either nucleic acid or a polypeptide having a function which corresponds to one or the function, of the non-derived sequence. This can be determined by simple routine tests known to the one skilled in the art.
  • An example for such derived nucleic acid sequences are nucleic acid sequences which code for the same gene product, in particularly the same amino acid sequence, however, due to the degeneracy of the genetic code, exhibit a different base sequence.
  • viruses in accordance with the present invention are present as replication systems with or without helper viruses.
  • adenoviral nucleic acid and/or the nucleic acid is present as a replicable vector.
  • nucleic acid(s) coding for the adenoviruses which are used in accordance with the present invention, are present in an expression vector and that this expression vector is used in accordance with the present invention.
  • the present invention is related also to a vector group comprising at least two vectors, whereby the vector group in its entirety comprises an adenoviral replication system as described herein, and the vector group is used in accordance with the present invention. It is within the invention that each of the components of the adenoviral replication system is present on a separate vector, preferably an expression vector.
  • the present invention is related in a further aspect to the use of a cell which contains one or several of the nucleic acids which code for the viruses which are used in accordance with the present invention, and which are to be used in accordance with the invention of and/or a corresponding viral replication system and/or a corresponding vector and/or a vector group according to the invention, for the very same purpose as described herein for the various adenoviruses.
  • viruses and in particular their nucleic acids and the nucleic acids coding therefor may also be introduced in a multipartite form into a cell, preferably a tumour cell, whereby due to the presence of the various individual components they act together as if the individual components were derived from a single nucleic acid and a single or several viruses, respectively.
  • nucleic acids which are used in accordance with the invention and which code for viruses, viral systems or parts thereof, may also be present as vectors.
  • these vectors are viral vectors.
  • the nucleic acids comprise viral nucleic acids
  • the virus particle is the vector. It is, however, also within the present invention that said nucleic acids are present in a plasmid vector.
  • the vector comprises elements which allow for and control the propagation of inserted nucleic acid, i.e. replication and the optional expression of the inserted nucleic acid.
  • Suitable vectors, preferably expression vectors, and respective elements are known to the ones skilled in the art and, for example, described in Grunhaus, A., Horwitz, M. S., 1994, Adenoviruses as cloning vectors. In Rice, C., editor, Seminars in Virology, London: Saunders Scientific Publications.
  • a vector group consists of at least two vectors. Apart from that, any statements made in relation to the vectors is also applicable to the vectors and the vector group, respectively.
  • viruses and in particular adenoviruses, used in accordance with the present invention are characterised by the various nucleic acids and gene products, respectively, disclosed herein and may otherwise preferably comprise all those elements known to the ones skilled in the art and which are inherent to the wildtype adenoviruses (Shenk, T.: Adenoviridae: The virus and their replication. Fields Virology, vol. 3, editors Fields, B. N., Knipe, D. M., Howley, P. M. et al., Lippincott-Raven Publishers, Philadelphia, 1996, chapter 67).
  • the present invention is related to a method for the treatment of tumor diseases comprising the administration of a virus in accordance with the present invention, such nucleic acid, vectors, replication systems, medicaments or pharmaceutical compositions.
  • the tumor disease is one as disclosed herein.
  • the patient is in need of such treatment and is preferably a patient selected from the groups of patients disclosed herein.
  • the features and embodiments disclosed for the respective viruses, nucleic acid, vectors, replication systems, medicaments and pharmaceutical compositions, each in accordance with the present invention are also applicable to each and any of the other aspects of the present invention.
  • the various transgenes can be cloned into appropriate sites within the viral genome. Particularly preferred are the E1-, E2A-, E2B-, E3- and E4-region. The cloning of the transporter into the E1 region is particularly preferred. It will be acknowledged by the one skilled in the art that the cloning of the transgenes into the respective sites of the viral genome will partially or completely inactivate or delete the genes encoded by these sites. However, it is within the present invention that the genes encoded by the particular site can remain partially or completely active.
  • viruses in accordance with the present invention are preferably adenoviruses.
  • treatment of a disease or disorder comprises in a preferred embodiment also the prevention of this disease or disorder.
  • FIG. 1 shows the structural design of the adenoviral vectors referred to as AdE1/E3-minus herein which are E1/E3-deleted adenoviruses, of wildtype adenovirus and adenovirus dl520.
  • FIG. 2 shows the binding domains of the E1A protein with regard to the binding of p300, p107 and p105.
  • FIG. 3 shows U2OS cells which do not have YB-1 in the nucleus, after infection with the E1/E3-deleted adenoviruses Ad5, referred to as E1/E3-minus Ad5, and dl520.
  • FIG. 4 shows 257RDB cells which have YB-1 in the nucleus, after infection with the E1/E3-deleted adenoviruses Ad5, referred to as E1/E3-minus Ad5, and adenovirus dl520.
  • FIG. 5 shows 257RDB cells and U2OS cells after infection with adenovirus dl1119/1131.
  • FIG. 6 shows the result of an EMSA analysis which confirms that YB-1 is present in multidrug resistant cells and cell lines 257RDB, 181 RDB, MCF-7Ad, respectively, whereas YB-1 is not present in the nucleus of U2OS and HeLa cells.
  • FIG. 7 shows the structural design of the E1A protein of wildtype adenovirus, of adenovirus dl520 and adenovirus dl1119/1131.
  • FIG. 8 is a column diagram showing the replication efficiency of adenoviruses in the presence of additionally expressed viral proteins in absolute figures.
  • FIG. 9 is a column diagram showing the increase of replication efficiency of adenoviruses in the presence of additionally expressed viral proteins.
  • FIG. 10 shows wells grown with U2OS cells after crystal violet staining and infection with dl520 with 10 and 30 pfu/cell, respectively, and control (K) without administration of daunorubicine and with the administration of 40 ng daunorubicine per ml, respectively.
  • FIG. 11 shows wells grown with HeLa cells, after crystal violet staining and infection with dl520 and 10 and 30 pfu/cell and control (K), respectively, without administration of daunorubicine and administration of 40 ng daunorubicin per ml, respectively.
  • FIG. 12 is a diagram of the tumor volume of tumors having different origins (RDB257 and HeLa) as a function of time after treatment with PBS and dl520, respectively.
  • FIG. 13 shows pictures of sacrificed mice which developed a tumor based on RDB257 cells after treatment with PBS and 5 ⁇ 10 8 pfu dl520, respectively.
  • FIG. 14 is the result of a Southern Blot analysis of a cell extract (of the tumors grown subcutaneously) of RDB257 cells and HeLa cells after infection with dl520.
  • FIG. 15 is a column diagram showing the replication efficiency and particle formation, respectively, of dl520 and wildtype adenoviruses in YB-1 nucleus-positive tumor cells (257RDB and 181RDB) and YB-1 nucleus-negative tumor cells (HeLa, U2OS).
  • FIG. 16 shows the structural design of wildtype adenovirus and adenoviral vector AdXvir03.
  • FIG. 17 shows the structural design of adenoviral vector AdXvir03/01.
  • FIG. 18 A/B shows wells grown with 181RDB cells ( FIG. 18A ) and 272RDB cells ( FIG. 18B ) after crystal violet staining and infection with Ad312 (20 pfu/cell), Xvir03 (5 pfu/cell) and control (non-infected), whereby crystal violet staining was performed five days past infection;
  • FIG. 19 is the result of a Southern blot analysis of the replication behaviour of adenovirus dl 520 in U373 cells with and without treatment of the cells with irinotecan;
  • FIG. 20 is the result of a Southern blot analysis of the replication behaviour of adenovirus dl 520 in U373 cells with and without treatment of the cells with trichostatin A;
  • FIG. 21 is the result of a FACS analysis of trichostatin treated U 373 cells related to the expression of the Coxsackie virus adenovirus receptor (CAR), expressed as percentage of CAR positive cells; and
  • FIG. 22 shows four different panels of cell layers for depicting the effect of replicating adenovirus dl520 and irinotecan and trichostatin in different combinations;
  • FIG. 23 shows a schematic representation of the ORF of E1B 55K with the 3′UTR fragment and the restriction cleavage site Bfr I at position 3532;
  • FIG. 24 shows the sequence of the E1B55k-3′UTR region corresponding to sequence position 3507 to 4174 of wildtype Ad 5;
  • FIG. 25 shows the result of a Northern blot analysis of the expression of the E2 gene in A549 cells and U2OS cells after infection with wildtype adenovirus Ad5 and adenovirus Ad312;
  • FIG. 26 shows the result of a Northern blot analysis of the expression of the E2 gene in U2OS cells after infection with wildtype adenovirus and adenovirus delta24 after 12 and 24 hours;
  • FIG. 27 shows the structural design of the adenoviral vector XvirPSJL1
  • FIG. 28 shows the structural design of the adenoviral vector XvirPSJL2
  • FIG. 29 shows wells with HeLa cells grown therein after crystal violet staining and infection with adenovirus dl520 using different pfu/cells;
  • FIG. 30 shows a bar graph indicating the activity of luciferase in U2OS cells, HeLa cells and 257RDB cells upon usage of different promoter fragments of the adenoviral E2-late promoter;
  • FIG. 31 shows a bar graph indicating the number of viral particles after infection of U2OS cells with a YB-1 expressing adenovirus and virus Ad312 after two and five days, whereby a distinction is made between intracellularly remaining viral particles (represented in black) and released extracellular viral particles (horizontally striped);
  • FIG. 32 shows schematic representation of the regulation of the E2 region of adenovirus by the E2-late and E2 early promoters by E2F and YB-1;
  • FIG. 33 shows the schematic design of wildtype adenovirus
  • FIG. 34 is a schematic representation of the adenovirus Xvir 05/promoter in accordance with the present invention which expresses protein IX under the control of the E2 late promoter;
  • FIG. 35 is a schematic representation of the adenovirus Xvir 05/E1A12S in accordance with the present invention which expresses the protein IX as part of the E1B55K reading frame under the control of E1A12S;
  • FIG. 36 is a schematic representation of an adenovirus Xvir 05E1B19K in accordance with the present invention, which expresses protein IX under the control of E1B19K;
  • FIG. 37 is a schematic representation of the adenovirus Xvir 05/E3-IX promoter in accordance with the present invention which expresses protein IX under the control of the E3 promoter;
  • FIG. 38 is a schematic representation of the wildtype adenovirus and the adenovirus Xvir 05 in accordance with the present invention which is an embodiment of virus Xvir 05/E1B19K;
  • FIG. 39 is a schematic representation of wildtype adenovirus and the adenovirus Xvir 05/protein IX in accordance with the present invention which is an embodiment of the virus Xvir 05/E1A12S;
  • FIG. 40 is a schematic representation of the wildtype adenovirus and the adenovirus Xvir 05/01 in accordance with the present invention which is an embodiment of the virus Xvir 05/protein IX;
  • FIG. 41 is a schematic representation of the wildtype adenovirus and the adenovirus Xvir 05/02 in accordance with the present invention which is an embodiment of the virus Xvir 05/protein IX;
  • FIG. 42 shows the result of a Northern blot analysis for the detection of protein IX.
  • FIG. 43 shows the result of a Southern blot analysis of Xvir03-3′UTR
  • FIG. 44 shows the result of the MRP expression using Northern blot analysis after infection with Xvir03-3′UTR
  • FIG. 45 shows the result of the MDR expression using Northern blot analysis after infection with Xvir03-3′UTR
  • FIG. 46 shows the result of the MRP expression using Northern blot analysis after infection with Xvir03-3′UTR
  • FIG. 47 shows wells grown with DU145 cells after crystal violet staining and infection with adenovirus Xvir03 with different pfu/cells;
  • FIG. 48 shows wells grown with PC-3 cells after crystal violet staining and infection with adenovirus Xvir03 using different pfu/cells;
  • FIG. 49 shows four different panels of cell layers for illustrating the effect of replicating adenovirus Xvir03 and daunorubicin.
  • FIG. 50 shows the structural design of adenoviral vectors Xvir03 and Xvir03-3′UTR, respectively.
  • FIG. 1 shows the structural design of adenoviral vectors AdE1/E3-minus, i.e. E1/E3-deleted adenoviruses, wildtype adenovirus and adenovirus dl520.
  • Adenovirus AdE1/E3-minus does not have a region coding for a functional E1A or a functional E1B or E3 and is used in the present experiments as a control for toxicity.
  • Wildtype E1A gene codes for a total of 5 proteins which are generated through alternative splicing of the E1A RNA. Among others, two different proteins are generated, namely a 289 amino acid protein and a 243 amino acid protein. dl520 does not code for the 289 amino acid protein as it has a deletion in the CR3 stretch of the E1A gene which results in the lack of the 13S gene product.
  • the adenovirus dl520 which may be used in accordance with the invention is referred to as 12S-E1A virus by those skilled in the art.
  • Adenovirus dl347 (Wong and Ziff, J. Virol., 68, 4910-4920, 1994) known in the prior art is also a 12S-E1A virus which can be used in accordance with the present invention.
  • CR1, CR2 and CR3 regions which are conserved among various adenoviral subtypes. These are referred to as CR1, CR2 and CR3. While CR1 and CR2 are present in both E1A proteins (E1A 12S and E1A 13S), i.e. in both the 289 amino acid and the 243 amino acid protein, the CR3 region is only present in the bigger one of the two aforementioned proteins.
  • the CR3 region is required for the activation of viral genes, in particular of E1B, E2, E3 and E4.
  • Viruses which only comprise the smaller, i.e. 243 amino acid protein are only very weakly transactivating the viral genes and do not promote adenoviral replication in those cells which do not have YB-1 in the nucleus.
  • YB-1 is present in the nucleus only in tumor cells and can be detected only there, this vector is suitable to induce tumor-specific replication.
  • this adenovirus cannot translocate cellular YB-1 into the cell's nucleus which is also referred to herein as translocation, and is thus not in a position to replicate in cells which are YB-1 nucleus-negative and is thus a virus which can be used in accordance with the present invention, whereby this virus comprises the transactivation required in accordance with the present invention.
  • FIG. 2 shows the binding domains of the E1A protein with regard to the binding of p300, p107 and p105.
  • P300 as well as p107, is a cellular binding protein.
  • pRb and p107/p300 are in combination with the cellular transcription factor E2F effective in regulating transcription.
  • the wildtype E1A protein interferes with the binding of E2F to Rb.
  • the thus released E2F binds to the E2 early promoter and induces adenoviral replication thereby.
  • the adenoviral vector dl922-947 comprises a deletion in the CR2 region (amino acid positions 122-129) and the vector CB016 has deletions in the CR1 region (amino acid positions 27-80) and CR2 region (amino acid positions 122-129).
  • the vector E1Adl01/07 comprises a deletion in the CR2 region (amino acid positions 111-123).
  • the adenoviral vector Ad ⁇ 24 comprises a deletion in the CR2 region (amino acid positions 120-127).
  • the adenoviral vector described in patent EP 0 931 830 comprises deletions in the CR1 region and CR2 region.
  • E2F/RB and the release of E2F mediated through E1A is fundamentally different from the mechanism underlying the present invention. Unlike assumed in the prior art it is not the release of E2F from the Rb protein which is essential, not to say critical for viral replication, but it is the nuclear localisation of the human transcription factor YB-1. This transcription factor is, in normal cells, only present in the cytoplasm over most of the cell cycle.
  • tumor diseases including, for example, but not limited thereto, breast cancer, ovary carcinoma, prostate carcinoma, osteosarcoma, glioblastoma, melanoma, small cell lung carcinoma and colorectal carcinoma.
  • the U2OS cells which do not have YB-1 in the nucleus show no lysis as illustrated by crystal violet staining after infection with two different adenoviruses, namely the E1/E3-deleted adenovirus referred to as E1/E3-minus, and adenovirus dl520, which can be used in accordance with the present invention.
  • E1/E3-minus E1/E3-deleted adenovirus
  • adenovirus dl520 which can be used in accordance with the present invention.
  • the medium is removed.
  • the cells are overlaid with crystal violet (50% ETON, 3% formaldehyde, 5% acetic acid, 1% crystal violet) and incubated at room temperature for 5-10 min.
  • the plates having 6 wells are thoroughly rinsed with water and dried at room temperature.
  • 100,000 257RDB cells were plated per well. On the next day the cells were infected with the various adenoviruses as depicted in FIG. 4 . The infection was performed in 500 ⁇ l serum free DMEM medium for 1 h at 37° C. Subsequently, the infection medium was removed and replaced by 2 ml complete medium (10% FCS/DMEM). The analysis was performed after three days using crystal violet staining.
  • E1/E3-minus Ad5 which is E1/E3-deleted
  • dl520 which, as shown in example 3, does not replicate in YB-1 nucleus-negative cells and at the same time codes with E1A for a transactivating oncogene protein in accordance with the present invention, results in a factually complete lysis at an MOI (multiplicity of infection) of 40 pfu per cell and a still predominant lysis at an MOI of 10 pfu per cell.
  • dl520 and similar viruses such as described herein by dl1119/1131 or AdXvir 03, require an MOI which is reduced by about 1 magnitude (factor of ten) compared to E1-deleted or an E1/E3-deleted adenovirus which justifies their clinical use.
  • the protein E1A of dl520 is characterised in that the CR3 region thereof is deleted which results in the transactivation required for the use in accordance with the present invention and replication in YB-1 nucleus-positive cells.
  • the adenovirus dl1119/1131 is thus a further adenovirus which can be used in accordance with the present invention. It is within the present invention that also viruses can be used which are designed similar to dl1119/1131 with regard to the CR3 region, but, in contrast thereto, have the CR1 region and/or CR2 region.
  • nuclear YB-1 should bind as a transcription factor to the Y-box (CAAT sequence) within the mdr1 promoter (engl. multiple drug resistance promoter).
  • EMSA analysis electrospreading assay
  • nuclear protein is isolated and subsequently 1-10 ⁇ g protein is incubated together with a short DNA fragment (oligo) at 37° C.
  • oligo short DNA fragment
  • the following oligonucleotide was used: mdr1 promoter in contrast to U203 (Position ⁇ 86 to ⁇ 67): TGAGGCTGATTGGCTGGGCA (SEQ. ID: No. 1) (the X-box is underlined).
  • This DNA fragment is radioactively labelled at the 5′ end with 32 P prior to that. Subsequently, separation is performed in a native polyacryl amide gel. In case the protein YB-1 is binding to a sequence in the oligonucleotide, this can be detected as any non-bound oligonucleotide is migrating faster in the gel than bound oligonucleotide (Holm, P. S. et al., JBC 277, 10427-10434, 2002; Bargou, R. C. et al., Nature Medicine 3, 447-450, 1997).
  • YB-1 is present in the nucleus of multidrug resistant cells 257RDB, 181RDB and MCF-7Ad cells in contrast to cell lines U2OS and HeLa cells.
  • results shown in example 4 and 5 confirm that the adenoviruses dl520 and dl1119/1131 replicate in YB-1 nucleus-positive cells such as, e.g., 257RDB in contrast to U205, and induce lysis thereof. This confirms the finding about the use of the adenoviruses in accordance with the present invention.
  • results confirm that already a, compared to wildtype adenovirus, weak transactivation of viral genes in YB-1 nucleus-positive cells through modified or deleted E1A gene products results in successful replication and lysis of such cells in the presence of YB-1 in the nucleus, including, for example, multidrug resistant cells and that the adenoviruses as described herein, can thus be used in the lysis of such tumors.
  • Ad-55K is an E1/E3 deleted virus, whereby E1B-55K is cloned into E1 and is under the control of CMV (Dobbelstein, M. et al., EMBO Journal, 16, 4276-4284, 1997). This substitution is necessary with regard to the fact that AdYB-1, i.e.
  • an adenovirus which expresses YB-1 does not express these early genes and that the present inventor has recognised that a substitution of these early genes in a replication system which contains YB-1 in the nucleus, is capable of increasing replication efficiency and particle formation efficiency, respectively, to an extent comparable to the one of wildtype adenoviruses of type Ad5.
  • the plasmid pE4orf6 carries the DNA sequence coding for the early viral gene E4orf6 under the control of CMV.
  • Ad-55K is an E1/E3-deleted virus which carries as transgene the viral gene E1B-55K under CMV control.
  • FIGS. 8 and 9 show the result of the plaque assay, represented in absolute figures. The most significant difference compared to infection with AdYB-1 alone is shown by transfection with the plasmid pE4orf6 and co-infection with the two viruses AdYB-1 and Ad-55K.
  • FIG. 8 shows the result of the plaque assay, represented in absolute figures. The most significant difference compared to infection with AdYB-1 alone is shown by transfection with the plasmid pE4orf6 and co-infection with the two viruses AdYB-1 and Ad-55K.
  • FIG. 9 shows the result of FIG. 8 , whereby the increase of the replication efficiency is represented as multifold of the replication determined for AdYB-1.
  • YB-1 localised in the nucleus controls adenoviral replication by means of activation of the adenoviral E2-late promoter. The combination of both effects can be used in order to provide for specific tumor lysis.
  • daunorubicine induces the replication of dl520 through nuclear localisation of YB-1.
  • dl520 creates a bigger tumorlytic effect in combination with the cytostatic daunorubicine compared to daunorubicine alone.
  • the HeLa (YB-1 nucleus-negative) and 257RDB (YB-1 nucleus-positive) cells used in this in vivo study were expanded under sterile cell culture conditions. Prior to the injection of the cells into mice (strain CD1NuNu) in order to generate a subcutaneous tumor, the cells are harvested by trypsinisation, taken up in DMEM medium (10% FCS), counted and washed with PBS one time. Subsequently, the cells are centrifuged, the PBS aspired and the cells are portioned in fresh PBS with the desired cell number. The cell number which was subcutaneously injected in this study, was each 5 ⁇ 10 6 cells of both cell lines.
  • the injection was performed subcutaneously into one flank of the animals, whereby HeLa cells were injected into the right side and 257RDB cells were injected into the left side for better distinction.
  • the growth of the tumors was controlled twice a week and thereby the length and the width of the tumors was measured using vernier calipers. Based thereon, the tumor volume was calculated based on the following mathematical formula:
  • the virus and PBS as negative control, respectively were intratumorally applied.
  • the volumes to be injected were identical and were 50 ⁇ l each time. This was repeated on 3 consecutive days.
  • the overall dosage of applied viruses was 5 ⁇ 10 8 pfu.
  • the tumor growth was continued to be documented twice a week and the volume was calculated.
  • the mice were sacrificed and the tumors removed for further analysis.
  • FIG. 12 shows a diagram representing the tumor volume as a function of time and the various treatment schemes.
  • the tumor was formed by RDB257, there was a significant growth of the tumor to about 438 mm 3 to 1466 mm 3 upon injection of PBS.
  • the vector dl520 which was used in accordance with the invention, tumor growth could be reduced significantly. Starting from a mean tumor size of 344 mm 3 , the tumor size increased only by 21% to a total of 543 mm 3 .
  • the tumor consisting of HeLa cells was used as a control which upon administration of PBS behaved similarly to the RDB257 based tumor upon administration of PBS.
  • Tumors based on HeLa cells and treated with dl520 still showed a significant increase in tumor growth starting from 311 mm 3 and increasing to 1954 mm 3 .
  • FIG. 13 shows a picture of the sacrificed nude mice which had a tumor grown using RDB257. It can be clearly seen that after the application of adenovirus dl520 in accordance with the present invention a significant reduction of the tumor occurred. In the present case there was even a reduction in the tumor volume (day 1 after administration of virus dl520: 515 mm 3 ; day 30 after administration of virus dl520: 350 mm 3 ).
  • DNA was extracted from a tumor sample which has been taken from the middle of the tumor developed in example 9.
  • the Dneasy Tissue Kit of Qiagen is used for isolation. The DNA isolation is done in accordance with manufacturer's instructions. In accordance therewith, the DNA was released from the cells through alkaline lysis. Subsequently, the isolated DNA is purified over a column. Subsequently, the concentration of the isolated DNA is determined by photometry at 260 nm. The analysis was performed using 2 ⁇ g of the DNA samples which were digested with 10 units of restriction enzyme Kpn I. Subsequently, an electrophoretic separation of the samples was performed in a 0.8% agarose gel.
  • the DNA was blotted onto a nylon membrane (performed according to the system of Schleicher & Schuell).
  • the DNA blotted onto the membrane is hybridised against a specific 1501 bp DNA probe.
  • the 1501 bp DNA probe specifically binds to the 3369 bp Kpn I fragment within the E2A coding Ad5 sequence.
  • the probe was prepared prior to that by PCR (primer: 5′-GTC GGA GAT CAG ATC CGC GT (SEQ. ID. No. 2), 5′-GAT CCT CGT CGT CTT CGC TT (SEQ. ID. No. 3)) and radioactively labelled using 32 P.
  • the membrane is washed and exposed to a film.
  • FIG. 14 The result of the Southern Blot of tumor DNA is depicted in FIG. 14 .
  • the analysis confirms that only dl520 replicates in vitro in resistant cells RDB257, as depicted in lanes 3, 4 and 5.
  • Lane 1 shows as positive control Ad-5d
  • lane 6, 7 and 8 show DNA from HeLa cells which were infected with dl520.
  • HeLa cells are not YB-1 nucleus positive the virus dl520 did not replicate so that, in accordance therewith, the E2A sequence could not be detected.
  • FIG. 15 A further result with dl520 is depicted in FIG. 15 .
  • the particle formation (pfu/ml) was investigated after infection with dl520 and wildtype adenovirus.
  • Various YB-1 nucleus-positive (257RDB and 181RDB) tumor cells and YB-1 nucleus-negative tumor cells were infected with dl520 and wildtype adenovirus.
  • the result of the plaque assay shows that dl520 is replicating in YB-1 nucleus-positive cells (257RDB and 181RDB) similar to wildtype adenovirus. Insofar a replication efficiency can be observed similar to the one of wildtype adenoviruses when using, in accordance with the present invention, the adenoviruses described herein.
  • FIG. 16 shows the structural design of the adenoviral vector Xvir03.
  • the adenovirus Xvir03 is a so-called E1/E3-deleted adenovirus. This means that no E1A, E1B (E1B55k and E1B19K proteins) and E3 proteins are manufactured which are functional in adenoviral replication.
  • the deletion of the E1 region extends from 342-3528; the deletion of the E3 region of the base position 27865-30995.
  • the term “E1-deleted virus” means a virus in which E1 is no longer functionally active.
  • E1 region coding proteins having various sizes.
  • E4 region such as E4orf6
  • the viral genes E1B55k and E4orf6 are expressed in the E1 region by means of the heterologous CMV promoter (Clontech: Plasmid pShuttle) introduced into Xvir03. Instead of the CMV promoter each and any of the promoters as disclosed herein in connection with the expression of E1A can be used.
  • IRES sequence engl. internal ribosomal entry site
  • pCITE novagen: pCITE
  • the Vector was Manufactured as followss: System Adeno-X of the Company Clontech
  • E1B55k-pShuttle The plasmid E1B55k-pShuttle was created by cloning the open reading frame of E1B55k from pCGNE1B from M. Dobelstein (University of Marburg) with XbaI and BfrI into the pShuttle vector from Clontech and only BamH I, whereby in this case the ends are made blunt ended and cloned into the blunt ended pShuttle. Subsequently, E1B55k in pShuttle was linearised with ApaI, the ends blunt ended and cut with NheI.
  • the fragment IRES-E4orf6 was linked with the open vector E1B55k-pShuttle (blunt, NheI).
  • the cassette was subsequently cloned from the E1B55k-IRES-E4orf6-pShuttle together with the CMV promoter and the bovine growth hormone (BGH)-PolyA into the ⁇ E1, ⁇ E3 Adeno-X-Plasmid (Clontech) with I-Ceu I and PI-SceI, and referred to as AdcmvE1B/IRES/E4orf6. Subsequently, the adenovirus was made in accordance with manufacturer's instructions (Clontech).
  • the adeno plasmid which was linearised with Pad having the expression element CMV-E1B55k-IRES-E4orf6-BGH polyA was transfected into HEK293 cells and 11 days post transfectionem the ablating cells were removed together with the medium in order to release the adenoviruses through repeated freeze-thaw cycles.
  • adenoviruses may be used for the manufacture of the adenoviruses according to the present invention, preferably the recombinant adenovirus, in particular those which contain, individually and/or together, the cassettes E4orf6-IRES-E1B55k and YB-1-IRES-E1A12S. Additionally, individual transgenes may be exchanged between the cassettes.
  • AdEasy of QBIOGENE and Microbix may be used for the manufacture of the adenoviruses according to the present invention, preferably the recombinant adenovirus, in particular those which contain, individually and/or together, the cassettes E4orf6-IRES-E1B55k and YB-1-IRES-E1A12S. Additionally, individual transgenes may be exchanged between the cassettes.
  • cassette has the following design: E1B55k-IRES-E4orf6 and E1A12S-IRES-YB1.
  • E1/E3 deleted recombinant Adenovirus contains the cassette E4orf6-IRES-E1B55k. It is, however, within an embodiment that the virus comprises only an E1-deletion, which means that the E3-region remains intact. Optionally, the E4-region may be partially and/or completely deleted.
  • E1B55k forward primer 5′-ATGGAGCGAAGAAACCC-3′
  • E1B55k 3′UTR backward primer 5′-CACGTCCTGGAAAAAATACAC-3′
  • the transgene was provided with a hCMV-promoter at the 5′end and with the bovine growth hormone polyadenylation signal at the 3′end.
  • E1B55k is used from the plasmid pCGNE1B from Dobbelstein (Dobbelstein, M. et al., EMBO Journal, 16, 4276-4284, 1997) by means of Bam HI and blunt ending and TA-cloning, respectively.
  • the E1B55k-3′UTR which has been cloned, is, among others, described in more detail in FIGS. 23 and 24 .
  • primers were used for the E4orf6 transgene which create a BamHI cleavage site at the 5′-end and a EcoRI cleavage site at the 3′-end of the open reading frame.
  • the amplificate was digested with the respective restriction enzymes and the ends thereof were made compatible for the directed cloning into the vector which has been opened using BamHI and EcoRI.
  • plasmid E4orf6 in pcDNA3.1(+) was linearized with EcoRV, the T-ends added and the amplificate cloned into the IRES element. After checking the correct orientation of the IRES element, the vector was used for further cloning.
  • p ⁇ E1sp1A As the shuttle vector p ⁇ E1sp1A, now used for the adenoviral generation system of the company Microbix, did neither contain a CMV promoter nor a bovine growth hormone polyadenylation signal, these elements were cloned into p ⁇ E1sp1A.
  • p ⁇ E1sp1A was linearized with ClaI, made blunt ended and cut with EcoRI.
  • the element CMV-MCS (multiple cloning site)-poly-A was linearized from pShuttle (Clontech) with MfeI, the ends made blunt ended and further cut with EcoRI.
  • the cassette (Xvir-3′UTR pShuttle from Clontech) was cloned with PmeI into the CMV-MCS-poly-A p ⁇ E1sp1A vector which had also been cut with PmeI and subsequently diphosphorylated.
  • the cloning product Xvir-3′UTR-p ⁇ E1sp1A was used for virus generation.
  • Xvir-3′UTR-p ⁇ E1sp1A and pBHGE3 (from Microbix, contains the E3-region which corresponds to wildtype adenovirus type 5) was cotransfected into HEK 293 cells, whereupon virus Ad-Xvir-3′UTR E3 was generated due to recombination of homologous sequences of both vectors.
  • Ad-Xvir3′UTR-AdEASY E3 Using the AdEASY-System (Company Qbiogene)
  • the vector pShuttle-AdEASY did neither contain a CMV-promoter nor the bovine growth hormone polyadenylation signal, these elements were cloned into pShuttle-AdEASY.
  • the plasmid was digested with EcoRI, the ends made blunt ended by fling them up with T4-polymerase and dNTPs, the backbone was dephosphorylated and both of the generated digestion products ligated again. By doing so the restriction recognition site for EcoRI was eliminated. The thus resulting plasmid was referred to as pShuttle(-EcoRI)-AdEASY.
  • the cassette CMV-MCS-polyA from the pShuttle of Clontech was cut with MfeI and EcoRI, the ends made blunt ended and cloned into the vector pShuttle (-EcoRI)-AdEASY which was, for such purpose, linearized with XbaI, made blunt ended and dephosphorylated.
  • plasmid CMV-MCS-polyA-pShuttle-AdEASY was generated.
  • the cassette E4Orf6-IRES-E1B55k-3′UTR was cloned into this plasmid using MluI and EcoRI. By doing so the plasmid Xvir-3′UTR in pShuttle AdEASY was generated.
  • the E3 region is substantially deleted in plasmid pAdEASY
  • the E3 region was cloned from plasmid pAdEASY with SpeI and PacI into plasmid CMV-MCS-polyA pShuttle (AdEASY) for reconstruction and thus the plasmid E3E4-pShuttle-AdEASY generated.
  • E3E4-region from the E3E4-pShuttle (-NdeI)-AdEASY was cut with SpeI and Pad and cloned into the pAdEASY and cut with SpeI and Pad, whereby in plasmid pAdEASY the E3-region was re-established (pAdEASY-E3).
  • XVir-3′UTR-pAdEASY-E3 was generated by homologous recombination upon transforming B15183 (EC) bacteria with plasmids Xvir-3′UTR in pShuttle AdEASY and pAdEASY-E3.
  • E4 region in plasmid E3E4-pShuttle (-NdeI)-AdEASY can be deleted specifically.
  • the E4orf6 region is shortened by about 0.6 kB, preferably 629 or 634 bp, by excision with PstI and religation. This can, as described in FIG. 17 , be performed in connection with Xvir03/01. Respective deletions are also feasible by the one skilled in the art in different systems for the generation of recombinant adenovirus.
  • the HI Loop of the fibre knob domain was modified following Dmitriev et al. 1998 (An Adenovirus Vector with Genetically Modified Fibers Demonstrates Expanded Tropism via Utilization of a Coxsackievirus and Adenovirus Receptor-Independent Cell Entry Mechanism): The respective region was amplified using the primers RGD-Hpa fw (5′-GAGgttaacCTAAGCACTGCCAAG-3′), RGD-EcoRV rev (5′-CATAGAGTATGCAGATATCGTTAGTGTTACAGGTTTAGTTTTG-3′) and RGD-EcoRV fw (5′-GTAACACTAACGATATCTGCATACTCTATGTCATTTTCATGG-3′) and RGD-Bfr rev (5′-CAGCGACATGAActtaagTGAGCTGC-3′) and thus an EcoRV restriction site generated.
  • RGD-oligo 1 (5′-CACACTAAACGGTACACAGGAAACAGGAGACACAACTTGTGACTGCCGCGGAGACTGTTTCTGCCC-3′) and RGD-oligo 2 (5′-GGGCAGAAACAGTCTCCGCGGCAGTCACAAGTTGTGTCTCCTGTTTCCTGTGTACCGTTTAGTGTG-3′).
  • RGD motif is present in the HI Loop of the fibre knob domain.
  • the vector described above is in principle suitable as are the other viruses described herein for use in accordance with the present invention.
  • the afore-described vector is suitable to replicate and trigger lysis insofar, in cells which are YB-1 nucleus-positive cells as well as in cells where YB-1 is deregulated, i.e. is overexpressed compared to normal cells and non-tumor cells, respectively.
  • the use of this vector particularly applies to those diseases and groups of patients or collectives of patients which are disclosed in connection with the other adenoviruses which are described herein to be used in accordance with the present invention and the other adenoviruses of the present invention disclosed herein.
  • Xvir03/01 is a further development of Xvir03.
  • Therapeutic genes such as, for example, the genes described herein and the transgene can be cloned into the E3 region. Additionally, a deletion was introduced into the E4 region so as to avoid homologous recombination with the E4orf6 from the expression cassette of Xvir03. This allows that larger transgenes can be cloned in this construct.
  • the deleted E3 region contains SacI, NdeI and NheI restriction sites for introducing a cassette, into which, for example, the therapeutic transgenes can be cloned. However, the E3 may also stayintact and the therapeutic genes be cloned into the E4 region. By doing so the expression of the adenoviral death protein is provided.
  • the pAdenoX-Plasmid of Clontech has a restriction site for SfuI behind the 3′ ITR region which is absent in wildtype adenovirus.
  • the expression cassette was subsequently, as described for Xvir03, cloned with I-Ceu I and PI-SceI from the E1B55k-IRES-E4orf6-pShuttle together with the CMV promoter and the bovine growth hormone (BGH)-PolyA into pAdenoX E3 ⁇ 27865-30995, E4 ⁇ 33241-33875 and referred to as AdcmvE1B/IRES/E4orf6- ⁇ E4. Subsequently, the adenovirus was made in accordance with manufacturer's instructions (Clontech).
  • the afore-described vector is in principle useful as are the other viruses described herein to be used in accordance with the present invention.
  • the afore-described vector is suitable to replicate in YB-1 nucleus-positive cells as well as cells in which YB-1 is deregulated, i.e. is overexpressed compared to normal cells and non-tumor cells, and to cause lysis insofar.
  • This vector can also be used for those diseases and groups of patients and collectives of patients which are disclosed herein for the other adenoviruses to be used in accordance with the present invention and the adenoviruses in accordance with the present invention.
  • the multidrug resistant cells which have YB-1 in the nucleus show lysis after infection with Ad312 and Xvir03 only in case of Xvir03 as represented by the crystal violet staining of the cells.
  • the medium is removed.
  • the cells are covered with crystal violet (50% ETOH, 3% formaldehyde, 5% acetic acid, 1% crystal violet) and incubated at room temperature for 5-10 min.
  • the six well plates are thoroughly rinsed with water and dried at room temperature.
  • E1A-deleted viruses e.g. Ad312
  • Ad312 E1A-deleted viruses
  • MOIs Nevins J. R., Cell 26, 213-220, 1981
  • This phenomenon is referred to in the literature as “E1A-like activity”.
  • the adenovirus Ad312 as used herein, is an E1A-deleted virus.
  • the early adenoviral genes such as E1B55k and E4orf6 are not expressed or expressed only to a very small extent (Nevins J. R., Cell 26, 213-220, 1981). As already described herein, these genes and proteins play an important role in viral replication. In contrast thereto, these genes and proteins, respectively, are expressed by adenovirus Xvir03 ( FIG. 16 ). As may be taken from FIGS.
  • the expression of the genes E1B55k and E4orf6 will result in an efficient viral replication and cell lysis at a concomitantly lower infection titer required (expressed as pfu/cell).
  • the titer required therefor of only 1 to 5 pfu/cell now allows for clinical application.
  • FIG. 19 shows that after incubation with Irinotecan adenoviral replication is significantly increased in U373 cells after treatment with Irinotecan (lane 2) compared to untreated control where no incubation with Irinotecan was performed (lane 1). This means that adenoviral replication is increased under the influence of Irinotecan.
  • Trichostatin A In order to test the effect of Trichostatin A on adenoviral replication, 10 6 U373 tumour cells were plated in 10 cm 2 Petri dishes. After 24 hours 0.25, 0.5 and 0.75 ⁇ M Trichostatin A was added. After another 24 hours the cells were infected with 10 pfu/cell dl520.
  • FIG. 20 shows that after incubation with increasing concentrations of Trichostatin A viral replication in U373 cells (lanes 2, 3 and 4) is significantly increased compared to untreated controls where no incubation with Trichostatin A was performed (lane 1). This means that viral replication is increased under the influence of Trichostatin A.
  • 200,000 U373 cells were plated in a 6 well plate. After 24 hours either 2 ⁇ M Irinotecan or only 1 ⁇ M Trichostatin A or 1 ⁇ M Irinotecan+0.5 ⁇ M Trichostatin were added to the medium. After 24 hours of incubation the cells were infected with 10, 20 and 30 pfu/cell dl520. After 3-5 days the analysis was performed using crystal violet staining. The assays were performed in duplicate.
  • FIG. 22 The result is depicted in FIG. 22 .
  • the six plates represented in panel 1 show a complete cell layer which was not affected by incubation with a combination of Irinotecan and Trichostatin A as shown by crystal violet staining.
  • the next two wells of panel 1 show the cell layer after infection with 10 and 20 pfu/cell dl520, respectively. Also under such conditions there is no lysis of the cells which is due to the absence of replication of dl520. Thus it is shown that neither dl520 at 10 or 20 pfu/cells nor 1 ⁇ M Irinotecan+0.5 ⁇ M Trichostatin A alone are suitable to induce cell lysis.
  • the further 6 well plates 2, 3 and 4 depicted in FIG. 22 were basically treated in accordance with this scheme.
  • the individual wells were inoculated with U373 cells as previously described and the cells cultivated therein.
  • the wells were inoculated with 10, 20 or 30 pfu/cell dl520 in duplicate, whereby the difference between the three 6 well plates resided in the kind of cytostatics used.
  • panel 2 2 ⁇ M Irinotecan
  • in panel 3 1 ⁇ M Trichostatin A
  • panel 4 1 ⁇ M Irinotecan and 0.5 ⁇ M Trichostatin A was added to the individual plates.
  • the test shows that the combination consisting of Irinotecan+Trichostatin A+dl520 induces a more effective cell lyses of tumour cells as any compound alone.
  • Irinotecan translates YB-1 into the cell nucleus and thus induces an improved adenoviral replication.
  • the cellular YB-1 is assisting adenoviral replication after infection with dl520 and is no longer available for DNA-repair processes. Depending on the point of view, this results in an improved efficacy of dl520 on the one hand and an increased efficacy of the cytostatics on the other hand.
  • Ad312 50 pfu/cell
  • Adwt which served as control, 5 pfu/cell
  • the high virus titer of Ad312 resulted in an E1-independent replication in tumor cells.
  • the infection was done in 1-2 ml serum-free DMEM medium for 1 h at 37° C. Subsequently, the infection medium was removed and replaced by 10 ml complete medium (10% FCS/DMEM). After 3 days the RNA was isolated. Subsequently, the concentration of the isolated RNA was measured in a photometer at 260 nm.
  • RNA samples were electrophoretically separated in a 0.8% formaldehyde agarose gel. Subsequently, the RNA was blotted on a nylon membrane (conducted according to the system of Schleicher & Schuell). The RNA blotted on the membrane is blotted against an “early probe” E2 and a “late probe” E2.
  • the 1501 bp “late probe” specifically binds behind the E2-late promoter.
  • the probe was prepared prior to that by PCR (primer: 5′-GTC GGA GAT CAG ATC CGC GT (SEQ. ID. NO. 4), 5′-GAT CCT CGT CGT CTT CGC TT (SEQ. ID. NO.
  • the early probe binds between the E2-early promoter and the E2-late promoter (position: 226791-227002) and was also generated by means of PCR (primer: 5′-AGCTGATCTTCGCTTTTG (SEQ. ID. NO. 6), 5′-GGATAGCAAGACTCTGAC AAAG (SEQ. ID. NO. 7)). Subsequently, the membrane was washed and exposed to a film.
  • Addelta24 adenovirus delta 24
  • Adwt wildtype adenovirus
  • the used recombinant adenovirus Addelta24 has a specific deletion in the CR2 region of the E1A protein and is thus only capable of replicating in Rb-negative tumors. Additionally, the virus expresses the genes E1B55k and E4orf6 comparable to the wildtype adenovirus.
  • the “late probe” comprising 1501 bp, binds specifically behind the E2-late promoter.
  • the probe was prepared prior to that by PCR (primer: 5′-GTC GGA GAT CAG ATC CGC GT (SEQ. ID. NO. 4), 5′-GAT CCT CGT CGT CTT CGC TT (SEQ. ID. NO. 5)) and radioactively labelled using 32 P.
  • the early probe binds between the E2-early promoter and the E2-late promoter and was also prepared by PCR (primer: 5′-AGCTGATCTTCGCTTTTG (SEQ. ID. NO. 6), 5′-GGATAGCAAGACTCTGACAAAG (SEQ. ID. NO. 7)). Subsequently, the membrane was washed and exposed to a film.
  • the vectors of the XvirPSJL group which are embodiments of the viruses referred to herein as group I adenoviruses and which are exemplified by the vectors and adenoviruses, respectively, XvirPSJL1 and XvirPSJL2, are not only, like adenovirus dl520, capable of replicating in YB-1 nucleus-positive cells, in particular tumor cells, but also in tumor cells in which YB-1 is overexpressed and deregulated, respectively.
  • E1B55k and E4orf6 are expressed only in dl520 infected YB-1 nucleus-positive cells under the influence of the E1B promoter and the E4 promoter, respectively, the expression of E1B55k and E4orf6 in XvirPSJL occurs by means of the cytomegalovirus (cmw) promoter.
  • cmw cytomegalovirus
  • other promoters in particular tumor-specific, tissue-specific and organ-specific promoters and the natural E1A promoter, i.e. in particular the E1A promoter as present in Adenoviruses of the wildtype, in particular Ad5, may be used.
  • the adenoviral vectors of the XvirPSJL group as disclosed herein thus combine various elements and thus functions of the adenoviral vectors dl520, Xvir03 and AdYB-1 in a single vector. Similar to the vector dl520 the XvirPSJL viruses contain the E1A12S gene. This gene and the corresponding gene product, respectively, is responsible for the induction of the S phase of the infected cell and promotes viral replication and the effect of chemotherapeutics and irradiation.
  • the XvirPSJL viruses contain the expression cassette CMV-E4orf6/IRES/E1B55k, which is required for an efficient replication and indirectly or directly transports deregulated YB-1 into the nucleus which is preferably contained in tumor cells.
  • replication is possible only in cells, particularly tumor cells, where YB-1 is overexpressed or deregulated.
  • P53 is made subject to degradation by the E1B55k/E4orf6 complex.
  • the sequence coding for human transcription factor YB-1 is taken from the virus AdYB-1. The endogenous, i.e. the YB-1 already present in the cell amplifies viral replication.
  • E1A12S and YB-1 are controlled by the YB-1-dependent adenoviral E2-late promoter.
  • specific promoters may be used in an embodiment, in particular tumor-specific, tissue-specific or organ-specific promoters.
  • a further feature of these viruses is that the E4 region is deleted.
  • the vector contains restriction sites there by which, in case of the adenoviral vectors XvirPSJL1 and XvirPSJL2, various transgenes as disclosed in the specification such as ribozymes, antisense molecules, siRNA, apoptosis-inducing genes, cytokines and prodrug genes may be expressed.
  • Their expression may also be controlled by tumor-specific, tissue-specific or organ-specific promoters as disclosed in the specification.
  • the localisation of the expression cassettes is not fixed, particularly not with regard to or within the E1, E3 and E4 region, but can be arranged in any way.
  • the vectors replicate independent of the p53 or Rb status of the tumor cells.
  • FIGS. 27 and 28 The structural designs of the recombinant adenoviruses XvirPSJL1 and XvirPSJL2 are presented in FIGS. 27 and 28 :
  • the pAdenoX plasmid of Clontech/BD Biosciences which is used as a starting material herein, comprises the genomic nucleic acid of adenovirus Ad5 and has a SfuI restriction site behind the 3′ ITR region which is ABSENT in wildtype adenovirus.
  • the E3-E4 region was transferred by SpeI (position 23644) and SfuI from pAdenoX (Clontech) into pcDNA3.1(+) (Invitrogen) and referred to as pcDNA3.1-E3 ⁇ 27865-30995-E4.
  • the majority of the E4ORF6, namely the bases 33241-33875 were removed by means of PstI.
  • the such obtained fragment was referred to as pcDNA3.1-E3 ⁇ 27865-30995, E4 ⁇ 33241-33875.
  • the E2-late promoter was excised from pGL3-EGFP (Holm et al., JBC 2002, 277, 10427-10434) with SacI and NheI and cloned into pcDNA3.1-E3 ⁇ 27865-30995, E4 ⁇ 33241-33875. In doing so, the E3 region was further deleted in the region of bases ⁇ 27593-31509. The thus obtained fragment was referred to as E2-late-pcDNA3.1-E3 ⁇ 27593-31509, E4 ⁇ 33241-33875
  • the cDNA for the E1A-243AA product was generated by means of RT-PCR, isolated and the sequence checked and cloned into the pcDNA3.1(+) vector (Invitrogen) using BamHI and EcoRI.
  • E1A-12S-pcDNA3.1+ was linearised with NheI and BamHI, made blunt-ended by T4 polymerase and provided with T overhangs by Taq polymerase and dTTPs.
  • the YB-1-EcoRI fragment was isolated from the vector pHVad2c (Holm et al., JBC 2002, 277, 10427-10434) and made blunt-ended.
  • the vector pShuttle (commercially available from BD Biosciences) was linearised with XbaI, the ends made blunt-ended and dephosphorylated and ligated with the previously produced YB-1 coding nucleic acid.
  • the vector thus obtained was referred to as YB-1-pShuttle.
  • the cloning into the pShuttle vector provided the YB-1 fragment coding nucleic acid with an in-frame STOP codon.
  • the YB-1 coding nucleic acid was cloned from the YB-1-pShuttle by means of NheI and BfrI into the vector IRES-E1A-12S in pcDNA3.1 (+). The thus obtained fragment was referred to as YB-1 (EcoRI-EcoRI with STOP codon)-IRES-E1A-12S-pcDNA3.1(+).
  • cassette YB-1-IRES-E1A12S was excised with PmeI and cloned into the NheI linearised, blunt-ended and dephosphorylated vector E2late-pcDNA3.1 E3 ⁇ 27593-31509, E4 ⁇ 33241-33875.
  • the second cassette is in the deleted region of the E3 region.
  • the cassette CMV-E1B55k/IRES/E4orf6 was excised by means of I-CeuI and PI-SceI from the pShuttle described above in relation to Xvir03 and inserted into the vector AdenoX/E2late-YB-1-IRES-E1A12S/E3 ⁇ 27593-31509, E4 ⁇ 33241-33875.
  • the vector was linearised with Pac I, transfected into 293 cells and the recombinant adenovirus XvirPSJL 1 and XvirPSJL 2, respectively, isolated without the transgenes indicated in the figure in accordance with manufacturer's instructions.
  • adenoviruses in accordance with the present invention, preferably recombinant adenovirus and in particular those containing, separately and/or together, the cassettes E4orf6-IRES-E1B55k and E1A12S-IRES-YB-1, respectively.
  • the individual transgenes can be exchanged within the individual cassettes and in particular among the respective cassettes.
  • the cassette E1A12S-IRES-YB-1 may consist only of E1A12S and/or E1A12S can be linked to other relevant genes through IRES.
  • the E2-late promoter was cloned into the HindIII and BglII cleavage site of the pGL3-enhancer plasmid (pGL3-E2-late) as paired oligonucleotides (upper primer 5′-TCGAGCTCCGCATTTGGCGGGCGGGATTGGTCTTCGTAGAACCTAATCTCGTGGGCGTGGTAGTCCTCAGGTACAAAT-3′ and lower primer 5′-AGCTTATTTGTACCTGAGGACTACCACGCCCACGAGATTAGGTTCTACGAAGACCAATCCCGCCCGCCAAATGCGGAGC-3′).
  • the luciferase gene was excised using NcoI and XbaI, the ends made blunt ended and T-ends added.
  • the transgene E1A 12S which was amplified by the primers E1A 12S forward primer 5′-ATGGCCGCCAGTCTTTTG-3′ and E1A 12S backward primer 5′-TTATGGCCTGGGGCGTTTAC-3′, was introduced by TA-cloning into the thus opened site.
  • This cassette was excised using PvuI and ClaI, the ends made blunt ended and cloned into the blunt ended and dephosphorylated NheI-cleavage site in the E3-region of E3E4-pShuttle (-NdeI)-AdEASY.
  • the cassette thus contains the E2-late promoter, the open reading frame E1a-12S and the SV-40 late polyadenylation signal.
  • the resulting construct is E2-late-E1a-12S-E3E4-pShuttle(-NdeI)-AdEASY.
  • E2-late-E1a 12S-E3E4 was excised from the E2-late-E1a 12S-E3E4-pShuttle (-NdeI)-AdEASY using SpeI and PacI and cloned into the SpeI and PacI cut pAdEASY.
  • the thus resulting construct was referred to as E2-late-E1a 12S-E3E4-pAdEASY.
  • AdPSJL-12S-AdEASY was generated by homologous recombination upon transforming BJ5183 (EC) bacteria with the plasmids Xvir-3′UTR in pShuttle AdEASY and E2-late-E1a 12S-E3E4-pAdEASY.
  • E1a 12S The amplificates E1a 12S (see above) and the IRES element (see above) were subsequently cloned into the multiple cloning site of the pcDNA3.1(+)-vector.
  • the E1a-12S amplificate was introduced into the blunt ended BamHI-cleavage site by TA-cloning.
  • the plasmid E1a-12S in pcDNA3.1(+) was linearized with EcoRV, T-ends added and the amplificate cloned into the IRES element.
  • the thus obtained plasmid was subsequently linearized with XhoI, the ends made blunt ended and the EcoRI-EcoRI-cleavage product of YB-1 which is devoid of a stop codon.
  • E1A-12S-IRES-pcDNA3.1(+) was linearized using NotI and the ends made blunt ended. Also, the YB-1-EcoRI-cleavage product was made blunt ended and introduced into the dephosphorylated vector E1A-12S-IRES-pcDNA3.1(+).
  • the cassette E1A-12S-IRES-YB-1 was removed using PmeI and cloned into the above described plasmid pGL3-E2-late after removal of the luciferase gene with NcoI and XbaI and blunt ending and dephosphorylation.
  • the cassette E2-late-E1A-12S-IRES-YB-1 was excised using PvuI and ClaI, the ends made blunt ended and cloned into the blunt ended and dephosphorylated NheI-cleavage site in the E3-region of E3E4-pShuttle (-NdeI)-AdEASY.
  • the thus obtained construct is E2-late promoter-E1A-12S-IRES-YB-1-E3E4-pShuttle (-NdeI)-AdEASY.
  • E2-late promoter-E1A-12S-IRES-YB-1-E3E4 cassette was excised from the E2-late promoter-E1A-12S-IRES-YB-1-E3E4-pShuttle (-NdeI)-AdEASY with SpeI and Pad and cloned into the SpeI and Pad cut pAdEASY.
  • the resulting construct was referred to as E1a-12S-IRES-YB-1-E3E4-pAdEASY.
  • AdPSJL-12S-Yb-1-AdEASY was generated by homologous recombination upon transformation of B15183 (EC) bacteria with the plasmid Xvir-3′UTR in pShuttle AdEASY and E1a-12S-IRES-YB-1-E3E4-pAdEASY.
  • E2-late promoter-E1A-12S and/or E2-late promoter-E1A-12S-IRES-YB-1 can be introduced into the E4-region. Alternatively, the E2-region may remain intact under such conditions.
  • the HI loop of the fibre knob domain was modified according to Dmitriev et al. 1998 (An Adenovirus Vector with Genetically Modified Fibers Demonstrates Expanded Tropism via Utilization of a Coxsackievirus and Adenovirus Receptor-Independent Cell Entry Mechanism): The respective region was amplified using the primes RGD-Hpa fw (5′-GAGgttaacCTAAGCACTGCCAAG-3′), RGD-EcoRV rev (5′-CATAGAGTATGCAGATATCGTTAGTGTTACAGGTTTAGTTTTG-3′), as well as RGD-EcoRV fw (5′-GTAACACTAACGATATCTGCATACTCTATGTCATTTTCATGG-3′) and RGD-Bfr rev (5′-CAGCGACATGAActtaagTGAGCTGC-3′) and an EcoRV-cleavage site thus generated.
  • RGD-Hpa fw 5′-GAGgttaacCT
  • RGD Arg-Gly-Asp
  • HeLa cells were plated per dish. At the next day the cells were infected with various titers (pfu/ml) of adenovirus dl520. The infection was done in 500 ⁇ l serum-free DMEM medium for 1 h at 37° C. Subsequently, the infection medium was removed and replaced by 2 ml complete medium (10% FCS/DMEM). After 3-5 days an analysis was performed using crystal violet staining.
  • the result of this experiment is depicted in FIG. 23 .
  • the adenovirus dl520 does not show any lysis at low MOIs (5-10 pfu/cell) upon infection of HeLa cells which do not have YB-1 in the nucleus.
  • dl520 showed a factually complete lysis at an MOI (multiplicity of infection) of 100-200 pfu per cell and a still predominant lysis at an MOI of 50 pfu per cell.
  • dl520 and similar viruses which are capable of switching on the adenoviral genes E1B55k and E4orf6 at higher MOIs, are suitable to transport either directly or indirectly overexpressed or deregulated YB-1 into the nucleus and thus to induce cell lysis.
  • YB-1 binds to the adenoviral E2-late promoter in the nucleus (Holm et al., JBC 2002, 277, 10427-20434) and that this promoter is also well suited for the expression of nucleic acids.
  • the use of the adenoviral E2-late promoter is particularly motivated by the fact that it can be regulated by YB-1, whereby YB-1 acts as a positive effector, i.e. the promoter is only active in the presence of YB-1 in the nucleus.
  • adenoviral E2-late promoter can be regulated in a highly selective manner and thus used in systems in which YB-1 is present in the nucleus and factually avoids any expression of the nucleic acid which is under the control of the adenoviral E2-late promoter in case that YB-1 is not present in the nucleus as an effector and regulator, respectively.
  • the E2-late promoter comprises 3 Y-boxes (CCAAT) which are relevant for the activation of the E2 gene.
  • CCAAT Y-boxes
  • EPG-257 RDB epidermal stomach carcinoma
  • HeLa epidermal uterine cervix carcinoma
  • U2OS osteosarcoma
  • the cells were processed with the Luciferase Assay System Kit of Promega (Cat. No. E1500) 48 h after infection: Each well was provided with a layer of 500 ⁇ l lysis buffer, the cells rinsed off from the well plate with a 1 ml pipette after 10 minutes at room temperature and transferred into a 1.5 ml locking cap reaction vessel. The cell lysate was subsequently centrifuged at 4° C. for 15 minutes at 14.000 rpm.
  • the following plasmids were used: pGL3-enhancer (Promega) from which the enhancer was removed by means of BamHI (2250 bp) and BsaBI (2003 bp), served as a blank reading.
  • the various E2 promoter constructions were cloned into the MCS in the enhancer-lacking pGL3 vector by means of restriction sites Apa I and Sac I.
  • the hCMV promoter was cloned by means of Bgl II and Hind III into the pGL3 enhancer and served as a positive control.
  • the positive control allowed to estimate transfection efficiency and also served as a reference value for luciferase activity.
  • the CMV control was set 100% and the enzyme activity produced by the E2 promoter constructions put in relation thereto and depicted as a bar graph in FIG. 24 .
  • the results presented in FIG. 30 confirm in an impressive manner that the individual promoter fragments which contain different E2-late/Y-boxes, are suitable for the expression of therapeutic transgenes in YB-1 nucleus-positive tumor cells and may thus be used as promoters in the meaning of the present invention.
  • the result depicted in FIG. 31 confirms that AdYB-1, as a whole, produces more pfu than Ad312 and releases more particles. After 5 days the AdYB-1 infected cells clearly show a cytopathic effect (CPE) in contrast to Ad312-infected cells.
  • CPE cytopathic effect
  • FIG. 32 shows a schematic representation of the regulation of the E2 region of adenovirus by the E2-late and E2-early promoters through E2F and YB-1.
  • the involved promoters E2-early and E2-late promoter
  • FIG. 1 the involved promoters, E2-early and E2-late promoter, are depicted with regard to the binding and activation, respectively, by E2F and 113-1.
  • the wildtype E1A protein interferes with the binding of E2F to the retinoblastoma protein Rb.
  • the thus released E2F binds to the E2-early promoter and induces thereby adenoviral replication.
  • 8-12 h a so-called switch to the E2-late promoter occurs. This is only enabled upon the translocation of YB-1 from the cytoplasm into the nucleus.
  • nuclear localisation YB-1 activates E2 gene expression by binding to the E2-late promoter.
  • E2F/RB and the E1A mediated release of E2F is fundamentally different from the mechanism underlying the present invention.
  • the release of E2F from the Rb protein as assumed in the prior art, is not an important, not to say a non-critical process of adenoviral replication, but the nuclear localisation of the human transcription factor YB-1 is the critical factor therefor. This transcription factor is present in normal cells only in the cytoplasm over the bigger part of the cell cycle.
  • tumor diseases including but not limited to breast cancer, ovarian cancer, prostate cancer, osteosarcoma, glioblastoma, melanoma, small-cell lung cancer and colorectal cancer.
  • the promoter is additionally E1B 19K-minus and protein DC-minus in the sense that protein IX is not contained in the regulatory context as present in the wildtype and protein IX is not expressed. Rather, the expression is controlled by the E2-late promoter.
  • the protein IX has been cloned into the E3 region, however, can, in principle, also be cloned into the E4 region.
  • the genes for E2A, E2B, E4 and MLP are still present and may also be expressed.
  • the transporter consisting of E4orf6 and E1B55K is formed by the cassette E4orf6-IRES-E1B55K which is under the control of the CMV promoter.
  • the respective cassette has been cloned into the E1 region, however, could also be cloned into other regions such as, for example, the E3 and E4 region.
  • the adenovirus is additionally E1B19K-minus and protein DC-minus in the sense that protein DC is not contained in the regulatory context as in wildtype and protein IX is not expressed. Rather the expression is caused by the E1A12S which is controlled by the E2-late promoter which results in activating the open reading frame for protein IX which is present in the region coding for E1B55K.
  • the protein E1A12S is cloned into the E3 region, however, can, in principle, also be cloned into the E4 region.
  • the genes for E2A, E2B, E4 and MLP are still present and can also be expressed.
  • the transporter consisting of E4orf6 and E1B55K is formed by the cassette E4orf6-IRES-E1B55K which is under the control of the CMV promoter.
  • the respective cassette has been cloned into the region of the E1 region, however, could also be cloned into different regions such as, e.g., the E3 or E4 region.
  • the adenovirus is additionally E1B19K-minus and protein IX-minus in the sense that protein IX is not present in the regulatory context as present in wildtype. Rather the expression is controlled by the protein E1B19K which is expressed under the influence of the CMV promoter and allows that the reading frame of protein IX is expressed which is contained in the E1B55K reading frame.
  • the genes for E2A, E2B, E3, E4 and MLP are still present and may also be expressed.
  • the transporter consisting of E4orf6 and E1B55K is formed by the cassette E4orf6-RSV promoter E1B region which is controlled by the CMV promoter.
  • the respective cassette has been cloned into the E1 region, however, could also be cloned into different regions such as, e.g., the E3 or E4 region.
  • the adenovirus is additionally E1B19K-minus and protein DC-minus in the sense that protein E1B19K is not present in the regulatory context as present in the wildtype adenovirus and protein IX is not expressed. Rather, the expression is controlled by the natural E3 promoter.
  • the genes for E2A, E2B, E4 and MLP are still present and may also be expressed.
  • the transporter consisting of E4orf6 and E1B55K is formed by the cassette E4orf6-IRES-E1B55K which is under the control of the CMV promoter.
  • the respective cassette has been cloned into the E1 region, however, could also be cloned into different regions such as, e.g., the E3 or E4 region.
  • FIGS. 38-41 present further embodiments of the adenoviruses in accordance with the present invention.
  • the virus depicted in FIG. 38 is a further development of the adenovirus Xvir 05/E1B19K as depicted in FIG. 36 .
  • this virus exhibits a cassette which is under the control of the E2-late promoter, comprising E1A12S and YB-1 and a nucleic acid coding therefor, respectively, whereby both reading frames are separated by an IRES.
  • the nucleic acid coding for YB-1 is not contained in the cassette.
  • the nucleic acid for YB-1 which is expressed by the virus results in an even more pronounced replication in cells having deregulated YB-1.
  • the adenovirus depicted in FIG. 40 is a further development of the adenovirus depicted in FIG. 35 , whereby the cassette which is under the control of the E2-late promoter, comprises E1A12S and YB-1 and nucleic acids each coding therefor, respectively, and is cloned into the E4 region and several transgenes are cloned into the E3 region under the control of the E3 promoter such as, e.g., apoptosis-inducing genes, prodrug genes, siRNA, tumor suppressor genes or cytokines.
  • the various transgenes disclosed herein may be cloned into this region.
  • the adenovirus in accordance with the present invention depicted in FIG. 41 is finally a further development of the adenovirus depicted in FIG. 40 , whereby in connection therewith the RGD motif has been introduced by cloning which is advantageous for the targeting of the viruses. It is present in the adenoviral genome in the fibre protein approximately in the range of positions 32576-32685. This variation of the precise positioning is caused by the fact that the sequence of wildtype adenoviruses are different in the various data banks and data bank entries and have different lengths, respectively.
  • the adenovirus in accordance with the present invention and depicted in FIG. 39 is based on the adenovirus presented in FIG. 36 .
  • this adenovirus does not comprise a cassette consisting of E4orf6 and E1B55K, but both are controlled by different promoters, namely the CMV promoter and the RSV promoter. The cloning has been done into the E1 region.
  • the adenovirus comprises apart from the nucleic acid coding for E1A12S which is under the control of the E2-late promoter, still a further nucleic acid coding for protein IX, which is separated from the one coding for E1A12S by an IRES.
  • this cassette could, in principle, also lack a nucleic acid coding for protein IX.
  • a further possible embodiment could be such that the cassette is cloned into the E4 region.
  • this virus could still contain in the E3 or E4 region the transgenes as described in connection with the virus depicted in FIG. 8 . In a further embodiment of these viruses, the RGD motif is contained.
  • the experiment was performed as follows: For each 10 cm dish 10 6 293 and 257 RDB cells were plated. The next day the cells were, as depicted in FIG. 10 , either not infected (K), infected with wildtype adenovirus or with Xvir03. The infection occurred in 1.5 ml serum-free DMEM medium for 1 h at 37° C. Subsequently, the infection medium was removed and replaced by 10 ml complete medium (10% FKS/DMEM). After 24-48 h the RNA was isolated. Subsequently, a Northern blot analysis was performed.
  • RNA were separated electrophoretically in an agarose gel with 3% formaldehyde, subsequently blotted onto a nylon membrane and hybridised against a specific 386 bp probe.
  • a P32 labelled probe directed against protein IX was used as a probe and generated using PCR.
  • the following primers were used for the PCR: 5′-TATTTGACAACGCG; 5′-TTTTAAACCGCATTGGG.
  • the position of the probe in wildtype adenovirus genome is between position 3648 and 4033.
  • the virus which is used, is Xvir 03 which does not expression of protein IX.
  • the virus Xvir03-3′UTR shows a decreased expression in tumor cells 257RDB compared to wildtype adenovirus.
  • 293 cells which express E1A and MB proteins, among others also the E1B19K protein sufficient protein IX is expressed.
  • a P32 labelled probe targeting the protein IX was used as a probe and generated by means of PCR.
  • the following primers were used for the PCR: 5′-TATTTGACAACGCG; 5′-TTTTAAACCGCATTGGG.
  • the position of the probe in the wildtype adenovirus genome is between position 3468 and 4033.
  • the result shows that adenovirus Xvir03 does not recombine after infection of 293 cells.
  • the sizes of the cleavage products are represented in the figure.
  • Per 10 cm dish 10 6 257RDB cells were plated. The next day the cells were infected with the various adenoviruses as depicted in FIG. 45 . The infection was performed in 1.5 ml serum-free DMEM medium for 1 h at 37° C. Subsequently, the infection medium was removed and replaced by 10 ml complete medium (10% FKS/DMEM). After 3-4 days the RNA was isolated. Subsequently, a Northern blot analysis was performed.
  • RNA were electrophoretically separated in an agarose gel containing 3% formaldehyde, subsequently blotted onto a nylon membrane and hybridised against a specific P32 labelled MDR probe (Holm et al., British J. Cancer, 1994, 70, 239-243).
  • P32 labelled MDR probe Holm et al., British J. Cancer, 1994, 70, 239-243.
  • DU145 cells were plated per 10 cm dish. The next day the cells were infected with the various adenoviruses as depicted in FIG. 46 . The infection was performed in 1.5 ml serum-free DMEM medium for 1 h at 37° C. Subsequently, the infection medium was removed and replaced by 10 ml complete medium (10% FKS/DMEM). After 3-4 days the RNA was isolated. Subsequently, a Northern blot analysis was performed. For such purpose each 10 ⁇ g RNA were electrophoretically separated in an agarose gel containing 3% formaldehyde, subsequently blotted onto a nylon membrane and hybridised against a specific P32 labelled MRP probe. The result shows that the adenovirus Xvir03 is capable of inhibiting the expression of the ABC transporter MRP.
  • the recombinant adenovirus Xvir03 is capable of inhibiting the expression of the resistance relevant genes MRP and MDR1.
  • MRP and MDR1 This is perfected by the complex consisting of E4orf6 and E1B55k recruiting the human cellular transcription factor YB-1 for adenoviral replication.
  • this transcription factor which is otherwise involved in the expression of the genes MDR1 and MRP, is no longer available for their expression. Consequently, the expression of MRP and MDR1 proteins is reduced after infection with Xvir03. This results in a sensitisation of tumor cells against various cytostatics, e.g. daunorubicin ( FIG. 9 ).
  • Per dish 100,000 DU145 and PC3 cells were plated. The next day the cells were infected with different concentrations of Xvir03 (PFU/cell) as depicted in FIGS. 47 and 48 . The infection was performed in 500 ⁇ l serum-free DMEM medium for 1 h at 37° C. Subsequently, the infection medium was removed and replaced by 2 ml complete medium (10% FKS/DMEM). After 5-7 days the evaluation was performed using crystal violet staining. For such purpose, first the medium is removed. Subsequently, the cells are overlayed with crystal violet (50% ETOH, 3% formaldehyde, 5% acetic acid, 1% crystal violet) and incubated at room temperature for 5-15 min. Subsequently, the plates are thoroughly rinsed with water and dried at room temperature.
  • crystal violet 50% ETOH, 3% formaldehyde, 5% acetic acid, 1% crystal violet
  • the results of the experiment are depicted in FIGS. 47 and 48 .
  • the adenovirus Xvir03 is capable of lysing tumor cells at an MOI of about 30-50.
  • the infection of tumor cells by Xvir03 results in a more pronounced inhibitory effect of daunorubicin in combination with Xvir03 on tumor cell growth compared to daunorubicin alone.
  • the expression of the viral proteins E4orf6 and E1B55k, among others, is ensured in vector Xvir05 by the expression cassettes CMV-E4orf6 and RSV-E1B region. This results in a translocation of YB-1 into the nucleus.
  • the E1A12S gene product as well as the YB-1 gene product controlled by the E2-late promoter additionally promote viral replication. Additionally, the virus is capable of inhibiting the expression of the ABC transporter MRP and MDR1. Additionally, the proteins E1B19K and protein IX are expressed as constituents of the cassette RSV-E1B region.
  • the vector Xvir05 protein IX is a further development of the vector. There, the expression of the adenoviral protein IX is ensured by the expression cassette E2late-E1A12S-IRES-protein IX.
  • the vector does not comprise the complete E1B region but only the open reading frame of E1B55k.
  • the complete E1B region i.e. the E1B19k, E1B55k and the protein IX are controlled by a viral, non-adenoviral promoter such as, for example, the RSV promoter.
  • the expression cassette E2late-E1A12S-IRES-YB-1 is present in the E4 region.
  • specific therapeutic transgenes may be cloned into the E3 region.
  • the E3 deletion is such that the adenoviral ADP protein “adenoviral death protein”, is still expressed.
  • the expression of E1A12S and E1B19k effect the expression of protein DC.
  • the vector Xvir05/02 additionally comprises an RGD motif in the H loop of the fibre knob in order to increase a better infection rate.
  • the generation of the viruses was performed as follows:
  • cassette CMV-MCS-polyA was cut out of the pShuttle from Clontech using MfeI and EcoRI, the ends made blunt-ended and cloned into the vector pShuttle (-EcoRI)-AdEASY, which has been linearised using XbaI for such purpose, made blunt-ended and dephosphorylated. Plasmid CMV-MCS-PolyA-pShuttle-AdEASY was created therefrom.
  • the ⁇ E3E4 region of plasmid pAdEASY was cloned with SpeI and Pad into plasmid CMV-MCS-PolyA-pShuttle-AdEASY and thus the plasmid ⁇ E3E4-pShuttle-AdEASY generated.
  • restriction with NdeI and religation one of the two NdeI restriction sites was deleted and thus also a multiple cloning site from the plasmid.
  • plasmid ⁇ E3E4-pShuttle (-NdeI)-AdEASY was generated.
  • the E4 region in plasmid ⁇ E3E4-pShuttle (-NdeI)-AdEASY was specifically deleted.
  • Respective deletions may be performed in different systems for the generation of recombinant adenoviruses by the one skilled in the art.
  • the HI loop of the fibre knob domain was modified in accordance with Dmitriev et al. 1998 (An Adenovirus Vector with Genetically Modified Fibers Demonstrates Expanded Tropism via Utilization of a Coxsackievirus and Adenovirus Receptor-Independent Cell Entry Mechanism): The respective region was amplified using the primers RGD-Hpa fw (5′-GAGgttaacCTAAGCACTGCCAAG-3′), RGD-EcoRV rev (5′-CATAGAGTATGCAGATATCGTTAGTGTTACAGGTTTAGTTTTG-3′) as well as RGD-EcoRV fw (5′-GTAACACTAACGATATCTGCATACTCTATGTCATTTTCATGG-3′) and RGD-BfrI rev (5′-CAGCGACATGAActtaagTGAGCTGC-3′) and thereby an EcoRV-cleavage site generated.
  • RGD-Oligo 1 (5′-CACACTAAACGGTACACAGGAAACAGGAGACACAACTTGTGACTGCCGCGGAGACTGTTTCTGCCC-3′) and RGD-Oligo 2 (5′-GGGCAGAAACAGTCTCCGCGGCAGTCACAAGTTGTGTCTCCTGTTTCCTGTGTACCGTTTAGTG-3′).
  • the 2709 bp fragment was cloned which was excised with SpeI (27083 bp) and XhoI (29792 bp) from wildtype virus DNA (pcDNA3.1(+) oCMV/E3aXhoI).
  • HpaI (30570 bp) rather than XhoI at the 3′ end.
  • the vector pcDNA3.1(+) oCMV is then cleaved with SpeI and EcoRV and the adenoviral SpeI-HpaI fragment is cloned therein (pcDNA3.1(+) oCMV/E3aHpaI).
  • pcDNA3.1(+) oCMV/E3aHpaI adenoviral SpeI-HpaI fragment is cloned therein
  • a further option is the 2718 bp EcoRI fragment of adenovirus wildtype DNA (positions 27332 bp and 30050 bp) which is cloned into the pcDNA3.1(+) oCMV which has been opened using EcoRI (pcDNA3.1(+) oCMV/E3aEcoRI).
  • the plasmid was cleaved with XhoI, the ends made blunt-ended and further cleaved with SpeI. The fragment thus cut out was cloned into the previously cut plasmid ⁇ E3RGD-E4 ⁇ ORF6-pShuttle (-NdeI)-AdEASY.
  • the fragments SpeI-HpaI (position 27083 bp to 30570 bp) and EcoRI (position 27332 bp to 30050 bp) may be excised the same way from the respective pcDNA3.1(+) oCMV/E3a constructs and transferred by cloning.
  • the E3a region may be amplified by PCR using the primers E3a forward (SpeI) 5′-CTTAAGGACTAGTTTCGCGC-3′ and E3a reverse (XhoI, NheI) 5′-CAAGCTAGCTCGAGGAATCATG-3′ with the adenovirus type 5 wildtype DNA as template.
  • E3a reverse primer an NheI cleavage site is generated.
  • the amplificate is restricted with SpeI and NheI and cloned into the similarly SpeI and NheI cleaved vector ⁇ E3RGD-E4 ⁇ ORF6-pShuttle (-NdeI)-AdEASY.
  • the E3a region can be amplified using the primers E3a forward (SpeI) 5′-CTTAAGGACTAGTTTCGCGC-3′ and E3a reverse (HpaI, NheI) 5′-CACGCTAGCAAGTTAACCATGTCTTGG-3′ using adenovirus type 5 wildtype DNA as template.
  • E3a reverse primer an NheI cleavage site is generated.
  • the amplificate is restricted with SpeI and NheI and is cloned into the vector ⁇ E3RGD-E4 ⁇ ORF6-pShuttle (-NdeI)-AdEASY which is also cleaved by SpeI and NheI.
  • the E3a region can be amplified by PCR using the primers E3a forward (EcoRI) 5′-GAAACCGAATTCTCTTGGAAC-3′ and E3a reverse (NheI, EcoRI) 5′-GAATTCTAGCTAGCTCAGCTATAG-3′ with adenovirus type 5 wildtype DNA as template.
  • E3a reverse primer an NheI cleavage site is generated.
  • the amplificate is restricted with EcoRI and NheI and cloned into the vector ⁇ E3RGD-E4 ⁇ ORF6-p Shuttle (-NdeI)-AdEASY which is also cleaved by EcoRI and NheI.
  • the thus cloned region comprises the E3 region until the open reading frame for the E3 ADP (position 29772 bp) and thus the E3 promoter, the complete E3A region with polyadenylation signal, the transcription start and the open reading frame for 12.5 K, E3 6.7 K, E3 gp19 K and E3 ADP.
  • E3 promoter and the open reading frame for the ADP in plasmid pcDNA3.1(+) oCMV/E3a:
  • positions 27596 bp and 29355 bp for example with EcoRII, BsiWI, DraI, MunI
  • the open reading frames for 6.7 K and gp19 K positioned in between may be removed and thus provided 1.8 kb more space for incorporating further transgenes.
  • the above mentioned E3a amplificates can also be truncated by a corresponding restriction and as previously described transferred by cloning.
  • E2Late promoter was cloned as paired oligonucleotide (Upper Primer 5′-TCGAGCTCCGCATTTGGCGGGCGGGATTGGTCTTCGTAGAACCTAATCTCGTGGGCGTGGTAGTCCTCAGGTACAAAT-3′ and Lower Primer 5′-AGCTTATTTGTACCTGAGGACTACCACGCCCACGAGATTAGGTTCTACGAAGACCAATCCCGCCCGCCAAATGCGGAGC-3′ into the HindIII and BglII cleavage site of the pGL3 enhancer plasmid of the company Promega (pGL3-E2Late).
  • the luciferase gene was excised with NcoI and XbaI, the ends made blunt-ended and T ends added.
  • the transgene E1A12S which was amplified by RT-PCR using the primers E1a 12S forward 5′-ATGGCCGCCAGTCTTTTG-3′ and E1a 12S reverse 5′-TTATGGCCTGGGGCGTTTAC-3′, was introduced by TA cloning.
  • the cassette thus contains the E2Late promoter, the open reading frame E1a-12S and the SV-40 Late polyadenylation signal of the vector pGL3.
  • This cassette was excised with PvuI and ClaI, the ends made blunt-ended and can now be cloned optionally into the EcoRII, BsiWI, DraI, MunI deleted E3a region (after removal of the open reading frames for E3 6.7 K and gp19 K, see above) or in the deletion of E4ORF6 cloned, for example into the blunt-ended and dephosphorylated BfrI cleavage site.
  • the resulting construct is E3a/E2Late-E1a-12S/ ⁇ E3RGD-E4 ⁇ ORF6-pShuttle (-NdeI)-AdEASY or E3a ⁇ E3RGD-E4 ⁇ ORF6/E2Late-E1a-12S-pShuttle (-NdeI)-AdEASY.
  • the E1a-12S amplificate was introduced into the blunt-ended BamHI restriction site through TA cloning.
  • E1a-12S in pcDNA3.1(+) was linearised with EcoRV, the T ends added and the amplificate for the IRES element cloned.
  • the thus generated construct E1a-12S-IRES-pcDNA3.1(+) was linearised using NotI and the ends blunt-ended, also the YB-1 EcoRI cleavage product of plasmid pHVad2c CMV/S40+Yb-1 s (Stephan Bergmann) blunt-ended and introduced into the dephosphorylated vector E1A-12S-IRES-pcDNA3.1(+).
  • the PCR amplificate for the open reading frame of protein IX can be introduced into the blunt-ended Nod cleavage site of the vector E1a-12S-IRES-pcDNA3.1(+) after adding T ends, specifically with the primers IX forward 5′-ATGAGCACCAACTCGTTTG-3′ and IX reverse 5′-GTTTTAAACCGCATTGGGAGG-3′.
  • E1A-12S-IRES-YB-1 or E1A-12S-IRES protein IX were excised with PmeI and cloned into the above described plasmid pGL3-E2Late after removal of the luciferase gene with NcoI and XbaI and blunt-ending and dephosphorylation.
  • This cassette E2late-E1A-12S-IRES-YB-1 was excised with PvuI and ClaI, the ends blunt-ended and can now optionally be cloned into the EcoRII, BsiWI, DraI, MunI deleted E3a region (after removal of the open reading frames for E3 6.7 K and gp19 K, see above) or in deletion of the E4ORF6, for example in the blunt-ended and dephosphorylated BfrI cleavage site.
  • the resulting construct is E3a/E2Late-E1a-12S-IRES-YB-1/ ⁇ E3RGD-E4 ⁇ ORF6-pShuttle (-NdeI)-AdEASY or E3a ⁇ E3RGD-E4 ⁇ ORF6/E2Late-E1a-12S-IRES-YB-1-pShuttle (-NdeI)-AdEASY.
  • E3a ⁇ E3RGD-E4 ⁇ ORF6 region with the second expression cassette E2Late-E1a-12S or E2Late-E1a-12S-IRES-YB-1 in E3a or E4 ⁇ ORF6 were excised using SpeI and PacI from the corresponding pShuttle plasmid E3a ⁇ E3RGD-E4 ⁇ ORF6-pShuttle (-NdeI)-AdEASY and cloned into the accordingly opened vector pAdEASY, whereby the new rescue vector E3a/E2Late-E1a-12S/ ⁇ E3RGD-E4 ⁇ ORF6-pAdEASY or E3a ⁇ E3RGD-E4 ⁇ ORF6/E2Late-E1a-12S-pAdEASY and E3a/E2Late-E1a-12S-IRES-YB-1/ ⁇ E3RGD-E4 ⁇ ORF6-pAdEASY, respectively, or E
  • E3a ⁇ E3RGD-E4 ⁇ ORF6-pAdEASY contains the E3a region, an RGD motif and a deleted E4ORF6, as a second expression cassette either the E2Late-E1a-12S or the E2Late-E1a-12S-IRES-YB-1 are present in E3a or E4 ⁇ ORF6.
  • This construct is the rescue plasmid for introducing further transgenes into the E1 region through a shuttle plasmid.
  • the adenogenome was restricted with XbaI (position 1340 bp) and MunI (position 3925 bp) for the MB region and the 2585 bp fragment cloned into the pShuttle of AdEASY into the XbaI and MunI cleavage sites which thus contains the complete E1B region (pShuttle/E1B).
  • the E1B region can be amplified by PCR using the primers E1B forward 5′-GTGTCTAGAGAATGCAATAGTAG-3′ and E1B reverse 5′-GTCAAAGAATCCAATTGTGC-3′ using the adenovirus type 5 wildtype DNA as template, can be restricted with XbaI and MunI and cloned into the XbaI and MunI restriction sites of the pShuttle of AdEASY.
  • the pShuttle/E1B comprises the MB promoter, the open reading frames for E1B19K, E1B55K and the protein DC and the natural poly-A portion.
  • the E1B promoter was removed using XbaI and HpaI, the ends of the vectors blunt-ended and replaced by the CMV promoter from the pcDNA3.1(+) of the company Invitrogen, which was cut with MluI and XhoI and the ends of which have also been blunt-ended.
  • an RSV promoter used instead of the CMV promoter or a tumor specific and viral promoter, respectively, can control the expression of the E1B region, for example the promoters recited in the patent.
  • the plasmid pRc/RSV of the company Invitrogen was cleaved with XhoI, SpeI and XbaI.
  • the thus generated 2810 bp and 278 bp fragments were again ligated so that the F1 origin and the neomycine resistance gene (oNeo) were removed.
  • the thus generated vector pRc/RSV contains one BamHI cleavage site only into which the open reading frame of E4ORF6 from the plasmid CGN from Dobbelstein was cloned.
  • the amplificate of a PCR using the primers E4ORF6-forward 5′-ATGACTACGTCCGGCGTTCC-3′ and E4ORF6-reverse 5′-CTACATGGGGGTAGAGTC-3′ can be introduced into the EcoRV cleavage site of the vector pRc/RSV (oNeo) after adding the T ends (TA cloning).
  • a CMV promoter (taken from pcDNA3.1(+) with MluI and HindIII) instead of the RSV promoter (by removal with MluI and HindIII) or a tumor-specific and viral promoters, respectively, direct the expression of the E4orf6, for example the promoters recited in the patent.
  • the cassette RSV-E4ORF6-polyA (the Bovine Growth Hormone polyadenylation signal is derived from plasmid pRC/RSV) was cleaved with MunI, the ends made blunt-ended and further retrieved from the plasmid with XhoI.
  • the expression cassette was subsequently cloned into the vector pShuttle/E1B which had been cleaved with NotI, made blunt-ended and subsequently cleaved with XhoI. By doing so, the vector RSV-E4ORF6-polyA/E1B-pShuttle-AdEASY was generated.
  • the vector RSV-E4ORF6-polyA/E1B-pShuttle-AdEASY for the E1 region was linearised using Bst1107I and MroI and introduced into B15183 (EC) bacteria together with the rescue plasmid (see above) by means of electroporation.
  • the adenoviral plasmid RSV-E4ORF6-polyA/E1B-E3a/E2Late-E1a-12S/ ⁇ E3RGD-E4 ⁇ ORF6-pAdEASY generated by homologous recombinant (or correspondingly with the other above recited rescue vector variants) which resulted in virus production after transfection in HEK293 cells.
  • adenoviruses in accordance with the present invention preferably recombinant adenoviruses, and in particular those which contain the above-mentioned expression cassettes either individually and/or together
  • other systems e.g. pAdenoX system of the company Clontech/BD Biosciences or the system of the company Microbix.

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180099014A1 (en) * 2016-10-07 2018-04-12 Miami University Engineered oncolytic viruses containing hyper-binding sites to sequester and suppress activity of oncogenic transcription factors as a novel treatment for human cancer
US11077156B2 (en) 2013-03-14 2021-08-03 Salk Institute For Biological Studies Oncolytic adenovirus compositions
US11130968B2 (en) 2016-02-23 2021-09-28 Salk Institute For Biological Studies High throughput assay for measuring adenovirus replication kinetics
US11401529B2 (en) 2016-02-23 2022-08-02 Salk Institute For Biological Studies Exogenous gene expression in recombinant adenovirus for minimal impact on viral kinetics
US11813337B2 (en) 2016-12-12 2023-11-14 Salk Institute For Biological Studies Tumor-targeting synthetic adenoviruses and uses thereof

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1506021B1 (de) 2002-05-27 2019-05-01 Per Sonne Holm Verwendung von adenoviren und dafur kodierenden nukleinsäuren
EP1689445B1 (de) 2003-11-14 2015-02-25 Per Sonne Holm Neue verwendung von adenoviren und dafür codierende nukleinsäuren
EP1830864A2 (de) * 2004-12-31 2007-09-12 Per Sonne Holm E1 -minus adenoviren und deren verwendung
WO2010068794A2 (en) * 2008-12-10 2010-06-17 The General Hospital Corporation Hif inhibitors and use thereof
WO2013119880A1 (en) * 2012-02-07 2013-08-15 Global Bio Therapeutics Usa, Inc. Compartmentalized method of nucleic acid delivery and compositions and uses thereof
US10202568B2 (en) 2013-08-12 2019-02-12 Invivosciences Inc. Automated cell culture system and method
CN110461323A (zh) 2017-03-31 2019-11-15 绪方久修 溶瘤病毒的增殖方法和抗肿瘤剂
EA201990822A1 (ru) 2017-04-12 2020-01-09 Эписентарикс, Инк. Иммуномодулирующие слитые белки
EP3630959A4 (en) * 2017-05-24 2021-03-17 EpicentRx, Inc. ANTI-ANGIOGENIC ADENOVIRUS
CN109576231B (zh) 2017-09-28 2022-03-25 北京康万达医药科技有限公司 分离的重组溶瘤腺病毒、药物组合物及其在治疗肿瘤和/或癌症的药物中的用途
CN113774031B (zh) * 2020-06-10 2024-04-02 广州恩宝生物医药科技有限公司 一种复制型人腺病毒及其应用
EP4410971A1 (en) * 2021-09-30 2024-08-07 FUJIFILM Corporation Method for producing adeno-associated virus, cells and expression vector

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6228646B1 (en) * 1996-03-07 2001-05-08 The Regents Of The University Of California Helper-free, totally defective adenovirus for gene therapy
US20020086411A1 (en) * 1999-06-21 2002-07-04 Holm Per Sonne Agents for treating malignant diseases using the protein YB-1
US6475480B1 (en) * 1998-07-07 2002-11-05 Transgene S.A. Use of adenoviral E4 reading frames to improve expression of a gene of interest
US20030095989A1 (en) * 2000-12-18 2003-05-22 Irving John M. Chimeric cytolytic viruses for cancer treatment
US20060099178A1 (en) * 2002-05-27 2006-05-11 Holm Per S Novel use of adenoviruses and nucleic acids coding therefor
US20060270016A1 (en) * 2003-11-14 2006-11-30 Holm Per S Novel adenoviruses, nucleic acids that code for the same and the use of said viruses
US20070110719A1 (en) * 2003-11-14 2007-05-17 Holm Per S Novel use of adenoviruses and nucleic acids that code for said viruses
US20070116670A1 (en) * 2001-10-16 2007-05-24 Per Sonne Holm Use of the adenoviral e2 promoter
US20070202524A1 (en) * 1999-10-15 2007-08-30 Canji, Inc. Targeted Vectors

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU718772B2 (en) * 1995-03-24 2000-04-20 Genzyme Corporation Adenovirus vectors for gene therapy
AU2145300A (en) * 1998-11-18 2000-06-05 Canji, Inc. Adenoviral vectors
AU6425800A (en) * 1999-06-30 2001-01-22 Max-Delbruck-Centrum Fur Molekulare Medizin Agents for the diagnosis, prognosis and treatment of malignant diseases
US6955808B2 (en) * 1999-09-24 2005-10-18 Uab Research Foundation Capsid-modified recombinant adenovirus and methods of use
US7048920B2 (en) * 2000-03-24 2006-05-23 Cell Genesys, Inc. Recombinant oncolytic adenovirus for human melanoma
EP1446479B1 (en) * 2001-09-29 2012-08-15 Chae-Ok Yun Recombinant adenovirus with enhanced therapeutic effect and pharmaceutical composition comprising said recombinant adenovirus
AU2003271738C1 (en) * 2002-04-25 2008-04-17 Crucell Holland B.V. Stable adenoviral vectors and methods for propagation thereof
KR101123510B1 (ko) * 2002-10-15 2012-04-12 페르 손네 홀름 신규한 아데노바이러스, 이를 암호화하는 핵산 및 이들의 조성물
WO2004035616A2 (de) * 2002-10-15 2004-04-29 Per Sonne Holm Adenovirus mit umgekehrter reihenfolge der expression von genen und verwendung davon
US20050118676A1 (en) * 2003-03-19 2005-06-02 Yan Qi Gene therapy vectors having reduced immunogenicity
JP4871726B2 (ja) * 2003-04-28 2012-02-08 ナノシス・インク． 超疎液性表面、その作製法及び用途
EP1830864A2 (de) 2004-12-31 2007-09-12 Per Sonne Holm E1 -minus adenoviren und deren verwendung
US20070292396A1 (en) * 2006-03-02 2007-12-20 Juan Fueyo Combination therapy with oncolytic adenovirus

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6228646B1 (en) * 1996-03-07 2001-05-08 The Regents Of The University Of California Helper-free, totally defective adenovirus for gene therapy
US6475480B1 (en) * 1998-07-07 2002-11-05 Transgene S.A. Use of adenoviral E4 reading frames to improve expression of a gene of interest
US20020086411A1 (en) * 1999-06-21 2002-07-04 Holm Per Sonne Agents for treating malignant diseases using the protein YB-1
US20070202524A1 (en) * 1999-10-15 2007-08-30 Canji, Inc. Targeted Vectors
US20030095989A1 (en) * 2000-12-18 2003-05-22 Irving John M. Chimeric cytolytic viruses for cancer treatment
US20070116670A1 (en) * 2001-10-16 2007-05-24 Per Sonne Holm Use of the adenoviral e2 promoter
US20060099178A1 (en) * 2002-05-27 2006-05-11 Holm Per S Novel use of adenoviruses and nucleic acids coding therefor
US20060270016A1 (en) * 2003-11-14 2006-11-30 Holm Per S Novel adenoviruses, nucleic acids that code for the same and the use of said viruses
US20070110719A1 (en) * 2003-11-14 2007-05-17 Holm Per S Novel use of adenoviruses and nucleic acids that code for said viruses
US20100297731A1 (en) * 2003-11-14 2010-11-25 Per Sonne Holm Novel adenoviruses, nucleic acids that code for the same and the use of said viruses
US20100311145A1 (en) * 2003-11-14 2010-12-09 Per Sonne Holm Novel use of adenoviruses and nucleic acids that code for said viruses

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11077156B2 (en) 2013-03-14 2021-08-03 Salk Institute For Biological Studies Oncolytic adenovirus compositions
US11130968B2 (en) 2016-02-23 2021-09-28 Salk Institute For Biological Studies High throughput assay for measuring adenovirus replication kinetics
US11401529B2 (en) 2016-02-23 2022-08-02 Salk Institute For Biological Studies Exogenous gene expression in recombinant adenovirus for minimal impact on viral kinetics
US20180099014A1 (en) * 2016-10-07 2018-04-12 Miami University Engineered oncolytic viruses containing hyper-binding sites to sequester and suppress activity of oncogenic transcription factors as a novel treatment for human cancer
US10813957B2 (en) * 2016-10-07 2020-10-27 Miami University Engineered oncolytic viruses containing hyper-binding sites to sequester and suppress activity of oncogenic transcription factors as a novel treatment for human cancer
US11813337B2 (en) 2016-12-12 2023-11-14 Salk Institute For Biological Studies Tumor-targeting synthetic adenoviruses and uses thereof

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US20220339219A1 (en) 2022-10-27

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