CN1603404A - Oncolytic adenovirus with target for liver cancer and its preparation method and use - Google Patents

Abstract

The invention discloses a kind of liver cancer target tropism to dissolve the lump adenovirus, its preparation method and use. The invention adenovirus is starts sub- AF0.3 using oxygen deficit reply part HRE and the AFP core to construct mixed and the start, constructs the retention to have the E1 duplication start area gene the reorganization adenovirus shuttle material particle, again constructs the reorganization adenovirus material particle after the homologous reorganization, the extension dyes the cell, the packing leaves the goal reorganization virus pellet. The invention adenovirus has the liver cancer target tropism, can oneself duplicate in the liver cancer cell, achieves the decomposition cancer cell the goal. Has highly effective, not sends the sudden change function, the safe highly effective merit, may use in to prepare the cancer cell the treatment medicine.

Description

A kind of hepatoma targeting character oncolytic adenovirus, Preparation Method And The Use

Technical field

The present invention relates to a kind of recombinant adenovirus, relate in particular to a kind of hepatoma targeting character oncolytic adenovirus, also relate to this viral Preparation method and use.

Background technology

Onset of liver cancer rate and mortality ratio are high always in China, are the main tumours of harm population of China health, but still do not have the specific treatment method at present.If can develop effective liver cancer biotherapy preparation, not only significant to exploring liver cancer treatment, and have obvious social and economic benefits.

Tumour develop the synergistic result of polygene often, only depend on the gene therapy method of 1 of recovery or several cancer suppressor gene functions generally to be difficult to prove effective, the Miller of U.S. Birmingham University of Alabama and Curiel have delivered one piece of editorial in 1996 on " Gene Therapy " magazine, at first propose the use tumour and selected replicability adenovirus (tumor selective replication Adenovirus, TSRA, also claim specificity oncolytic adenovirus selectively oncolytic Adenovirus) treatment tumour New Policy, in case this recombinant adenovirus infected tumor cell can be at time multiplexed cell system propagation and cracking tumour cell, the virion that discharges after the lysis is other tumour cell of subinfection again, up to whole tumour cells are killed.But should virus in normal cell, can not breed, little to normal primary cellular defect.As the practice of this strategy, Khuri equals to use in 2000 replicability recombinant adenovirus ONYX-015 (d11520) the selective splitting P53-tumour cell of E1b55 disappearance, obtains encouraging success.This research group reports on " natural medical science " magazine in August, 2000: tried out the adenoviral mutants ONYX-015 of the tumour cell that selectivity attacks the P53 defective on one's body and united conventional chemotherapy 30 patients that suffer from the incidence cancer, 25 patients' tumour is dwindled, wherein 8 patients' tumour completely dissolve.The William of the pioneer University of Southern California in gene therapy field. the Anderson is commented on: this achievement is very exciting, because this is to obtain the result that a large amount of tumours disappears and do not recur first in the phase ii clinical trial that the more patient of quantity participates in.ONYX-015 also has been used for the gene therapy research of liver cancer, only the p53-liver cancer cell there is splitting action although generally believe ONYX-015, but also have result of study to find that ONYX-015 can duplicate in p53+ hepatoma cell line such as HepG2, p53 state and ONYX-015 duplicate the shortage dependency.The multiple virus of proliferation of adenoviral mutants ONYX-015 etc. recent years has entered clinical trial, for tumor treatment has been opened up a new research field.

Selecting the replicability adenovirus why good curative effect is arranged, mainly is because adenovirus energy self-replicating is logarithmic proliferation, makes its therapeutic dose become ten thousand times of ground to amplify.In the adenovirus oncolytic therapy, select the replicability adenovirus to seek target cell on one's own initiative, in target cell, duplicate, the cancer cells cracking is killed.

AdE1 district gene is the promotor gene that duplicates of adenovirus, comprises E1a and E1b two portions, and can whether its expression is directly connected to adenovirus be duplicated.If therefore whole adenovirus is likened to a machine, the E1 district is exactly the master switch of this machine so, and its effect is most important.In initial 2.5 hours after adenovirus infection, have only the E1a gene to be transcribed, translate, this albumen can activate the essential various cytogenes of adenoviral replication and the expression of virogene.Used in the past replication-defective adenoviral has been rejected this section sequence just.And in selecting the replicability adenovirus, keep just and utilize this gene regions, be placed under the regulating and controlling sequence control of tumor tissues or cell-specific, or utilize distinctive signal transduction path in the tumour cell, make virus replication and reach the purpose that cancer cells is killed in special cracking.

A right matter of utmost importance of the gene therapy demand side of tumour is target or specificity.People are for killing tumor cell specifically, and according to the biological characteristics of tumour cell, the singularity of genetic expression in the distribution of the acceptor molecule of cell surface and the born of the same parents has designed the method for some targets.As be used for the retroviral vector of central nerve neuroma more, and promptly be to have utilized its special character that is integrated in somatoblast, goal gene is imported just at the splitted tumour cell.Adenoviral mutants ONYX-015 has utilized the p53 gene product of sudden change in the tumour cell can not stop the cell to enter replicative phase and can allow it to breed simultaneously to duplicate, cause the cancer cells cracking at last.At present, investigators generally adopt a method that has flexibly broad sense, promptly select for use tumour-specific controlling element (promotor and enhanser) with driving purposes genetic expression in specific target cell.This method has been used for the experimental study of solid tumors such as liver cancer, lung cancer, cancer of the stomach, ovarian cancer, carcinoma of the pancreas, mammary cancer, prostate cancer, colorectal cancer, osteosarcoma, melanoma.In the face of target or specificity problem, the structure of specificity oncolytic adenovirus also adopts tumour-specific controlling element (promotor and enhanser) to drive adenovirus and duplicates in specific target cell the adenovirus oncolytic therapy mostly too.

In theory, can make up TSRAd by each link that regulating and controlling adenovirus duplicates; Studies show that in fact in recent years, main strategy is with regard to three kinds: the one, and unnecessary gene when rejecting (all or part of) adenovirus and in tumour cell, duplicating, and these genes are essential in normal cell, as by combining and the gene in activating cells cycle with p53 or Rb; Second kind of strategy then is to replace natural viral promotors with control virus replication expression of gene with TS promotor; The 3rd, transform the adenovirus cilia protein, make its infected tumor and duplicating therein specifically.

In the liver cancer suicide gene therapy studies of retroviral vector mediation, with the anoxic response element HRE of vascular endothelial growth factor VEGF upstream and the hybrid promoter HREAF of AFP core promoter AF0.3 formation, can instruct suicide gene HSV tk in nearly all generation or do not produce specificity overexpression in (as HLF) hepatoma cell line of AFP, enhanser HRE has optionally activated the trace AFP promoter activity in the liver cancer cell that does not produce AFP under anoxia condition.Therefore, hybrid promoter HREAF has expanded the range of application of AFP promotor in hepatoma targeting character or specific gene treatment greatly.But in the liver cancer suicide gene therapy of this retroviral vector mediation, owing to there be " bystander effect ", liver stem cells still can be involved unavoidably, and the liver reserve capabillity can be affected.

By retrieval, at present rarely seen retroviral vector that has structure to contain AFP alpha-fetoprotein and HRE anoxic response element abroad, and the adenovirus carrier that does not have the E1 district disappearance of hepatoma targeting character, do not see as yet and make up the report that hepatoma targeting character reproducibility oncolytic adenovirus carries out gene therapy of liver cancer.

Summary of the invention

The oncolytic adenovirus that the purpose of this invention is to provide a kind of hepatoma targeting character, and the Preparation method and use of this adenovirus.

Hepatoma targeting character oncolytic adenovirus of the present invention comprises the hybrid promoter HREAF of the hepatoma targeting character that anoxic response element HRE and AFP core promoter AF0.3 make up, and the adenovirus E 1 district duplicates promotor gene, and the downstream that promotor gene is positioned at the hepatoma targeting character hybrid promoter is duplicated in the adenovirus E 1 district.

The present invention adopts shuttle plasmid to make up the recombinant adenovirus shuttle plasmid, and again through the homologous recombination construction recombinant adenovirus plasmid, purified, enzyme is cut, and transfectional cell is packed out purpose recombinant adenovirus particle.

The preparation method of hepatoma targeting character oncolytic adenovirus of the present invention may further comprise the steps:

1, clone HRE and AF0.3 and structure hybrid promoter HREAF

(1) the PCR primer of design anoxic response element HRE, AFP core promoter AF0.3 is a template with the human hepatocellular carcinoma cell genomic dna, carries out pcr amplification.

(2) with the PCR product cloning to pGEM-T easy carrier, make up plasmid pGEM-HRE and pGEM-AF0.3.

(3) carry out PCR and enzyme and cut the evaluation of identifying and check order.

(4) structure of hybrid promoter HREAF.HRE and AF0.3 are carried out pcr amplification, after recovery PCR product and purifying, enzyme are cut,, get hybrid promoter HREAF in external connection.

2, make up adenovirus shuttle plasmid pShuttle-HREAF-E1 and pShuttle-HREAF-E1 Δ 55

The required bacterium homologous recombination system of recombinant adenovirus comprises E.coli BJ5183 (Stratagene company product) and shuttle plasmid pShuttle, pShuttle-CMV and adenovirus skeleton plasmid pAdEasy-1.PShuttle can comprise the complete genome of regulating and controlling sequence to the polyA tailing signal for inserting, and pShuttle-CMV then can only contain the encoding sequence of translation initiation password to termination codon for inserting.But in the present invention, need in shuttle vectors, insert regulating and controlling sequence HREAF, encoding sequence AdE1 or the AdE1 Δ 55 of different sources, and need provide polyA tailing signal for it.Therefore shuttle plasmid pShuttle-HREAF-E1 that will make up among the present invention and pShuttle-HREAF-E1 Δ 55 all can not directly make up on the basis of pShuttle or pShuttle-CMV, need earlier it to be changed structure, the present invention is chosen in and inserts the polyA tailing signal among the pShuttle.Change the structure route as shown in Figure 3.

(1) the design shuttle plasmid makes up required primer.

(2) structure of recombinant adenovirus shuttle plasmid pShuttle-HREAF-E1 and evaluation.Adenovirus shuttle vector pShuttle and pShuttle-CMV are carried out enzyme respectively cut, connect endonuclease bamhi and transform, obtain in pShuttle, to have inserted the recombinant adenovirus shuttle plasmid pShuttle-R of SV40 tailing signal sequence;

The PCR product of pShuttle-R and HREAF is carried out enzyme respectively cut, connect endonuclease bamhi and transform, obtain in pShuttle-R, to have inserted the recombinant adenovirus shuttle plasmid pShuttle-HREAF of regulating and controlling sequence HREAF;

The PCR product of pShuttle-HREAF and AdE1 is carried out double digestion respectively, connect endonuclease bamhi and conversion, the recombinant adenovirus shuttle plasmid pShuttle-HREAF-E1 of adenovirus AdE1 gene has been inserted in acquisition in pShuttle-HREAF, adopt PCR and enzyme blanking method to identify.

(3) structure of pShuttle-HREAF-E1 Δ 55 and evaluation

Because the capacity packing of adenovirus is limited, can wrap the liver cancer-specific oncolytic adenovirus that can hold in order to construct adenovirus capsid, the present invention has made up pShuttle-HREAF-E1 Δ 55.The structure route of pShuttle-HREAF-E1 Δ 55 is similar to pShuttle-HREAF-E1.

The PCR product of AdE1 Δ 55 genes of pShuttle-HREAF and disappearance E1b55 is carried out enzyme respectively cut, connect endonuclease bamhi and transform, obtain recombinant adenovirus shuttle plasmid pShuttle-HREAF-E1 Δ 55, adopt PCR and enzyme blanking method to identify.

3, produce recombination oncolytic adenovirus AdhafE1 Δ 55

(1) adopt AdEasy XL adenoviral vector system (Stratagene company product) to produce the principle of recombinant adenovirus, the long 33.5kb of skeleton plasmid pAdEasy-1 in this system, reject E1 district and E3 district, contained ampicillin resistance gene; Be cloned into shuttle plasmid such as pShuttl-HREAF-E1 and the long respectively 10.45kb of pShuttl-HREAF-E1 Δ 55 and the 9.3kb of external source goal gene, all contained kalamycin resistance gene.Skeleton plasmid and shuttle plasmid all contain the pBR322 replication origin, can duplicate amplification in bacterium.

The shuttle plasmid that builds is carried out linearizing, carry out homologous recombination, select, cut evaluation through vitro enzyme again through antibiotics resistance with pAdEasy-1 transformed competence colibacillus bacterium.Recombinant adenovirus plasmid after the evaluation is transformed to the recombination deficient mutant bacterial strain and increases in a large number.Recombinant adenovirus plasmid behind the purifying is cut through enzyme, exposes left and right sides inverted repeats (ITR) back transfectional cell, packs out purpose recombinant adenovirus particle.

(2) generation of recombinant adenovirus plasmid and evaluation in the bacterium

With shuttle plasmid pShuttl-HREAF-E1 and 55 linearizings of pShuttl-HREAF-E1 Δ, respectively with skeleton plasmid pAdEasy-1 transformed competence colibacillus bacterium, the dull and stereotyped selection of microbiotic cultivated, and the recombinant plasmid pAdhafE1 or the pAdhafE1 Δ 55 that only possess kalamycin resistance can be selected.Choose pAdhafE1 clone and pAdhafE1 Δ 55 clones respectively, the extracting plasmid carries out enzyme and cuts evaluation.

(3) produce adenovirus in the mammalian cell

The contriver selects recombinant plasmid pAdhafE1 Δ 55 to carry out the packing production of recombinant adenovirus AdhafE1 Δ 55.With recombinant plasmid pAdhafE1 Δ 55 increase in a large number, purifying, cut through enzyme, expose transfection mammalian cell (as 293 cells) behind the ITR of the left and right sides, carry out the packing of recombinant adenovirus particle AdhafE1 Δ 55.Treat that complete pathology appears in cell, reclaim cell, extract the recombinant adenovirus genomic dna,, carry out PCR and identify, set up negative control simultaneously as template.

4, the specific killing effect of 55 pairs of human liver cancer cells of AdhafE1 Δ

(1) specific killing of 55 pairs of human liver cancer cells of morphological observation AdhafE1 Δ

With human liver cancer cell and lung carcinoma cell bed board, to attack respectively with low dosage oncolytic adenovirus AdhafE1 Δ 55, anoxia condition is cultivated down, the observation of cell growing state.

(2) the MTT experiment detects the specific killing of 55 pairs of human liver cancer cells of AdhafE1 Δ

With human liver cancer cell and lung carcinoma cell bed board, attack respectively with low dosage oncolytic adenovirus AdhafE1 Δ 55, cultivate under the hypoxia inducible condition.Measure the absorbance value of each porocyte respectively, draw cell growth curve, and each tumour cell carried out the survival state of AdhafE1 Δ 55 between whether infecting relatively on each time point, and on each time point, carrying out the comparison of survival rate between each tumour cell.

(3) RT-PCR detects the expression of E1a

With AdhafE1 Δ 55 difference infected person liver cancer cell and lung carcinoma cells, cultivate collecting cell, extract total RNA, detect the expression of E1a with RT-PCR.

It is its supply oxygen and nutritive substance that the progress of tumour need be set up new vessel, possesses the precondition that the vascularization ability also just becomes tumor growth.In promoting numerous factors that tumor neogenetic blood vessels generates, VEGF has played the part of extremely important role, and its expression is to come inductive by the HRE that is present in its gene 5 ' end upstream under anoxia condition.HRE induces goal gene to strengthen under anoxia condition and expresses, and has tissue or cell-specific, and its tissue or cell-specific are limited by the promotor with its next-door neighbour.Liver cancer is considered to the tumour of high vascularity, but finds that still it expresses higher levels of VEGF than corresponding nonneoplastic tissue.The liver cancer-specific that the promotor HREAF that observations such as Ido are formed by HRE and AF0.3 heterozygosis mediates, the enhancing that also proves enhanser HRE inductive goal gene under anoxia condition is expressed and can be activated sub-AF0.3 and be defined in (Ido A in the liver cancer cell, Uto H, Moriuchi A, et al.Genetherapy targeting tor hepatocellular carcinoma:selective and enhanced suicidegene expression regulated by a hypoxia-inducible enhancer linked to a human α-fetoprotein promoter.Cancer Research, 2001; 61:3016-3021).

According to the characteristics of liver cance high-expression VEGF and efficient, the rigorous liver cancer-specific of hybrid promoter destination gene expression that HREAF mediates, if with HREAF be used to instruct oncolytic adenovirus in liver cancer cell special duplicate and cracking it, then can have " duplicating and the cracked one-to-one relationship " characteristics because of the specificity oncolytic adenovirus, and can avoid influence at least in theory to the liver reserve capabillity, reach the requirement of specific killing liver cancer cell as much as possible.Because the liver regeneration process then is orderly appropriate feature, oxygen is for sufficient, be different from tissues such as hepatitis, liver cirrhosis the expression that can mediate VEGF, also be different from solid tumor and can increase too fast and unordered new green blood for causing because of the knurl body mainly by anoxia condition mediation vegf expression by anoxia condition and the various kinds of cell factor and somatomedin.

The present invention adopts and selects replicability adenovirus oncolytic strategy to carry out gene therapy of liver cancer, in order to solve target or the specificity problem in the gene therapy of liver cancer, and the liver cancer that does not as far as possible wait at all AFP output, the contriver has made up the hepatoma targeting character oncolytic adenovirus AdhafE1 Δ 55 that hybrid promoter HREAF instructs, and carried out preliminary external liver-cancer cell specific and killed and wounded research, obtained the specific killing result to liver cancer cell of expection.Utilize recombinant adenovirus of the present invention, can prepare the medicine that is used for the treatment of liver cancer.Recombinant adenovirus of the present invention can be used as one of selection of liver cancer biotherapy, for liver cancer patient brings glad tidings.

Innovative point of the present invention is to replace retroviral with the reproducibility oncolytic adenovirus, reach the purpose of cracking target cell by duplicating of adenovirus itself, compare with replication-defective adenoviral, the present invention keeps and has utilized adenoviral replication promotor gene AdE1 gene, makes virus replication and reaches the purpose that cancer cells is killed in special cracking.And have the following advantages: 1, target cell not necessarily can be killed and wounded the efficient height duplicating division stage.2, adenovirus is not inserted target cell nuclear gene group, no mutagenesis.3, one property crossed effects, safe.

Description of drawings

Fig. 1 is the pGEM-HREAF structural representation.

Fig. 2 makes up synoptic diagram for hybrid promoter HREAF.

Fig. 3 makes up synoptic diagram for recombinant plasmid pShuttle-HREAF-E1.

Fig. 4 is that recombinant plasmid pShuttle-HREAF-E1 Δ 55 makes up synoptic diagram.

Fig. 5 is that AdEasy XL adenoviral vector system produces the recombinant adenovirus synoptic diagram.

Fig. 6 cuts evaluation for the enzyme of recombinant adenovirus plasmid pAdhafE1, wherein

1,3 for before enzyme cuts, and 2,4 for after the PacI enzyme cuts, and 5 is that DNA marker λ-Hind III Fig. 7 is plasmid pAdhafE1 Δ 55 electrophorograms, wherein

1,2,3,5,6,7 is that plasmid pAdhafE1 Δ 55,4 is identified pAdhafE1 Δ 55 figure for DNA marker λ-Hind III Fig. 8 cuts for the PacI enzyme, wherein

1,2,3,5,6,7 cut product for the PacI enzyme of pAdhafE1 Δ 55, and 4 is DNA marker λ-Hind III

Fig. 9 is cytopathic effect figure, and a is the pathology porocyte among the figure, and b is the control wells cell.

Figure 10 is the genomic dna of recombinant adenovirus AdhafE1 Δ 55, wherein

1 is DNA Marker λ-HindIII digest,

2 is the AdhafE1 Δ of packing out in 293 cells 55,

3 is the AdhafE1 Δ of packing out in the HepG2 cell 55.

Figure 11 is that the PCR of recombinant adenovirus AdhafE1 Δ 55 identifies electrophorogram, wherein

1 is DNA Marker DL2000

2 for being template pcr amplification HREAF with the recombinant adenovirus genomic dna of packing out in 293 cells

3 for being template pcr amplification HREAF with the recombinant adenovirus genomic dna of packing out in the HepG2 cell

4 negative contrasts

Figure 12 is the specific killing action diagram of 55 pairs of human liver cancer cells of AdhafE1 Δ, wherein

A is Be17402 cell/AdhafE1 Δ 55,

B is contrast Be17402 cell,

C is HepG2 cell/AdhafE1 Δ 55,

D is contrast HepG2 cell,

E is a PLA801C/AdhafE1 Δ 55,

F is contrast PLA801C.

Figure 13 infects survival curve figure behind the AdhafE1 Δ 55 for liver cancer cell.

Figure 14 detects the specifically expressing figure that AdhafE1 Δ 55 infects E1a behind the liver cancer cells for the RT-PCR method,

Wherein

1,2,3 are respectively the G3PDH RT-PCR product of HepG2, Bel7402 and PLA801C cell

4 is DNA Marker DL2000,

5,6,7 are respectively the E1a RT-PCR of HepG2, Bel7402 and PLA801C cell.

Embodiment

Embodiment one clone HRE and AF0.3 and structure hybrid promoter HREAF

1, from Genbank, finds the sequence of human vascular endothelial growth factor VEGF upstream anoxic response element HRE and people's α-Jia Taidanbai core promoter AF0.3, and carry out the analysis of inner restriction enzyme site

(1) contain anoxic response element HRE sequence for seeing GenBank data accession no.M63971, in the sequence between SacI and the PstI (1188-1572) about 380bpDNA fragment be anoxic response element HRE.

(2) contain α-Jia Taidanbai core promoter AF0.3 sequence for seeing GenBank data accessionno.L34019, the 259bpDNA fragment in the sequence between 723～981 is AFP core promoter AF0.3.Design the PCR primer of anoxic response element HR, AFP core promoter AF0.3, anoxic response element HRE primer: upstream primer is seen sequence 1 in the sequence table, and downstream primer is seen sequence 2 in the sequence table.Insert the HindIII site at its upstream in the primer, be convenient to insert subsequently enhancer sequence, insert the BamHI site in the downstream primer, be beneficial to follow-up connection, clone operations.The about 560bp of expection amplified production.

AFP core promoter AF0.3 primer: upstream primer is seen sequence 3 in the sequence table, and downstream primer is seen sequence 4 in the sequence table.Insert the BamHI site at its upstream in the primer, be convenient to insert subsequently enhancer sequence, insert the HindIII site in the downstream primer, be beneficial to follow-up connection, clone operations.The about 310bp of expection amplified production.

3, the pcr amplification of anoxic response element HRE, AFP core promoter AF0.3

With human hepatocellular carcinoma HepG2 cell (available from Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences) genomic dna is template, carry out the high-fidelity pcr amplification of HRE and AF0.3 respectively with the primer of design, electrophoresis observation, as seen have an appointment the respectively amplified band of 310bp and 560bp, and be primary product, consistent with expected result.

4, with the PCR product cloning of anoxic response element HRE, AFP core promoter AF0.3 to pGEM-T easy carrier, make up plasmid pGEM-HRE and pGEM-AF0.3.

With the above-mentioned PCR product of HRE and AF0.3 behind ethanol sedimentation, add the A tail with the Taq archaeal dna polymerase, link to each other with the T carrier then, transform JM109 host bacterium (Stratagene company product), be laid in the agar plate that contains X-gal, IPTG, Amp, the result grows many bluenesss and white colony.White colony is the candidate clone.

5, PCR and the enzyme of anoxic response element HRE, AFP core promoter AF0.3 are cut evaluation

Respectively choose white clone, pyrolysis method prepares plasmid and makes template, carries out the pcr amplification of HRE and AF0.3 respectively with special primer, electrophoresis observation, and the clone of visible picking all can amplify the purpose fragment of about 310bp and 560bp.Extract plasmid pGEM-HRE and pGEM-AF0.3, carry out the BamHI+HindIII double digestion and identify, but visible plasmid pGEM-HRE enzyme cuts out the purpose fragment of about 560bp, but the pGEM-AF0.3 enzyme cuts out the purpose fragment of about 310bp.

Cut qualification result in conjunction with above PCR and enzyme to plasmid pGEM-HRE and pGEM-AF0.3, the restriction enzyme site and the size that show the anoxic response element HRE, the AFP core promoter AF0.3 that are cloned into pGEM-T easy carrier are correct, send pGEM-AF0.3 and pGEM-HRE plasmid to give birth to the order-checking of worker company to Shanghai.

6, order-checking is identified

Anoxic response element HRE, AFP core promoter AF0.3 have checked order partly consistent with bibliographical information, add HindIII and BamHI restriction enzyme site at two ends respectively, can determine the direction of insertion of exogenous dna fragment HRE and AF0.3 among plasmid pGEM-HRE and the pGEM-AF0.3.

7, the structure of hybrid promoter HREAF

HRE and AF0.3 are carried out pcr amplification, after reclaiming PCR product and purifying, enzyme and cutting, connect external, hybrid promoter HREAF, this is connected product cloning to pGEM-T easy carrier, as Fig. 1 institute not, through PCR, enzyme cut and check order identify correct.

For the ease of the structure of HREAF, other has designed an AF0.3 downstream primer, has brought the SphI site into, shown in sequence in the sequence table 14.The structure route of hybrid promoter HREAF as shown in Figure 2, the connection product HREAF that expection can about 700bp.

Connect product as template with HREAF, with HRE upstream primer and the pairing of AF0.3 downstream primer, carry out pcr amplification, the result is consistent with expection.

According to the analysis of HRE and AF0.3 sequence restriction enzyme site and the structure route of HREAF, can be expected to connect among the product HREAF to have two SacI sites, at a distance of about 445bp.Therefore after the HREAFPCR product purification being reclaimed, carry out single endonuclease digestion with SacI, the result is as expection institute material, and enzyme has cut out 445bp specific fragment in the middle part of the HREAF sequence and the band of about respectively 200bp in two ends and 50bp.

HREAF PCR product behind ethanol sedimentation, is added the A tail with the Taq archaeal dna polymerase, link to each other with the T carrier then, transform JM109 host bacterium, be laid in the agar plate that contains X-gal, IPTG, Amp, the result grows many bluenesss and white colony.White colony is the candidate clone.Choose white clone, pyrolysis method prepares plasmid and makes template, carries out the pcr amplification of HREAF respectively with special primer, and as seen electrophoresis observation amplifies the purpose fragment of about 700bp.

Little upgrading grain pGEM-HREAF carries out EcoR I single endonuclease digestion and identifies that enzyme cuts out the purpose fragment of about 700bp as a result.

Cut qualification result in conjunction with above PCR and enzyme to HREAF connection product and plasmid pGEM-HREAF, the restriction enzyme site and the size that show the hybrid promoter HREAF that is cloned into pGEM-T easy carrier are correct, send the pGEM-HREAF plasmid to adopt the T7 universal primer mensuration that checks order to brilliant safe biotech company, the HREAF sequencing result is shown in sequence in the sequence table 5, anoxic response element HRE wherein, AFP core promoter AF0.3 is consistent with bibliographical information respectively, meet expection and make up imagination, can determine that the direction of insertion of exogenous dna fragment HREAF among the plasmid pGEM-HREAF is distinguished as shown in the figure.

Embodiment two adenovirus shuttle plasmid pShuttle-HREAF-E1 and

The structure of pShuttle-HREAF-E1 Δ 55

1, the design shuttle plasmid makes up required primer

According to the anoxic response element HRE that reports in the document (GenBank data accession no.M63971), AFP core promoter AF0.3 (GenBank data accession no.L34019), the sequence (www.stratagene.com of Stratagene company's site) at adenovirus E 1 a and E1b (GenBank data accession no.X02996) and shuttle plasmid pShuttle multiple clone site (MCS) two ends, design primer respectively, and look the needs of vector construction, add different restriction endonuclease sites respectively at its 5 ' end or 3 ' end, be used for respectively making up the pcr amplification of element, primer is synthetic by match hundred victory companies.

The HREAF primer: upstream primer adds the KpnI site shown in sequence in the sequence table 6, and downstream primer adds the XhoI site shown in sequence in the sequence table 7, and expection amplification purpose product is about 720bp;

The E1a primer: upstream primer is shown in sequence in the sequence table 8, add the XhoI site, downstream primer is shown in sequence in the sequence table 9, and expection amplification purpose product is 1000bp (in RT-PCR, may amplify the cDNA band of about 1000bp, 880bp or 740bp);

The E1b primer: downstream primer adds the EcoRV site shown in sequence in the sequence table 10.With the pairing of E1a upstream primer, expection amplification purpose product is 2950bp, is total length AdE1;

E1b Δ 55 primers: downstream primer adds EcoR V site shown in sequence in the sequence table 11.With the pairing of E1a upstream primer, expection amplification purpose product is 1720bp, is AdE1 Δ 55 genes of disappearance E1b55;

PShuttle MCS two ends primer: upstream primer is shown in sequence in the sequence table 12, and downstream primer is shown in sequence in the sequence table 13, and expection amplification purpose product size is decided according to inserting segmental size; Each time PCR reaction conditions is decided according to primer collocation service condition and purpose product size.

2, the structure of recombinant adenovirus shuttle plasmid pShuttle-HREAF-E1

Adenovirus shuttle vector pShuttle and pShuttle-CMV are carried out Xho I and EcoR I double digestion respectively, reclaim the big fragment in purifying pShuttle source and the small segment in pShuttle-CMV source respectively, the T4 ligase enzyme connects and transformed competence colibacillus cell JM109, screening positive clone, cut evaluation through PCR and enzyme, obtain in pShuttle, to have inserted the recombinant adenovirus shuttle plasmid pShuttle-R of SV40 tailing signal sequence.The PCR product of pShuttle-R and HREAF is carried out Xho I and Kpn I double digestion respectively, connect, transform, screen, identify as above-mentioned method behind the ethanol sedimentation, obtain in pShuttle-R, to have inserted the recombinant adenovirus shuttle plasmid pShuttle-HREAF of regulating and controlling sequence HREAF.The PCR product of pShuttle-HREAF and AdE1 is carried out Xho I and EcoR V double digestion respectively, connect, transform, screen, identify as above-mentioned method behind the ethanol sedimentation, obtain in pShuttle-HREAF, to have inserted the recombinant adenovirus shuttle plasmid pShuttle-HREAF-E1 of adenovirus AdE1 gene.Each plasmid of above-mentioned structure is carried out PCR and enzyme respectively cut evaluation.

3, the structure of pShuttle-HREAF-E1 and evaluation

With above-mentioned each plasmid as template, carry out the PCR evaluation with pShuttle MCS two ends primer to inserting fragment, as seen it is long that pShuttle changes the 150bp that only has an appointment between the preceding MSC two ends of structure, change the pShuttle-R behind the structure owing to inserted the long SV40 tailing signal sequence of about 230bp, distance becomes about 380bp and grows between the MSC two ends; After inserting HREAF, spacing further becomes about 1080bp; After having inserted E1, spacing finally becomes about 4000bp.With pShuttle-HREAF-E1 is template, respectively with special primer to amplification HREAF, E1 and HREAF-E1, can expect that size is about the special external source fragment of 700bp, 2950bp and 3650bp respectively.

When with above-mentioned each plasmid of Kpn I and EcoR V double digestion, can obtain two bands identical with pShuttle endonuclease bamhi size with external source purpose fragment HREAF at pShuttle-HREAF; But because there is the KpnI restriction endonuclease sites E1 inside, thus obtained three bands at pShuttle-HREAF-E1, only wherein one identical with pShuttle endonuclease bamhi size; If but used XhoI and EcoR V double digestion instead, then could obtain two bands identical with EcoRV double digestion clip size with the XhoI of external source purpose fragment E1 and pShuttle-HREAF at pShuttle-HREAF-E1.

Above PCR and enzyme are cut qualification result and are shown that pShuttle-R, pShuttle-HREAF and pShuttle-HREAF-E1 make up correctly.

4, the structure of pShuttle-HREAF-E1 Δ 55 and evaluation

The structure route of pShuttle-HREAF-E1 Δ 55 is similar to pShuttle-HREAF-E1, just the E1 PCR product that pShuttle-HREAF-E1 is made up in the synoptic diagram (see figure 3) changes E1 Δ 55PCR product into, and the shuttle plasmid structural representation that is built into is at last seen Fig. 4.

The PCR product of pShuttle-HREAF and AdE1 Δ 55 genes of disappearance E1b55 is carried out XhoI and EcoR V double digestion respectively, connect, transform, screen, identify as above-mentioned method behind the ethanol sedimentation, obtain in pShuttle-HREAF, to have inserted the recombinant adenovirus shuttle plasmid pShuttle-HREAF-E1 Δ 55 of adenovirus AdE1 Δ 55 genes.

After pShuttle-HREAF-E1 Δ 55 process PCR and enzyme are cut evaluation, this plasmid as template, is carried out PCR with pShuttle MCS two ends primer to whole insertion fragments and identifies that as seen after having inserted E1 Δ 55, spacing finally becomes about 2800bp.To pcr amplification E1 Δ 55, can expect that size is about the special external source fragment of 1720bp with special primer E1a-up+E1b Δ 55-down primer.With XhoI and EcoR V double digestion pShuttle-HREAF-E1 Δ 55, can cut out and the identical specific band of external source purpose fragment E1 Δ 55 clip size by enzyme.PCR and enzyme are cut qualification result explanation pShuttle-HREAF-E1 Δ 55 and are made up correct.

Embodiment three preparation recombination oncolytic adenovirus AdhafE1 Δs 55

1, adopt AdEasy XL adenoviral vector system to produce recombinant adenovirus (Fig. 5)

After shuttle plasmid builds, with its linearizing, transform BJ5183 (Stratagene company product) competence bacterium with skeleton plasmid pAdEasy-1 with PmeI.Two plasmids homologous recombination in thalline, recombinant adenovirus plasmid is selected through kalamycin resistance, cuts evaluation through external PacI enzyme again.Recombinant adenovirus plasmid should produce the big fragment of a treaty 30kb and the small segment of a 3.0kb (reorganization occurs in left arm) or 4.5kb (reorganization occurs in the pBR322 replication origin) after the PacI enzyme is cut.The recombinant adenovirus plasmid of cutting without the PacI enzyme, show as on the 0.8% agarose gel electrophoresis band top near on the faint band at place, sample hole, often also have a just little band below 23kb DNA marker.

Recombinant adenovirus plasmid after the evaluation is transformed to amplification in a large number in recombination deficient mutant bacterial strain such as the JM109.Recombinant adenovirus plasmid behind the purifying can be cut through the PacI enzyme, exposes left and right sides ITR after by Lipofectamine 2000 (Invitragen company) mediation rotaring redyeing 293 cell (Stratagene company product), pack out purpose recombinant adenovirus particle.

2, the generation of recombinant adenovirus plasmid and evaluation in the bacterium

Shuttle plasmid pShuttl-HREAF-E1 and pShuttl-HREAF-E1 Δ 55 respectively with PmeI with its linearizing, transform BJ5183 competence bacterium with skeleton plasmid pAdEasy-1 respectively, be laid on the kalamycin resistance LB flat board and select to cultivate.Homologous recombination between both homologous sequences in this receptor bacterium, therefore plasmid pAdhafE1 and pAdhafE1 Δ 55 after the reorganization possess kalamycin resistance, have only the shuttle plasmid pShuttl-HREAF-E1 that all possesses kalamycin resistance or pShuttl-HREAF-E1 Δ 55 and recombinant plasmid pAdhafE1 or the pAdhafE1 Δ 55 can be selected.Choose pAdhafE1 and pAdhafE1 Δ 55 clones, extracting plasmid, and after cutting with the PacI enzyme, 0.8% agarose gel electrophoresis sees that according to electrophoretic band size evaluation pAdhafE1 recon Fig. 6 and pAdhafE1 Δ 55 recons see Fig. 7, Fig. 8.Can see recombinant adenovirus plasmid pAdhafE1 and the pAdhafE1 Δ 55 cut without the PacI enzyme, show as on the 0.8% agarose gel electrophoresis band top near on the faint band at sample hole place and one the little band below 23kb DNA marker just.After the PacI enzyme was cut, 2 pAdhafE1 recons and 4 pAdhafE1 Δ 55 recons had all produced the big fragment of a treaty 30kb and the small segment of a 4.5kb (reorganization occurs in the pBR322 replication origin); Other has 2 pAdhafE1 Δ 55 recons to produce the small segment of 3.0kb (reorganization occurs in left arm), shows successfully recombinated out in the BJ5183 bacterium liver cancer-specific oncolytic adenovirus plasmid pAdhafE1 and pAdhafE1 Δ 55.

3, produce adenovirus in the mammalian cell

The contriver selects recombinant plasmid pAdhafE1 Δ 55 to carry out the packing production of recombinant adenovirus AdhafE1 Δ 55.

With recombinant plasmid pAdhafE1 Δ 55 increase in a large number, purifying, cut through the PacI enzyme, expose left and right sides ITR after, carry out the packing of recombinant adenovirus particle AdhafE1 Δ 55 by Lipofectamine2000 mediation rotaring redyeing 293 cell; Or transfection HepG 2 cell, (1%O under the hypoxia inducible culture condition ₂, 5%CO ₂And 94%N ₂, 37 ℃) and carry out the packing of recombinant adenovirus particle AdhafE1 Δ 55.

After the transfection the 7th～8 day, pathology appearred in visible cell, as shown in Figure 9.

Lesion region enlarges gradually subsequently, until complete pathology.Cell is reclaimed, freeze thawing three times, releasing virus is inoculated in respectively in 293 cells or the HepG2 cell again, and complete pathology appears in cell after 2 days.Cell is reclaimed, freeze thawing three times, releasing virus, the centrifuging and taking supernatant, extract the recombinant adenovirus genomic dna and see Figure 10,, with the upstream and downstream primer of hybrid promoter HREAF (HRE-up+AF0.3-down) carried out PCR and identify as the template of PCR reaction, setting up simultaneously with the mammalian cell genomic dna is the negative control of template, and the result as shown in figure 11.

Though two integral parts in the hybrid promoter HREAF fragment all exist in the mammalian cell genomic dna, but there is no this heterozygosis fragment of HREAF in the normal mammalian cell genomic dna, therefore can confirm that the recombinant adenovirus of packing out is AdhafE1 Δ 55 in 293 cells or HepG2 cell.

CPE method mensuration recombinant adenovirus AdhafE1 Δ 55 titres are about 2～3 * 10 fast ⁶Pfu/ml.

The specific killing effect of 55 pairs of human liver cancer cells of embodiment four AdhafE1 Δs

The oncolytic adenovirus AdhafE1 Δ of packing out through liver cancer cell HepG2 among the embodiment above using 55 carries out the liver-cancer cell specific fragmentation test of cell in vitro level.

1, the specific killing of 55 pairs of human liver cancer cells of morphological observation AdhafE1 Δ

With 5 * 10 ⁴/ hole human hepatoma cell line HepG2, Bel7402 (available from Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, national ATCC cell bank) and lung cancer cell line PLA801C (national ATCC cell bank is preserved) are laid on 6 orifice plates, with 1 * 10 ⁴Pfu low dosage oncolytic adenovirus AdhafE1 Δ 55 is attacked respectively, (1%O under the hypoxia inducible condition ₂, 5%CO ₂And 94%N ₂, 37 ℃) cultivate.As a result, HepG2, big death of Bel7402 cell after 6 days, the PLA801C cell is then uninfluenced, and growth is normal.The result as shown in figure 12.

2, the MTT experiment detects the specific killing of 55 pairs of human liver cancer cells of AdhafE1 Δ

With 1～2 * 10 ³/ hole human hepatoma cell line HepG2, Bel7402 and lung cancer cell line PLA801C are laid on 96 orifice plates, with 1 * 10 ⁴Pfu low dosage oncolytic adenovirus AdhafE1 Δ 55 is attacked respectively, (1%O under the hypoxia inducible condition ₂, 5%CO ₂And 94%N ₂, 37 ℃) cultivate.Measure the absorbance value of each porocyte respectively at 24h, 48h, 72h and 84h, draw cell growth curve and see Figure 13, and each tumour cell carried out the survival state of AdhafE1/55 between whether infecting relatively on each time point, and on each time point, carrying out the comparison (table 1) of survival rate between each tumour cell.Can find in conjunction with Figure 13 and table 1, human hepatoma cell line HepG2, Bel7402 are after infecting AdhafE1 Δ 55 72h, no matter be with respect to the liver cancer cell of the same race that does not infect AdhafE1 Δ 55, still with respect to the lung carcinoma cell PLA801C that also infects AdhafE1 Δ 55, its survivaling cell number average significantly descends (P＜0.05), does not have difference (P＞0.05) on the statistics and infect and do not infect the survivaling cell number average on each time point between the lung carcinoma cell PLA801C of AdhafE1 Δ 55.MTT result of experiment explanation recombination oncolytic adenovirus AdhafE1 Δ 55 can special cracking, killing hepatoma cell HepG2 and Bel7402.

Table 1 infects the t check of AdhafE1 Δ 55 back tumour cell survival state differences

The different time points survival rate

Tumour cell

24h 48h 72h 84h

HepG2-t/c 0.005551 0.088404 0.008462 0.000591

Bel7402-t/c 0.002158 0.456552 0.012585 0.000114

PLA801C-t/c 0.315335 0.98704 0.052304 0.737263

HepG2--PLA801C 0.832517 0.061966 0.003758 0.002493

Bel7402--PLA801C 0.949824 0.522942 0.026352 0.003916

HepG2--Bel7402 0.239669 0.216064 0.795694 0.280477

(P value＜0.05 is a significant difference)

3, RT-PCR detects the expression of E1a

With 1 * 10 ⁶Pfu AdhafE1 Δ 55 infects HepG2, Bel7402 and PLA801C respectively, hypoxia inducible (1%O ₂, 5%CO ₂And 94%N ₂, 37 ℃) to cultivate after 3 hours, collecting cell extracts cell total rna, detects the expression of E1a with RT-PCR.The result has detected the E1a cDNA that size is about 1000bp at liver cancer cell HepG2 and Bel7402, illustrate that AdhafE1 Δ 55 expressed E1a in HepG2 and Bel7402, and in PLA801C expression do not see Figure 14.This results suggest, the specific killing of 55 couples of human liver cancer cell HepG2 of observed AdhafE1 Δ and Be17402 is owing to this virus copy choice in HepG2 and Bel7402 cell causes in morphological observation and MTT biochemical test.

Sequence table

＜110〉Institute of Basic Medical Sciences, Academy of Military Medical Sciences, PLA

＜120〉a kind of hepatoma targeting character oncolytic adenovirus, Preparation Method And The Use

<130>

<160>14

<170>PatentIn?version?3.2

<210>1

<211>29

<212>DNA

<213>

<400>1

ctcaagctta?gctatgagtc?tgggcttgg 29

<210>2

<211>29

<212>DNA

<213>

<400>2

ctcggatcct?ttgggactgg?agttgcttc 29

<210>3

<211>31

<212>DNA

<213>

<400>3

ctcggatcct?ctgcaactta?gggacaagtc?a 31

<210>4

<211>28

<212>DNA

<213>

<400>4

ctcaagcttg?ttattggcag?tggtggaa 28

<210>5

<211>900

<212>DNA

<213>

<400>5

gtaatacgac?tcactatagg?gcgaattggg?cccacgtcgc?atgctcccgg?ccgccatggc 60

ggccgggaat?tcgattctca?agcttagcta?tgagtctggg?cttgggctga?tagaagcctt 120

ggcccctggc?ctggtgggag?ctctgggcag?ctggcctaca?gacgttcctt?agtgctggcg 180

ggtaggtttg?aatcatcacg?caggccctgg?acctccaccc?gcccccacca?gccccctggc 240

ctcagttccc?tggcaacatc?tggggttggg?ggggcagcag?gaacaagggc?ctctgtctgc 300

ccagctgcct?ccccctttgg?gttttgccag?actccacagt?gcatacgtgg?gctccaacag 360

gtcctcttcc?ctcccagtca?ctgactaacc?ccggaaccac?acagcttccc?gttctcagct 420

ccacaaactt?ggtgccaaat?tcttctcccc?tgggaagcat?ccctggacac?ttcccaaagg 480

accccagtca?ctccagcctg?ttggctgccg?ctcactttga?tgtcatttgt?tatatttgca 540

aaataaaata?agtttgcaag?tttttttttt?ctgccccaaa?gagctctgtg?tccttgaaca 600

taaaatacaa?ataaccgcta?tgctgttaat?tattggcaaa?tgtcccattt?tcaacctaag 660

gaaataccat?aaagtaacag?atataccaac?aaaaggttac?tagttaacag?gcattgcctg 720

aaaagagtat?aaaagaattt?cagcatgatt?ttccatattg?tgcttccacc?actgccaata 780

acgcatgcga?ggagaatcac?tagtgaattc?gcggccgcct?gcaggtcgac?catatgggag 840

agctcccaac?gcgttggatg?catagcttga?gtattctata?gtgtcaccta?aatagcttgg 900

<210>6

<211>30

<212>DNA

<213>

<400>6

ctcaggtacc?agctatgagt?ctgggcttgg 30

<210>7

<211>29

<212>DNA

<213>

<400>7

ctcactcgag?gttattggca?gtggtggaa 29

<210>8

<211>28

<212>DNA

<213>

<400>8

ctcactcgag?aaaatgagac?atattatc 28

<210>9

<211>22

<212>DNA

<213>

<400>9

ctcttatggc?ctggggcgtt?ta 22

<210>10

<211>29

<212>DNA

<213>

<400>10

ctcagatatc?tcaatctgta?tcttcatcg 29

<210>11

<211>30

<212>DNA

<213>

<400>11

ctcagatatc?ggatacagtt?cagccacctg 30

<210>12

<211>25

<212>DNA

<213>

<400>12

gaagtgaaat?ctgaataatt?ttgtg 25

<210>13

<211>22

<212>DNA

<213>

<400>13

caaaactaca?taggaccccc?ac 22

<210>14

<211>28

<212>DNA

<213>

<400>14

ctcgcatgcg?ttattggcag?tggtggaa 28

Claims (7)

1, a kind of hepatoma targeting character oncolytic adenovirus, it is characterized in that comprising the hepatoma targeting character hybrid promoter and the adenovirus E 1 district that are made of anoxic response element HRE and AFP core promoter AF0.3 and duplicate promotor gene, the downstream that promotor gene is positioned at the hepatoma targeting character hybrid promoter is duplicated in said adenovirus E 1 district.

2, adenovirus according to claim 1 is characterized in that said hepatoma targeting character hybrid promoter has the nucleotide sequence shown in the sequence 7 in the sequence table.

3, prepare the method for claim 1 or 2 described adenovirus, it is characterized in that may further comprise the steps:

(1) clone HRE and AF0.3 and structure hybrid promoter HREAF;

(2) make up adenovirus shuttle plasmid pShuttle-HREAF-E1 and pShuttle-HREAF-E1 Δ 55;

(3) produce recombination oncolytic adenovirus AdhafE1 Δ 55;

(4) the specific killing effect of 55 pairs of human liver cancer cells of AdhafE1 Δ.

4, method according to claim 3 is characterized in that cloning HRE and AF0.3 and makes up hybrid promoter HREAF and may further comprise the steps:

(1) the design primer carries out pcr amplification;

(2) make up plasmid pGEM-HRE and pGEM-AF0.3, and identify;

(3) structure of hybrid promoter HREAF.

5, method according to claim 3 is characterized in that making up adenovirus shuttle plasmid pShuttle-HREAF-E1 and pShuttle-HREAF-E1 Δ 55 may further comprise the steps:

(1) the design shuttle plasmid makes up required primer;

(2) preparation pShuttle-R;

(3) preparation pShuttle-HREAF;

(4) preparation pShuttle-HREAF-E1;

(5) preparation pShuttle-HREAF-E1 Δ 55.

6, method according to claim 3 is characterized in that producing recombination oncolytic adenovirus AdhafE1 Δ 55 and comprises the steps:

(1) the adenovirus shuttle plasmid linearizing that claim 5 is built prepares recombinant adenovirus plasmid through homologous recombination, and enzyme is cut the back transfectional cell, packs out purpose recombinant adenovirus particle;

(2) generation of recombinant adenovirus plasmid and evaluation in the bacterium

With the adenovirus shuttle plasmid linearizing that claim 5 builds, transformed competence colibacillus bacterium, dull and stereotyped recombinant plasmid pAdhafE1 and the pAdhafE1 Δ 55 selected of microbiotic;

(3) produce adenovirus in the mammalian cell

With recombinant plasmid amplification, purifying, enzyme is cut the back transfectional cell, packing recombinant adenovirus particle.

7, claim 1 or the 2 described recombinant adenovirus application in the preparation cancer treatment drug.

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