EP1226150A1 - Tadg-15: une serine protease extracellulaire surexprimee dans des carcinomes - Google Patents

Tadg-15: une serine protease extracellulaire surexprimee dans des carcinomes

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Publication number
EP1226150A1
EP1226150A1 EP00973739A EP00973739A EP1226150A1 EP 1226150 A1 EP1226150 A1 EP 1226150A1 EP 00973739 A EP00973739 A EP 00973739A EP 00973739 A EP00973739 A EP 00973739A EP 1226150 A1 EP1226150 A1 EP 1226150A1
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European Patent Office
Prior art keywords
tadg
protein
dna
individual
fragment
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EP00973739A
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German (de)
English (en)
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EP1226150A4 (fr
Inventor
Timothy J. O'brien
Hirotoshi Tanimoto
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University of Arkansas
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University of Arkansas
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Priority claimed from US09/421,213 external-priority patent/US7022821B1/en
Application filed by University of Arkansas filed Critical University of Arkansas
Priority to EP07118615A priority Critical patent/EP1887082A3/fr
Publication of EP1226150A1 publication Critical patent/EP1226150A1/fr
Publication of EP1226150A4 publication Critical patent/EP1226150A4/fr
Withdrawn legal-status Critical Current

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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
    • C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
    • C12N9/6424—Serine endopeptidases (3.4.21)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • 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
    • 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
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
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    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844—Nucleic acid amplification reactions
    • C12Q1/6851—Quantitative amplification
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/136—Screening for pharmacological compounds

Definitions

  • TADG-15 AN EXTRACELLULAR SERINE PROTEASE OVEREXPRESSED IN CARCINOMAS
  • the present invention relates generally to the fields o f cellular biology and the diagnosis of neoplastic disease. More specifically, the present invention relates to an extracellular serine protease, termed tumor antigen-derived gene 15 (TADG- 15), which is overexpressed in carcinomas.
  • TADG- 15 tumor antigen-derived gene 15
  • Extracellular proteases have been directly associated with tumor growth, shedding of tumor cells and invasion of target organs. Individual classes of proteases are involved in, but n o t limited to, (a) digestion of stroma surrounding the initial tumor area, (b) digestion of the cellular adhesion molecules to allow dissociation of tumor cells; and (c) invasion of the basement membrane for metastatic growth and activation of both tu mor growth factors and angiogenic factors.
  • proteases mediate specific proteolysis and contribute to th e removal of extracellular matrix components surrounding tu mor cells, the digestion of intercellular adhesion molecules to allow dissociation of malignant cells and the activation of many growth and angiogenic factors . 1 3
  • proteases are classified into four families: serine proteases, metalloproteases, aspartic proteases and cysteine proteases . 3
  • the metalloproteases have been well studied in relation to tumor growth and progression, and they are known to be capable o f degrading the extracellular matrix, thereby enhancing th e invasive potential of malignant cells.
  • the prior art is deficient in the lack of effective means of screening to identify proteases overexpressed in carcinoma.
  • the present invention fulfills this longstanding need and desire in the art.
  • the present invention discloses a screening program to identify proteases overexpressed in carcinoma by examining PCR products amplified using differential display in early stage tumors and metastatic tumors compared to that of normal tissues.
  • the approach herein to identify candidate genes overexpressed in tumor cells has been to utilize the well conserved domains surrounding the triad of amino acids (His- Asp-Ser) prototypical of the catalytic domain of serine proteases .
  • His- Asp-Ser His- Asp-Ser
  • a PCR product pre sent only in carcinoma was subcloned and sequenced, and was found to have a catalytic domain which was consistent with the serine protease family. Reported herein is the complete cloning and sequencing of this transcript and evidence for its expression in ovarian tumor cells.
  • a DNA encoding a tumor antigen-derived gene (TADG- 15) protein selected from the following: (a) an isolated DNA which encodes a TADG-15 protein; (b) an isolated DNA which hybridizes under high stringency conditions to the isolated DNA of (a) above and which encodes a TADG-15 protein; and (c) a n isolated DNA differing from the isolated DNAs of (a) and ( b ) above in codon sequence due to the degeneracy of the genetic code, and which encodes a TADG-15 protein.
  • the embodiment further includes a vector comprising the TADG-15 DNA and regulatory elements necessary for expression of the DNA in a cell.
  • an isolated and purified TADG-15 protein coded for by DNA selected from the following: (a) an isolated DNA which encodes a TADG-15 protein; (b) an isolated DNA which hybridizes under high stringency conditions to isolated DNA o f (a) above and which encodes a TADG-15 protein; and (c) a n isolated DNA differing from the isolated DNAs of (a) and ( b ) above in codon sequence due to the degeneracy of the genetic code, and which encodes a TADG-15 protein.
  • a method for detecting TADG-15 mRNA in a sample comprising the steps of: (a) contacting a sample with a probe which is specific for TADG-15; and (b) detecting binding o f the probe to TADG-15 mRNA in the sample.
  • a kit for detecting TADG-15 mRNA comprising: an oligonucleotide probe specific for TADG-15. A label for detection is further embodied in the kit.
  • the present invention additionally embodies a method of detecting TADG-15 protein in a sample, comprising the steps of: (a) contacting a sample with an antibody which is specific for TADG-15 or a fragment thereof; and (b) detecting binding of th e antibody to TADG-15 protein in the sample.
  • th e present invention also embodies a kit for detecting TADG-15 protein, comprising: an antibody specific for TADG-15 protein o r a fragment thereof. Means for detection of the antibody is further embodied in the kit.
  • the present invention provides an antibody specific for the TADG-15 protein or a fragment thereof.
  • the present invention provides a method of screening for compounds that inhibit TADG-15, comprising the steps of: (a) contacting a sample comprising TADG-15 protein with a compound; and (b) assaying for TADG-15 protease activity.
  • a decrease in the TADG- 15 protease activity in the presence of the compound relative t o TADG-15 protease activity in the absence of the compound is indicative of a compound that inhibits TADG-15.
  • a method of inhibiting expression o f TADG-15 in a cell comprising the step of: (a) introducing a vector into a cell, whereupon expression of the vector produces TADG-15 antisense mRNA in the cell which hybridizes t o endogenous TADG-15 mRNA, thereby inhibiting expression of TADG-15 in the cell.
  • a method of inhibiting a TADG-15 protein in a cell comprising the step of: (a) introducing an antibody specific for a TADG-15 protein or a fragment thereof into a cell, whereupon binding of the antibody to the TADG-15 protein inhibits the TADG-15 protein.
  • a method of targeted therapy to an individual comprising the step of: (a) administering a compound containing a targeting moiety and a therapeutic moiety to an individual, wherein the targeting moiety is specific for TADG-15.
  • a method of diagnosing cancer in an individual comprising the steps of: (a) obtaining a biological sample from a n individual; and (b) detecting TADG-15 in the sample, wherein the presence of TADG-15 in the sample is indicative of the presence of carcinoma in the individual and the absence of TADG-15 in th e sample is indicative of the absence of carcinoma in the individual.
  • a method of vaccinating an individual against TADG-15 comprising the steps of: (a) inoculating an individual with a TADG-15 protein or fragment thereof that lacks TADG- 15 protease activity, wherein the inoculation with the TADG- 15 protein or fragment thereof elicits an immune response in th e individual, thereby vaccinating the individual against TADG-15.
  • a method of producing immune-activated cells directed toward TADG-15 comprising the steps of: exposing dendritic cells to a TADG-15 protein or fragment thereof that lacks TADG- 15 protease activity, wherein the exposure to said TADG-15 protein or fragment thereof activates the dendritic cells, thereby producing immune-activated cells directed toward TADG-15.
  • an immunogenic composition comprising a n immunogenic fragment of a TADG-15 protein and an appropriate adjuvant.
  • Figure 1 shows a comparison of the serine protease catalytic domain of TADG-15 with Hepsin (Heps, SEQ ID No. 3 ) , SCCE (SEQ ID No. 4), Trypsin (Try, SEQ ID No. 5), Chymotrypsin (Chymb, SEQ ID No. 6), Factor 7 (Fac7, SEQ ID No. 7) and Tissue plasminogen activator (Tpa, SEQ ID No. 8).
  • the asterisks indicate conserved amino acids of catalytic triad.
  • Figure 2 shows the nucleotide sequence of the TADG- 15 cDNA and the derived amino acid sequence of the TADG-15 protein.
  • the putative start codon is located at nucleotides 23 -25.
  • the potential transmembrane sequence is underlined. Possible N- linked glycosylation sites are indicated by a broken line.
  • the asterisks indicate conserved cysteine residues of CUB domain .
  • the SDE-motifs of the LDL receptor ligand binding repeat-like domain are boxed.
  • the arrow shows the arginine-valine b o nd cleaved upon activation.
  • the conserved amino acids of the catalytic triad; histidine, aspartic acid and serine residues are circled.
  • Figure 3 shows the amino acid sequence of the TADG- 15 protease, including functional sites and domains.
  • Figure 4 shows a diagram of the TADG-15 protein. 1 ; cytoplasmic domain, (aa #1-54), 2; transmembrane domain ( aa #55-57), 3; extracellular domain (aa #78-213), 4-5; CUB repeat (aa #214-447), 6-9; LDL receptor ligand binding repeat (class A motif) like domain (aa #453-602), 10; serine protease (aa #615 - 855 ) .
  • Figure 5 shows Northern blot analysis of TADG-15 mRNA expression in normal ovary, ovarian carcinomas, carcinoma cell lines, normal fetal tissues and normal adult tissues.
  • a single intense transcript of the TADG-15 was observed in every sub-type of carcinoma and the two ovarian carcinoma cell lines, SW626 and CAOV3, whereas no visible band was detected in normal ovary or the two breast cancer cell lines.
  • normal fetal tissues fetal kidney showed increased transcript and faint expression was detected in fetal lung.
  • the TADG-15 was detected in colon with low expression in small intestine and prostate.
  • Figure 6 A shows quantitative PCR analysis of TADG- 15 expression.
  • Expression levels of TADG-15 relative to ⁇ -tubulin are significantly elevated in all LMP tumors and carcinomas compared to that of normal ovaries, m; mucinous, s; serous .
  • Figure 6B shows the ratio of TADG-15 expression to expression of ⁇ -tubulin in normal ovary, LMP tumor and ovarian carcinoma.
  • TADG-15 mRNA expression levels were significantly elevated in both LMP tumor (*; p ⁇ 0.001) and carcinoma (**; p ⁇ 0.0001 ) compared to that in normal ovary. All 10 samples of normal ovary showed a low level of TADG-15 expression.
  • Figure 7 shows the TADG-15 expression in tumor cell lines derived from both ovarian and breast carcinoma tissues.
  • Figure 8 shows the overexpression of TADG-15 in other tumor tissues.
  • Figure 9 shows SW626 and CAOV3 cell lysates that were separated by SDS-PAGE and immunoblotted. Lanes 1 and 2 were probed with rabbit pre-immune serum as a negative control . Lanes 3 and 4 were probed with polyclonal rabbit antibody generated to a carboxy terminal peptide from TADG-15 protein sequence .
  • Figure 10 shows that immunohistochemical staining of normal ovarian epithelium ( Figure 10 A ) with a polyclonal antibody to a TADG-15 protease peptide shows no staining of th e stroma or epithelium.
  • antibody staining of carcinomas confirms the presence of TADG-15 expression in the cytoplasm of a serous low malignant potential tumor ( Figure 10B ) ; a mucinous low malignant potential tumor ( Figure 10C) ; a serous carcinoma ( Figure 10D); and its presence in both the cytoplasm and cell surface of an endometrioid carcinoma (Figure 10E).
  • Figure 11 shows an alignment of the human TADG 15 protein sequence with that of mouse epithin which demonstrates that the proteins are 84% similar and 81 % identical over 843 amino acids. Residues that are identical between the two proteins are indicated by a "-", while the "*" symbol represents th e
  • TADG15 translation termination The most significant difference between these two proteins lies in the carboxy-termini, which for epithin, includes 47 amino acids that are not present in TADG15.
  • Figure 12 shows a nucleotide sequence comparison between TADG-15 and human SNC-19 (GeneBank Accession No.
  • TADG-15 tumor antigen-derived gene 15
  • the TADG-15 cDNA is 3147 base pairs long (SEQ ID No. 1) encoding for a 855 amino acid protein (SEQ ID No. 2).
  • SEQ ID No. 2 The availability of the TADG-15 gene provides numerous utilities.
  • the TADG-15 gene can be used as a diagnostic o r therapeutic target in ovarian and other carcinomas, including breast, prostate, lung and colon.
  • the present invention is directed to DNA encoding a tumor antigen-derived gene (TADG-15) protein, selected from th e following: (a) an isolated DNA which encodes a TADG-15 protein ; (b) an isolated DNA which hybridizes under high stringency conditions to the isolated DNA of (a) above and which encodes a TADG-15 protein; and (c) an isolated DNA differing from th e isolated DNAs of (a) and (b) above in codon sequence due to th e degeneracy of the genetic code, and which encodes a TADG-15 protein. It is preferred that the DNA has the sequence shown in SEQ LD No. 1 and the TADG-15 protein has the amino acid sequence shown in SEQ ID No. 2.
  • the present invention is directed toward a vector comprising the TADG-15 DNA and regulatory elements necessary for expression of the DNA in a cell, or a vector in which the TADG-15 DNA is positioned in reverse orientation relative to the regulatory elements such that TADG-15 antisense mRNA is produced.
  • the DNA encodes a TADG-15 protein having the amino acid sequence shown in SEQ ID No. 2.
  • the invention is also directed toward host cells transfected with either of the above-described vector(s).
  • Representative host cells are bacterial cells, mammalian cells, plant cells and insect cells.
  • the bacterial cell is E. coli.
  • the present invention is directed toward an isolated and purified TADG-15 protein coded for by DNA selected from the following: (a) an isolated DNA which encodes a TADG- 15 protein; (b) an isolated DNA which hybridizes under high stringency conditions to isolated DNA of (a) above and which encodes a TADG-15 protein; and (c) an isolated DNA differing from the isolated DNAs of (a) and (b) above in codon sequence due to the degeneracy of the genetic code, and which encodes a TADG-15 protein.
  • the protein has the amino acid sequence shown in SEQ ID No. 2.
  • the present invention is directed toward a method for detecting TADG-15 mRNA in a sample, comprising the steps of: (a) contacting a sample with a probe which is specific for TADG- 15; and (b) detecting binding of the probe to TADG-15 mRNA in the sample.
  • the present invention is also directed toward a method of detecting TADG-15 protein in a sample, comprising the steps of: (a) contacting a sample with an antibody which is specific for TADG-15 or a fragment thereof; and (b) detecting binding of the antibody to TADG-15 protein in the sample.
  • the sample is a biological sample; preferably, the biological sample is from an individual; and typically, the individual is suspected of having cancer.
  • the present invention is directed toward a kit for detecting TADG-15 mRNA, comprising: an oligonucleotide probe , wherein the probe is specific for TADG-15.
  • the kit may further comprise: a label with which to label the probe; and means for detecting the label.
  • the present invention is additionally directed toward a kit for detecting TADG-15 protein, comprising: a n antibody which is specific for TADG-15 protein or a fragment thereof.
  • the kit may further comprise: means to detect the antibody.
  • the present invention is directed toward a antibody which is specific for TADG-15 protein or a fragment thereof.
  • the present invention is directed toward a method o f screening for compounds that inhibit TADG-15, comprising the steps of: (a) contacting a sample containing TADG-15 protein with a compound; and (b) assaying for TADG-15 protease activity.
  • a decrease in the TADG-15 protease activity in the presence of the compound relative to TADG-15 protease activity in the absence of the compound is indicative of a compound that inhibits TADG-15.
  • the present invention is directed toward a method o f inhibiting expression of TADG-15 in a cell, comprising the step of: (a) introducing a vector expressing TADG-15 antisense mRNA into a cell, which hybridizes to endogenous TADG-15 mRNA, thereby inhibiting expression of TADG-15 in the cell.
  • a vector expressing TADG-15 antisense mRNA into a cell, which hybridizes to endogenous TADG-15 mRNA, thereby inhibiting expression of TADG-15 in the cell.
  • th e inhibition of TADG-15 expression is for treating cancer.
  • the present invention is directed toward a method o f inhibiting a TADG-15 protein in a cell, comprising the step of: ( a ) introducing an antibody specific for a TADG-15 protein or a fragment thereof into a cell, which inhibits the TADG-15 protein.
  • the inhibition of the TADG-15 protein is for treating cancer.
  • the present invention is directed toward a method o f targeted therapy to an individual, comprising the step of: ( a ) administering a compound having a targeting moiety and a therapeutic moiety to an individual, wherein the targeting moiety is specific for TADG-15.
  • Representative targeting moiety are a n antibody specific for TADG-15 and a ligand or ligand binding domain (e.g., CUB, LDLR, protease and extracellular) that binds TADG-15.
  • a representative therapeutic moiety is a radioisotope, a toxin, a chemotherapeutic agent and immune stimulants.
  • the above-described method is useful when the individual suffers from ovarian cancer, breast cancer o r cancers of the prostate, lung, colon and cervix.
  • the present invention is directed toward a method of diagnosing cancer in an individual, comprising the steps of: ( a ) obtaining a biological sample from an individual; and ( b ) detecting TADG-15 in the sample.
  • the presence o f TADG-15 in the sample is indicative of the presence of carcinoma in the individual, and the absence of TADG-15 in the sample is indicative of the absence of carcinoma in the individual.
  • the biological sample is blood, ascites fluid, urine, tears, saliva or interstitial fluid.
  • Typical means of detecting TADG-15 are by Northern blot, Western blot, PCR, dot blot, ELIZA, radioimmunoassay, DNA chips or tumor cell labeling. This method may be useful in diagnosing cancers such as ovarian, breast and other cancers in which TADG-15 is overexpressed, such as lung, prostate and colon cancers.
  • the present invention is also directed to an antisense oligonucleotide having the nucleotide sequence complementary to a TADG-15 mRNA sequence.
  • the present invention is also directed to a composition comprising such an antisense oligonucleotide according and a physiologically acceptable carrier therefore.
  • the present invention is also directed to a method of treating a neoplastic state in an individual syndrome in an individual in need of such treatment, comprising the step of administering to said individual an effective dose of an antisense oligonucleotide of.
  • the neoplastic state is selected from the group consisting of from ovarian cancer, breast cancer, lung cancer, prostate cancer, colon cancer and other cancers in which TADG-15 is overexpressed.
  • th e oligonucleotides alone or in combination with other anti- neoplastic agents can be formulated for a variety of modes of administration, including systemic, topical or localized administration.
  • oligonucleotide active ingredient is generally combined with a pharamceutically accceptable carrier such as a diluent or excipient which can include fillers, extenders, binders , wetting agents, disintergrants, surface active agents or lubricants, depending on the nature of the mode of administration an d dosage forms.
  • a pharamceutically accceptable carrier such as a diluent or excipient which can include fillers, extenders, binders , wetting agents, disintergrants, surface active agents or lubricants, depending on the nature of the mode of administration an d dosage forms.
  • Typical dosage forms include tablets, powders , liquid preparations including suspensions, emulsions, and solutions, granules, capsules and suppositories, as well as liquid preparations for injections, including liposome preparations.
  • oligonucleotides of th e invention are formulated in liquid solutions, preferably in physiologically compatible buffers.
  • th e oligonucleotides can be formulated in solid form and redissolved or suspended immediately prior to use. Lyophilized forms are also incldued. Dosages that can be used for systemic administration preferably range from about 0.01 mg/kg to 5 0 mg/kg administered once or twice per day.
  • the present invention is directed toward a method o f vaccinating an individual against TADG-15 overexpression, comprising the steps of: (a) inoculating an individual with a TADG-15 protein or fragment thereof which lacks TADG-15 protease activity.
  • the inoculation with the TADG-15 protein o r fragment thereof elicits an immune response in the individual, thereby vaccinating the individual against TADG-15.
  • the vaccination with TADG-15 described herein is intended for a n individual who has cancer, is suspected of having cancer or is a t risk of getting cancer.
  • the TADG-15 fragment useful for vaccinating an individual are 9-residue fragments up to 20- residue fragments, with preferred 9-residue fragments shown in SEQ ID Nos. 2, 19, 20, 21, 29, 39, 49, 50, 59, 79, 80, 81, 82, 83 , 84, 89 and 90.
  • the present invention is directed toward a method o f producing immune-activated cells directed toward TADG-15, comprising the steps of: exposing dendritic cells to a TADG- 15 protein or fragment thereof that lacks TADG-15 protease activity, wherein exposure to the TADG-15 protein or fragment thereof activates the dendritic cells, thereby producing immune- activated cells directed toward TADG-15.
  • Representative immune-activated cells are B-cells, T-cells and dendrites.
  • the TADG- 15 fragment is a 9-residue fragment up to a 20-residue fragment, with preferable 9-residue fragments shown in SEQ ID Nos. 2, 1 9 , 20, 21, 29, 39, 49, 50, 59, 79, 80, 81, 82, 83, 84, 89 and 90.
  • the dendritic cells are isolated from an individual prior to exposure, and the activated dendritic cells reintroduced into the individual subsequent to exposure.
  • the individual for which this method may apply has cancer, is suspected of having cancer or is at risk of getting cancer.
  • the present invention is directed toward a n immunogenic composition, comprising an immunogenic fragment of a TADG-15 protein and an appropriate adjuvant.
  • the fragment is a 9-residue fragment up to a 20-residue fragment, with preferred 9-residue fragments shown in SEQ ID Nos. 2, 1 9 , 20, 21, 29, 39, 49, 50, 59, 79, 80, 81, 82, 83, 84, 89 and 90.
  • cDNA shall refer to th e DNA copy of the mRNA transcript of a gene.
  • derived amino acid sequence shall mean the amino acid sequence determined by reading the triplet sequence of nucleotide bases in the cDNA.
  • screening a library shall refer to the process of using a labeled probe to check whether, under the appropriate conditions, there is a sequence complementary to the probe present in a particular DNA library.
  • screening a library could be performed by PCR.
  • PCR refers to th e polymerase chain reaction that is the subject of U.S. Patent Nos. 4,683, 195 and 4,683,202 to Mullis, as well as o ther improvements now known in the art.
  • amino acid described herein are preferred to b e in the "L" isomeric form.
  • residues in the "D" isomeric form can be substituted for any L-amino acid residue, as long a s the desired functional property of immunoglobulin-binding is retained by the polypeptide.
  • NH 2 refers to the free amino group present at the amino terminus of a polypeptide.
  • COOH refers t o the free carboxy group present at the carboxy terminus of a polypeptide.
  • amino-acid residue sequences are represented herein by formulae whose left and right orientation is in the conventional direction of ami no - terminus to carboxy-terminus. Furthermore, it should be no ted that a dash at the beginning or end of an amino acid residue sequence indicates a peptide bond to a further sequence of o ne or more amino-acid residues.
  • a "replicon" is any genetic element (e.g., plasmid, chromosome, virus) that functions as an autonomous unit of DNA replication in vivo; i. e., capable of replication under its own control.
  • a “vector” is a replicon, such as plasmid, phage o r cosmid, to which another DNA segment may be attached so as t o bring about the replication of the attached segment.
  • a “vector” may further be defined as a replicable nucleic acid construct, e.g., a plasmid or viral nucleic acid.
  • a “DNA molecule” refers to the polymeric form o f deoxyribonucleotides (adenine, guanine, thymine, or cytosine) in its either single-stranded form or as a double-stranded helix.
  • This term refers only to the primary and secondary structure o f the molecule, and does not limit it to any particular tertiary forms.
  • this term includes double-stranded DNA found, inter alia, in linear DNA molecules (e.g., restriction fragments), viruses, plasmids, and chromosomes.
  • linear DNA molecules e.g., restriction fragments
  • viruses e.g., viruses, plasmids, and chromosomes.
  • the structure is discussed herein according to the normal convention of giving only the sequence in the 5' to 3' direction along the nontranscribed strand of DNA (i. e., the strand having a sequence homologous to the mRNA).
  • An expression vector is a replicable construct in which a nucleic acid sequence encoding a polypeptide is operably linked to suitable control sequences capable of effecting expression of the polypeptide in a cell.
  • control sequences include a transcriptional promoter and/or enhancer, suitable mRNA ribosomal binding sites, and sequences which control the termination of transcription and translation. Methods which are well known to those skilled in the art can be used to construct expression vectors containing appropriate transcriptional and translational control signals. See, for example, techniques described in Sambrook et al., 1989, Molecular Cloning: A Laboratory Manual (2nd Ed.), Cold Spring Harbor Press, N.Y.
  • a gene and its transcription control sequences are defined as being "operably linked” if the transcription control sequences effectively control transcription of the gene.
  • Vectors of th e invention include, but are not limited to, plasmid vectors and viral vectors.
  • Preferred viral vectors of the invention are tho se derived from retro viruses, adenovirus, adeno-associated virus, SV40 virus, or herpes viruses.
  • expression vectors contain promoter sequences which facilitate the efficient transcription of the inserted DNA fragment and are used in connection with the host.
  • the expression vector typically contains an origin of replication, promoter(s), terminator(s), a s well as specific genes which are capable of providing phenotypic selection in transformed cells.
  • the transformed hosts can b e fermented and cultured according to means known in the art t o achieve optimal cell growth.
  • An "origin of replication” refers to those DNA sequences that participate in DNA synthesis.
  • a DNA "coding sequence” is a double-stranded DNA sequence which is transcribed and translated into a polypeptide in vivo when placed under the control of appropriate regulatory sequences. The boundaries of the coding sequence are determined by a start codon at the 5' (amino) terminus and a translation stop codon at the 3' (carboxyl) terminus.
  • a coding sequence can include, but is not limited to, prokaryotic sequences, cDNA from eukaryotic mRNA, genomic DNA sequences from eukaryotic (e.g., mammalian) DNA, and even synthetic DNA sequences.
  • a polyadenylation signal an d transcription termination sequence will usually be located 3' t o the coding sequence.
  • Transcriptional and translational control sequences are DNA regulatory sequences, such as promoters, enhancers , polyadenylation signals, terminators, and the like, that provide for the expression of a coding sequence in a host cell.
  • a “promoter sequence” is a DNA regulatory region capable of binding RNA polymerase in a cell and initiating transcription of a downstream (3' direction) coding sequence .
  • the promoter sequence is bounded at its 3' terminus by the transcription initiation site and extends upstream (5' direction) to include the minimum number of bases or elements necessary to initiate transcription at levels detectable above background.
  • a transcription initiation site a s well as protein binding domains (consensus sequences) responsible for the binding of RNA polymerase.
  • Eukaryotic promoters often, but not always, contain "TATA" boxes and "CAT” boxes.
  • Prokaryotic promoters typically contain Shine-Dalgarno ribosome-binding sequences in addition to the -10 and - 35 consensus sequences.
  • An "expression control sequence” is a DNA sequence that controls and regulates the transcription and translation o f another DNA sequence.
  • a coding sequence is "under the control" of transcriptional and translational control sequences in a cell when RNA polymerase transcribes the coding sequence into mRNA, which is then translated into the protein encoded by th e coding sequence.
  • a "signal sequence” can be included near the coding sequence. This sequence encodes a signal peptide, N-terminal t o the polypeptide, that communicates to the host cell to direct th e polypeptide to the cell surface or secrete the polypeptide into th e media, and this signal peptide is clipped off by the host cell before the protein leaves the cell. Signal sequences can be found associated with a variety of proteins native to prokaryotes and eukaryotes .
  • the terms “restriction endonucleases” and “restriction enzymes” refer to enzymes, each of which cu t double-stranded DNA at or near a specific nucleotide sequence.
  • a cell has been "transformed” by exogenous o r heterologous DNA when such DNA has been introduced inside the cell.
  • the transforming DNA may or may not be integrated (covalently linked) into the genome of the cell.
  • the transforming DNA may be maintained on an episomal element such as a plasmid.
  • a stably transformed cell is o ne in which the transforming DNA has become integrated into a chromosome so that it is inherited by daughter cells throu gh chromosome replication.
  • This stability is demonstrated by th e ability of the eukaryotic cell to establish cell lines or clones comprised of a population of daughter cells containing the transforming DNA.
  • a "clone” is a population of cells derived from a single cell or ancestor by mitosis.
  • a "cell line” is a clone of a primary cell that is capable of stable growth in vitro for many generations.
  • Two DNA sequences are "substantially homologous" when at least about 75% (preferably at least about 80%, and mo st preferably at least about 90% or 95%) of the nucleotides match over the defined length of the DNA sequences. Sequences that are substantially homologous can be identified by comparing the sequences using standard software available in sequence data banks, or in a Southern hybridization experiment under, for example, stringent conditions as defined for that particular system. Defining appropriate hybridization conditions is within the skill of the art. See, e.g., Maniatis et al., supra; DNA Cloning, Vols. I & II, supra; Nucleic Acid Hybridization, supra.
  • a "heterologous" region of the DNA construct is a n identifiable segment of DNA within a larger DNA molecule that is not found in association with the larger molecule in nature .
  • the gene will usually be flanked by DNA that does not flank th e mammalian genomic DNA in the genome of the source organism.
  • coding sequence is a construct where the coding sequence itself is not found in nature (e.g., a cDNA where the genomic coding sequence contains introns, or synthetic sequences having codons different than the native gene). Allelic variations or naturally-occurring mutational events do not give rise to a heterologous region of DNA as defined herein.
  • the labels most commonly employed for these studies are radioactive elements, enzymes, chemicals which fluoresce when exposed to ultraviolet light, and others.
  • a number of fluorescent materials are known and can be utilized as labels. These include, for example, fluorescein, rhodamine, auramine, Texas Red, AMCA blue and Lucifer Yellow.
  • a particular detecting material is anti-rabbit antibody prepared in goats and conjugated with fluorescein through an isothiocyanate. Proteins can also b e labeled with a radioactive element or with an enzyme. The radioactive label can be detected by any of the currently available counting procedures.
  • the preferred isotope may be selected from 3H, 1 C, 3 2 P, ⁇ S, 36Q, 51 C r, 57 Co , 58 Co , 59 ⁇ 90 Y> 125 131T, and 186 Re.
  • Enzyme labels are likewise useful, and can be detected by any of the presently utilized colorimetric, spectrophotometric, fluorospectrophotometric, amperometric or gasometric techniques.
  • the enzyme is conjugated to the selected particle by reaction with bridging molecules such as carbodiimides, diisocyanates, glutaraldehyde and the like. Many enzymes which can be used in these procedures are known and can be utilized.
  • a particular assay system developed and utilized in the art is known as a receptor assay.
  • a receptor assay the material to be assayed is appropriately labeled and then certain cellular test colonies are inoculated with a quantitiy of both the label after which binding studies are conducted to determine th e extent to which the labeled material binds to the cell receptors . In this way, differences in affinity between materials can b e ascertained.
  • An assay useful in the art is known as a " cis/trans " assay.
  • this assay employs two genetic constructs, one o f which is typically a plasmid that continually expresses a particular receptor of interest when transfected into a n appropriate cell line, and the second of which is a plasmid that expresses a reporter such as luciferase, under the control of a receptor/ligand complex.
  • a reporter such as luciferase
  • the ligand will complex with the receptor, and the resulting complex will bind the response element and initiate transcription of the luciferase gene.
  • the resulting chemiluminescence is then measured photometrically, and dose response curves are obtained and compared to those of known ligands.
  • the term "host” is meant to include not only prokaryotes but also eukaryotes such as yeast, plant and animal cells.
  • a recombinant DNA molecule or gene which encodes a human TADG-15 protein of the present invention c an be used to transform a host using any of the techniques commonly known to those of ordinary skill in the art.
  • a vector containing coding sequences for the gene which encodes a human TADG-15 protein of the present invention for purposes of prokaryote transformation .
  • Prokaryotic hosts may include E. coli, S. tymphimurium, Serratia marcescens and Bacillus subtilis.
  • Eukaryotic hosts include yeasts such as Pichia pastoris, mammalian cells and insect cells.
  • the invention includes a substantially pure DNA encoding a TADG-15 protein, a DNA strand which will hybridize at high stringency to a probe containing a sequence of at least 1 5 consecutive nucleotides of (SEQ ID No. 1).
  • the protein encoded by the DNA of this invention may share at least 80% sequence identity (preferably 85%, more preferably 90%, and mo s t preferably 95%) with the amino acids listed in Figures 3 and 4 (SEQ ID No. 2). More preferably, the DNA includes the coding sequence of the nucleotides of Figure 2 (SEQ ID No. 1), or a degenerate variant of such a sequence.
  • This invention also includes a substantially pure DNA containing a sequence of a t least 15 consecutive nucleotides (preferably 20, more preferably 30, even more preferably 50, and most preferably all) of the region from nucleotides 1 to 3147 of the nucleotides shown in Figure 2 (SEQ ID No. 1).
  • substantially pure DNA DNA that is no t part of a milieu in which the DNA naturally occurs, by virtue o f separation (partial or total purification) of some or all of the molecules of that milieu, or by virtue of alteration of sequences that flank the claimed DNA.
  • the term therefore includes, for example, a recombinant DNA which is incorporated into a vector, into an autonomously replicating plasmid or virus, or into the genomic DNA of a prokaryote or eukaryote; or which exists as a separate molecule (e.g., a cDNA or a genomic or cDNA fragment produced by polymerase chain reaction (PCR) or restriction endonuclease digestion) independent of other sequences.
  • PCR polymerase chain reaction
  • a recombinant DNA which is part of a hybrid gene encoding additional polypeptide sequence, e.g., a fusion protein. Also included is a recombinant DNA which includes a portion o f the nucleotides listed in Figure 2 (SEQ ID No. 1) and which encodes an alternative splice variant of TADG-15.
  • a substantially pure protein is meant a protein which has been separated from at least some of tho se components which naturally accompany it. Typically, the protein is substantially pure when it is at least 60% (by weight) free from the proteins and other naturally-occurring organic molecules with which it is naturally associated in vivo.
  • the purity of the preparation is at least 75%, more preferably a t least 90%, and most preferably at least 99%.
  • a substantially p ure TADG-15 protein may be obtained, for example, by extraction from a natural source; by expression of a recombinant nucleic acid encoding a TADG-15 polypeptide; or by chemically synthesizing the protein. Purity can be measured by any appropriate method, e.g., column chromatography, such a s immunoaffinity chromatography using an antibody specific for TADG-15, poly aery lamide gel electrophoresis, or HPLC analysis.
  • a protein is substantially free of naturally associated components when it is separated from at least some of those contaminants which accompany it in its natural state.
  • a protein which is chemically synthesized or produced in a cellular system different from the cell from which it naturally originates will be, by definition, substantially free from its naturally associated components. Accordingly, substantially pure proteins include eukaryotic proteins synthesized in E. coli, other prokaryotes, o r any other organism in which they do not naturally occur.
  • oligonucleotide as used herein, is defined as a molecule comprised of two or more ribonucleotides, preferably more than three. Its exact size will depend upon many factors, which, in turn, depend upon the ultimate function and use of the oligonucleotide.
  • primer refers to an oligonucleotide, whether occurring naturally (as in a purified restriction digest) or produced synthetically, and which is capable of initiating synthesis of a strand complementary to a nucleic acid when placed under appropriate conditions, i. e., in the presence of nucleotides and an inducing agent, such as a DNA polymerase, and at a suitable temperature and pH.
  • the primer may be either single-stranded or double-stranded and must b e sufficiently long to prime the synthesis of the desired extension product in the presence of the inducing agent.
  • the exact length of the primer will depend upon many factors, including temperature, sequence and/or homology of primer and th e method used.
  • the oligonucleotide primer typically contains 15-25 or m ore nucleotides, depending upon the complexity of the target sequence, although it may contain fewer nucleotides.
  • the primers herein are selected to be "substanti" complementary to particular target DNA sequences. This me ans that the primers must be sufficiently complementary to hybridize with their respective strands. Therefore, the primer sequence need not reflect the exact sequence of the template. For example, a non-complementary nucleotide fragment (i. e., containing a restriction site) may be attached to the 5' end of the primer, with the remainder of the primer sequence being complementary t o the strand. Alternatively, non-complementary bases or longer sequences can be interspersed into the primer, provided that th e primer sequence has sufficient complementary with the sequence to hybridize therewith and form the template for synthesis of the extension product.
  • a non-complementary nucleotide fragment i. e., containing a restriction site
  • non-complementary bases or longer sequences can be interspersed into the primer, provided that th e primer sequence has sufficient complementary with the sequence to hybridize therewith and form the template for synthesis of the extension product.
  • the probe to which the DNA of the invention hybridizes preferably consists of a sequence of at least 2 0 consecutive nucleotides, more preferably 40 nucleotides, even more preferably 50 nucleotides, and most preferably 1 00 nucleotides or more (up to 100%) of the coding sequence of th e nucleotides listed in Figure 2 (SEQ ID No. 1) or the complement thereof.
  • Such a probe is useful for detecting expression of TADG- 15 in a cell by a method including the steps of (a) contacting mRNA obtained from the cell with a labeled TADG- 15 hybridization probe; and (b) detecting hybridization of the probe with the mRNA.
  • high stringency DNA hybridization and wash conditions characterized by high temperature and low salt concentration, e.g., wash conditions of 65°C at a salt concentration of approximately 0.1X SSC, or the functional equivalent thereof.
  • high stringency conditions may include hybridization at about 42°C in the presence of about 50 % formamide; a first wash at about 65°C with about 2X SSC containing 1 % SDS; followed by a second wash at about 65°C with about 0.1X SSC.
  • the DNA may have at least about 70% sequence identity to the coding sequence of the nucleotides listed in Figure 2 (SEQ ID No. 1), preferably at least 75% (e.g., at least 80%); and most preferably at least 90%.
  • the identity between two sequences is a direct function of the number of matching o r identical positions.
  • a position in both of the two sequences is occupied by the same monomeric subunit, e.g., if a given position is occupied by an adenine in each of two DNA molecules, then they are identical at that position.
  • the length of comparison sequences will generally be at least 50 nucleotides, preferably at least 60 nucleotides, more preferably at least 75 nucleotides, and most preferably 100 nucleotides.
  • Sequence identity is typically measured using sequence analysis software (e.g., Sequence Analysis Software Package of the Genetics Computer Group (GCG), University o f Wisconsin Biotechnology Center, 1710 University Avenue, Madison, Wl 53705).
  • the present invention comprises a vector comprising a DNA sequence which encodes a human TADG-15 protein, wherein said vector is capable of replication in a host, and comprises, in operable linkage: a) an origin of replication; b) a promoter; and c) a DNA sequence coding for said TADG-15 protein.
  • the vector of the present invention contains a portion of the DNA sequence shown in SEQ ID No. 1.
  • Vectors may be used to amplify and/or express nucleic acid encoding a TADG-15 protein or fragment thereof.
  • the invention also includes fragments (e.g., antigenic fragments) o f the TADG-15 protein (SEQ ID No. 2).
  • fragment as applied to a polypeptide, will ordinarily be at least 6 residues , more typically at least 9-12 residues, and preferably at least 1 3 - 20 residues in length, but less than the entire, intact sequence .
  • a fragment may be an individual domain of 20- 120 residues from SEQ ID No. 2.
  • Fragments of the TADG-15 protein can be generated by methods known to those skilled in the art, e.g., by enzymatic digestion of naturally occurring o r recombinant TADG-15 protein, by recombinant DNA techniques using an expression vector that encodes a defined fragment o f TADG-15, or by chemical synthesis.
  • TADG-15 The ability of a candidate fragment to exhibit a characteristic of TADG-15 (e.g., binding t o an antibody specific for TADG-15) can be assessed by methods described herein.
  • Purified TADG-15 or antigenic fragments o f TADG-15 can be used to generate new antibodies or to te s t existing antibodies (e.g., as positive controls in a diagnostic assay) by employing standard protocols known to those skilled in the art. Included in this invention is polyclonal antisera generated by using TADG-15 or a fragment of TADG-15 as the immunogen in, e.g., rabbits. Standard protocols for monoclonal and polyclonal antibody production known to those skilled in this art are employed. The monoclonal antibodies generated by this procedure can be screened for the ability to identify recombinant TADG-15 cDNA clones, and to distinguish them from other cDNA clones .
  • TADG- 15 proteins which are encoded, at least in part, by portions of SEQ ID No. 2, e.g., products of alternative mRNA splicing or alternative protein processing events, or in which a section of TADG- 15 sequence has been deleted.
  • the fragment, or the intact TADG-15 polypeptide may be covalently linked to another polypeptide, e.g., one which acts as a label, a ligand or a means to increase antigenicity.
  • the invention also includes a polyclonal o r monoclonal antibody which specifically binds to TADG-15.
  • the invention encompasses not only an intact monoclonal antibody, but also an immunologically-active antibody fragment, e.g., a Fab or (Fab) 2 fragment; an engineered single chain Fv molecule; or a chimeric molecule, e.g., an antibody which contains the binding specificity of one antibody, e.g., of murine origin, and th e remaining portions of another antibody, e.g., of human origin.
  • the antibody, or a fragment thereof may be linked to a toxin or to a detectable label, e.g., a radioactive label, non-radioactive isotopic label, fluorescent label, chemiluminescent label, paramagnetic label, enzyme label, or colorimetric label.
  • a detectable label e.g., a radioactive label, non-radioactive isotopic label, fluorescent label, chemiluminescent label, paramagnetic label, enzyme label, or colorimetric label.
  • suitable toxins include diphtheria toxin, Pseudomonas exotoxin A, ricin, and cholera toxin.
  • suitable enzyme labels include malate hydrogenase, staphylococcal nuclease, delta-5-steroid isomerase, alcohol dehydrogenase, alpha-glycerol phosphate dehydrogenase, triose phosphate isomerase, peroxidase, alkaline phosphatase, asparaginase, glucose oxidase, beta-galactosidase, ribonuclease, urease, catalase, glucose-6-phosphate dehydrogenase, glucoamylase, acetylcholinesterase, etc.
  • suitable radioisotopic labels include 3 H, 12S I, 131 I, 32 P, 5 S, 14 C, etc.
  • Paramagnetic isotopes for purposes of in vivo diagnosis can also be used according to the methods of this invention.
  • elements that are useful in magnetic resonance imaging.
  • fluorescent labels include a fluorescein label, an isothiocyalate label, a rhodamine label, a phycoerythrin label, a phycocyanin label, an allophycocyanin label, an ophthaldehyde label, a fluorescamine label, etc .
  • chemiluminescent labels include a luminal label, a n isoluminal label, an aromatic acridinium ester label, an imidazole label, an acridinium salt label, an oxalate ester label, a luciferin label, a luciferase label, an aequorin label, etc.
  • TADG-15 protein in a biological sample which includes the steps of contacting the sample with the labeled antibody, e.g., radioactively tagged antibody specific for TADG-15, and determining whether the antibody binds to a component of the sample.
  • Antibodies to the TADG-15 protein can be used in a n immunoassay to detect increased levels of TADG-15 protein expression in tissues suspected of neoplastic transformation . These same uses can be achieved with Northern blot assays and analyses .
  • the invention provides a number of diagnostic advantages and uses.
  • the TADG-15 protein is useful in diagnosing cancer in different tissues since this protein is highly overexpressed in tumor cells.
  • Antibodies (or antigen-binding fragments thereof) which bind to an epitope specific for TADG-15, are useful in a method of detecting TADG- 15 protein in a biological sample for diagnosis of cancerous o r neoplastic transformation.
  • This method includes the steps o f obtaining a biological sample (e.g., cells, blood, plasma, tissue, etc.) from a patient suspected of having cancer, contacting the sample with a labeled antibody (e.g., radioactively tagged antibody) specific for TADG-15, and detecting the TADG-15 protein using standard immunoassay techniques such as an ELISA.
  • a biological sample e.g., cells, blood, plasma, tissue, etc.
  • a labeled antibody e.g., radioactively tagged antibody
  • Antibody binding to the biological sample indicates that th e sample contains a component which specifically binds to a n epitope within TADG-15.
  • a standard Northern blot assay can be used to ascertain the relative amounts of TADG-15 mRNA in a cell o r tissue obtained from a patient suspected of having cancer, in accordance with conventional Northern hybridization techniques known to those of ordinary skill in the art.
  • This Northern assay uses a hybridization probe, e.g., radiolabelled TADG-15 cDNA, either containing the full-length, single stranded DNA having a sequence complementary to SEQ ID No. 1 ( Figure 2), or a fragment of that DNA sequence at least 20 (preferably at least 30 , more preferably at least 50, and most preferably at least 1 00 consecutive nucleotides in length).
  • the DNA hybridization probe can be labeled by any of the many different methods known t o those skilled in this art.
  • the specimen Upon patient hysterectomy, bilateral salpingo- oophorectomy, or surgical removal of neoplastic tissue, the specimen is retrieved and placed on ice. The specimen was then taken to the resident pathologist for isolation and identification of specific tissue samples. Finally, the sample was frozen in liquid nitrogen, logged into the laboratory record and stored at -80°C. Additional specimens were frequently obtained from the Cooperative Human Tissue Network (CHTN). These samples were prepared by the CHTN and shipped on dry ice. Upon arrival, these specimens (e.g., blood (serum), urine, saliva, tears and insterstitial fluid) were logged into the laboratory record and stored at -80°C.
  • CHTN Cooperative Human Tissue Network
  • CHTN Cooperative Human Tissue Network
  • ovarian tumors (10 low malignant potential tumors and 31 carcinomas) and 10 normal ovaries were obtained from surgical specimens and frozen in liquid nitrogen.
  • Messenger RNA (mRNA) isolation was performed according to the manufacturer's instructions using the Mini RiboSepTM Ultra mRNA Isolation Kit purchased from Becton Dickinson. In this procedure, polyA + mRNA was isolated directly from the tissue lysate using the affinity chromatography media oligo(dT) cellulose. The amount of mRNA recovered was quantitated by UV spectrophotometry.
  • cDNA First-strand complementary DNA
  • Promega T-vector plasmid and the ligation products used t o transform JM109 competent cells according to th e manufacturer's instructions (Promega). Positive colonies were cultured for amplification, the plasmid DNA isolated using the WizardTM Minipreps DNA purification system (Promega), and the plasmids were digested with Apal and Sacl restriction enzymes t o determine the size of the insert. Plasmids with inserts of the size(s) visualized by the previously described PCR product gel electrophoresis were sequenced. Individual colonies were cultured and plasmid DNA was isolated using the Wizard Miniprep DNA purification system (Promega). Applied Biosystems Model 373A DNA sequencing system was used for direct cDNA sequence determination .
  • sequencing reactions were carried out using PRISMTM Ready Reaction Dye DeoxyTM terminators (Applied Biosystems) according to the manufacturer's instructions. Residual dye terminators were removed from the completed sequencing reaction using a Centri-sepTM spin column (Princeton Separation) . Based upon the determined sequence, primers that specifically amplify the gene of interest were designed and synthesized.
  • the original TADG-15 subclone (436bp) was randomly labeled and used as a probe to screen an ovarian tumor cDNA library by standard hybridization techniques . 13
  • the library was constructed in 8ZAP using mRNA isolated from the tumor cells of a stage Ill/grade III ovarian adenocarcinoma patient. Three overlapping clones were obtained which spanned 3 147 nucleotides .
  • RNAs 10 ⁇ g mRNAs were size separated by electrophoresis through a 1% formaldehyde-agarose gel in 0.02 M MOPS, 0.05 M sodium acetate (pH 7.0), and 0.001 M EDTA. The mRNAs were then blotted to Hybond-N + nylon membrane (Amersham) by capillary action in 20x SSPE. The RNAs are fixed to the membrane by baking for 2 hours at 80°C. 32 P-labeled cDNA probes were made by Prime-a-Gene Labeling System (Promega). The PCR products amplified by the same primers described above were used for probes.
  • the blots were prehybridized for 30 min and hybridized for 60 min at 68°C with 32 P-labeled cDNA probe in ExpressHyb Hybridization Solution (CLONTECH). Control hybridization to determine relative gel loading was performed with a ⁇ -tubulin probe. Normal human tissues; spleen, thymus, prostate, testis, ovary, small intestine, colon and peripheral blood leukocyte, and normal human fetal tissues; brain, lung, liver and kidney (Human Multiple Tissue Northern Blot; CLONTECH) were also examined by the same hybridization procedure. Additional multiple tissue northern (MTN) blots from CLONTECH include the Human MTN blot, the Human MTN II blot, the Human Fetal MTN II blot, and the Human Brain MTN III blot.
  • MTN Multiple tissue northern
  • Polyclonal rabbit antibody was generated by immunization with a poly-lysine linked multiple Ag peptide derived from the TADG-15 protein sequence 'LFRDWIKENTGV' (SEQ ID No. 13). Approximately 20 ⁇ g of cell lysates were separated on a 15% SDS-PAGE gel and electroblotted to PVDF a t 100 V for 40 min at 4°C. The proteins were fixed to th e membrane by incubation in 50% MeOH for 10 min. The membrane was blocked overnight in TBS (pH 7.8) containing 0.2% non-fat milk. Primary antibody was added to the membrane at a dilution of 1 : 100 in 0.2% milk/TBS and incubated for 2 h a t room temperature.
  • the blot was washed and incubated with a 1 :3000 dilution of alkaline-phosphatase conjugated goat anti- rabbit IgG (BioRad) for 1 h at room temperature.
  • the blot was washed and incubated with a chemiluminescent substrate before a 10 sec exposure to X-ray film for visualization.
  • TADG-15 The mRNA overexpression of TADG-15 was determined using a quantitative PCR. Quantitative PCR was performed. 11 12 Oligonucleotide primers were used for TADG-15: forward 5'-ATGACAGAGGATTCAGGTAC-3' (SEQ ID No. 1 4 ) an d reverse 5'-GAAGGTGAAGTCATTGAAGA-3' (SEQ ID No. 15 ) ; and and for ⁇ -tubulin: forward 5'-CGCATCAACGTGTACTACAA-3' (SEQ ID No. 1 6 ) and reverse 5'-TACGAGCTGGTGGACTGAGA-3' (SEQ ID No. 17). ⁇ -tubulin was utilized as an internal control.
  • the PCR reaction mixture consists of cDNA derived from 50 ng of mRNA, 5 pmol of sense and antisense primers for both the TADG-15 gene and the ⁇ -tubulin gene, 200 ⁇ mol o f dNTPs, 5 ⁇ Ci of ⁇ - 32 PdCTP and 0.25 units of Taq DNA polymerase with reaction buffer (Promega) in a final volume of 25 ⁇ l.
  • the target sequences were amplified in parallel with the ⁇ -tubulin gene. Thirty cycles of PCR were carried out in a Thermal Cycler (Perkin Elmer Gene Amp 2400; Perkin-Elmer Cetus).
  • Each cycle of PCR included 30 sec of denaturation at 94°C, 30 sec of annealing at 60°C and 30 sec of extension at 72°C.
  • the annealing temperature varies according to the primers that are used in the PCR reaction. For the reactions involving degenerate primers, a n annealing temperature of 48°C was used. The appropriate annealing temperature for the TADG-15- and ⁇ -tubulin-specific primers is 62°C.
  • Immunohistochemical staining was performed using a Vectastain Elite ABC Kit (Vector). Formalin-fixed and paraffin- embedded specimens were routinely deparaffinized and processed using microwave heat treatment in 0.01 M sodium citrate buffer (pH 6.0). The specimens were incubated with normal goat serum in a moist chamber for 30 min. After incubation with biotinylated anti-rabbit IgG for 30 min, th e sections were then incubated with ABC reagent (Vector) for 3 0 min. The final products were visualized using the AEC substrate system (DAKO) and sections were counterstained with hematoxylin before mounting. Negative controls were performed using normal serum instead of the primary antibody.
  • DAKO AEC substrate system
  • TADG-15 is cloned and expressed in the opposite orientation such that an antisense RNA molecule (SEQ ID No. 1 8 ) is produced.
  • the antisense RNA is used to hybridize to the complementary RNA in the cell and thereby inhibit translation of TADG-15 RNA into protein.
  • a screening strategy to identify proteases which are overexpressed in human cancer has been developed in which RT- PCR products amplified specifically in tumors, as compared t o normal tissue, are examined. 9 During this effort, candidate genes were identified using redundant sense primers to the conserved amino acid histidine domain at the NH 3 end of the catalytic domain and antisense primers to the downstream conserved amino acid serine domain. Subcloning and sequencing th e appropriate 480 base pair band(s) amplified in such a PCR reaction provides the basis for identifying the gene(s) encoding proteases(s). Among these amplified catalytic domains, a new serine protease gene named TADG-15 (tumor antigen-derived gene 15) was identified. The catalytic domain of the newly identified TADG-15 protein is similar to other serine proteases and specifically contains conserved amino acids appropriate for the catalytic domain of the trypsin-like serine protease family.
  • the deduced open reading frame encoded by th e TADG-15 nucleotide sequence contains several distinct domains as follows: an amino terminal cytoplasmic tail (amino acids (aa) #1-54), a potential transmembrane domain (aa #55-77), an extracellular membrane domain (aa #78-213), two complement subcomponents Clr/Cls, Uegf, and bone morphogenetic protein 1 (CUB) repeats (aa #214- 447), four ligand binding repeats of the low density lipoprotein (LDL) receptor-like domain (aa #453-602) and a serine protease domain (aa #615-855).
  • amino acids amino acids
  • aa #55-77 potential transmembrane domain
  • aa #78-213 extracellular membrane domain
  • CRB bone morphogenetic protein 1
  • the TADG-15 protein also contains two potential N-linked glycosylation sites (aa #109 and 302) and a potential proteolytic cleavage site upstream from the protease domain (aa #614) which could release and/or activate the protease at the carboxy end of this protein.
  • TADG-15 contains an RGD motif (aa #249-251 ) which is commonly found in proteins involved in cell-cell adhesion.
  • transcript size for TADG-15 was determined to be approximately 3.2 kb and a single intense transcript appeared to be present in all of the carcinomas examined, whereas no visible band was detected in normal ovary ( Figure 5). This transcript size is also in good agreement with the sequence data predicting a transcript size of 3.15 kb.
  • the ovarian tumor cell lines, SW626 and CAOV3, also showed a n abundance of transcript, however little or no transcript was detectable in the breast carcinoma cell lines MDA-MB-231 and MDA-MB-4355.
  • TADG-15 was detected in colon with low levels o f expression in small intestine and prostate ( Figure 5).
  • TADG-15 transcripts were noted in all ovarian carcinomas, but were not present at detectable levels in any of the following tissues: a) normal ovary, b) fetal liver and brain, c) adult spleen, thymus, testes, ovary and peripheral blood lymphocytes, d) skeletal muscle, liver, brain o r heart. This evaluation was extended to a standard panel of about 40 tumors. Using TADG-15-specific primers, the expression was also examined in tumor cell lines derived from both ovarian and breast carcinoma tissues as shown in Figure 7 and in other tumor tissues as shown in Figure 8. Expression of TADG-15 was also observed in carcinomas of the breast, colon, prostate and lung.
  • Polyclonal antibodies developed to a synthetic peptide (a 12-mer) at the carboxy terminus of the protease domain were used to examine TADG-15 expression in cell lines by Western blot and by immunolocalization in normal ovary and ovarian tumors .
  • Western blots of cell extracts from SW626 and CAOV3 cells were probed with both antibody and preimmune sera ( Figure 9 ) .
  • Several bands were detected with the antibody, including bands of approximately 100,000 daltons, approximately 60,000 daltons and 32,000 daltons.
  • the anticipated molecular size of th e complete TADG-15 molecule is estimated to be approximately 100,000 daltons, and the protease domain which may be released by proteolytic cleavage at aa #614 is estimated to b e approximately 32,000 daltons. Some intermediate proteolytic product may be represented by the 60,000 dalton band.
  • Antibody staining of tumor cells confirms the presence of the TADG-15 protease in the cytoplasm of a serous LMP tumor, mucinous LMP tumor and serous carcinoma ( Figure 10B, C & D, respectively). This diffuse staining pattern may b e due to detection of TADG 15 within the cell as it is being packaged and transported to the cell surface.
  • Carcinoma 31 31 (100%) 0.771 ⁇ 0.380 serous 18 18 (100%) 0.779 ⁇ 0.332 mucinous 7 7 (100%) 0.907 ⁇ 0.584 endometrioid 3 3 (100%) 0.502 + 0.083 clear cell 3 3 ⁇ OO% 0.672 + 0.077
  • H-6201 clear cell carcinoma ++ H-5640 clear cell carcinoma ⁇
  • Epithin is a 902 amino acid protein which contains a similar structure to TADG-15 in that it has a cytoplasmic domain, transmembrane domain, two CUB domains, four LDLR-like domains and a carboxy terminal serine protease domain.
  • TADG-15 and epithin are 84% similar over 843 amino acids, suggesting that the proteins may b e orthologous ( Figure 11).
  • the precise role of epithin remains t o be elucidated.
  • a search of GeneBank for similar previously identified sequences yielded one such sequence with relatively high homology to a portion of the TADG-15 gene.
  • TADG-15 has a n open reading frame of 855 amino acids whereas the longest open reading frame of SNC-19 is 173 amino acids.
  • SNC- 19 does not include a proper start site for the initiation o f translation, nor does it include the amino terminal portion of th e protein encoded by TADG-15.
  • SNC-19 does n o t include an open reading frame for a functional serine protease because the His, Asp and Ser residues of the catalytic triad that are necessary for function are encoded in different reading frames .
  • the overall structure of the TADG-15 protein is relatively similar to the members of the tolloid/BMP-1 family and the complement subcomponents, Clr/Cls. These proteins contain both CUB and protease domains, and complex formation through the ligand binding domain is essential for their function. Activation of the serine protease domains of Clr and Cls requires proteolytic cleavage of Arg-Gly and Arg-Ile bonds, respectively. 1 5 Similarly, it might be expected that the TADG-15 protein is synthesized as a zymogen, which is activated by cleavage between Arg 614 and Val 615 and analogous to the activation mechanism of other serine protease zymogens.
  • CUB domains were first found in complement subcomponents C l r/C l s 16 18 and are known to be a widespread module in developmentally regulated proteins, such as the b one morphogenetic protein-1 (BMP-1) and the tolloid gene product. 18- 20 The role of these repeats remains largely unknown. However, some models suggest that the CUB domain may be involved in protein-protein interactions.
  • the CUB domain of Clr and Cls participates in the assembly of the Cls-Clr-Clr-Cls tetrameric complex in the activation of the classical pathway of complement by providing protein-protein interaction domains . 15
  • BMP-1 b one morphogenetic protein-1
  • Drosophila decapentaplegic (DPP) protein is essential for dorsal- ventral specification of the embryo, and the Drosophila tolloid (TLD) forms a complex with DPP to regulate its activity.
  • DPP Drosophila decapentaplegic
  • TLD Drosophila tolloid
  • the TADG-15 protein contains two tandem repeats o f CUB-like domains between amino acid residues 214 and 447. Each of these is approximately 110 amino acids long and each has four conserved cysteine residues characteristic of other CUBs (amino acids 214, 244, 268, 294, 340, 366, 397, 410).
  • the CUB repeats of the TADG-15 protein may form a n interactive domain capable of promoting multimeric complex formation and regulating the activity of the target protein o r TADG- 15 itself.
  • the TADG-15 protein also contains the LDL receptor ligand binding repeat (class A motif) -like domain, which consists of four contiguous cysteine-rich repeats (amino acid residues 453 to 602). Each cysteine-rich repeat is approximately 40 amino acids long and contains a conserved, negatively-charged sequence (Ser-Asp-Glu) with six cysteine residues. In the LDL receptor protein, this repeat is thought to function as a protein-binding domain which interacts with the lysine and arginine residues present in lipoproteins. 21 ,22 In addition, the first repeat of the LDL receptor appears to bind Ca 2+ and not the lipoproteins .
  • LDL receptor ligand binding repeat class A motif
  • LDL receptor-like repeat in TADG- 15 may act in a similar fashion, interacting with positively charged regions of other proteins and/or as a Ca 2+ binding site.
  • LDL receptor is internalized via clathrin-coated pits .
  • TADG-15 does not contain this motif in its cytosolic region, and furthermore, no similarities with other known protein sequences were found in the cytoplasmic domain of the TADG-15. This finding suggests th at TADG-15 functions in a different manner from the endocytic receptors (such as the LDL receptor), although TADG-15 possesses similar ligand-binding repeats in the extracellular matrix .
  • TADG-15 Although the precise role of TADG-15 is unknown, this gene is clearly overexpressed in ovarian tumors.
  • a variety o f proteases such as type IV collagenase and plasminogen activator, appear to be involved in the process of tumor invasion and are constituents of a protease cascade in malignant progression.
  • TADG-15 may constitute such an activity and directly digest extracellular matrix components surrounding a tumor, or activate other proteases by cleavage of inactive precursors, indirectly enhancing tumor growth and invasion. It is also possible that TADG-15 may function like a member of the tolloid/BMP-1 family by forming complexes with other growth factors or signal transduction proteins to modulate their activities.

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Abstract

Cette invention, qui a trait à un ADN codant une protéine TADG-15, porte également sur cette protéine TADG-15. Elle concerne, de plus, un vecteur, capable d'exprimer l'ADN selon l'invention, adapté pour une expression dans une cellule de recombinaison, ainsi que des éléments régulateurs nécessaires à l'expression de l'ADN dans la cellule. Cette invention porte, en outre, sur des méthodes permettant d'inhiber l'expression de la protéine TADG-15 et/ou l'activité de la protéase, sur des techniques de détection de l'ARN messager de la protéine TADG-15 ainsi que sur des méthodes de criblages d'inhibiteurs de la protéine TADG-15. Elle a trait, de surcroît, à un ciblage spécifique d'une cellule par le truchement de la protéine TADG-15 ainsi qu'à des méthodes de vaccination d'un individu contre la protéine TADG-15. Les méthodes décrites dans cette invention se révèlent des plus utiles en matière de diagnostic, de traitement et de prévention du cancer, notamment des cancers du sein et de l'ovaire.
EP00973739A 1999-10-20 2000-10-20 Tadg-15: une serine protease extracellulaire surexprimee dans des carcinomes Withdrawn EP1226150A4 (fr)

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US7795211B2 (en) * 2000-02-22 2010-09-14 Board Of Trustees Of The University Of Arkansas Methods for the early diagnosis of ovarian cancer
US7157596B2 (en) 2000-09-08 2007-01-02 Dendreon Corporation Inhibitors of serine protease activity of matriptase or MTSP1
US7019019B2 (en) 2002-12-23 2006-03-28 Dendreon Corporation Matriptase inhibitors and methods of use
ATE504602T1 (de) 2004-12-20 2011-04-15 Amgen Fremont Inc Für humane matriptase spezifische bindungsproteine
GB0611116D0 (en) * 2006-06-06 2006-07-19 Oxford Genome Sciences Uk Ltd Proteins
ES2550754T3 (es) 2007-08-07 2015-11-12 Oxford Biotherapeutics Ltd. Proteína matriptasa y usos de la misma
EP2427479B1 (fr) 2009-05-07 2018-11-21 The Regents of The University of California Anticorps et procédés d'utilisation de ceux-ci
US8455200B2 (en) 2009-10-15 2013-06-04 Traxxsson, Llc Measurement of PKA for cancer detection
CA2811000A1 (fr) 2010-09-09 2012-03-15 Traxxsson, Llc Procedes combines de diagnostic d'un cancer chez un patient
WO2014120555A1 (fr) 2013-01-31 2014-08-07 The Regents Of The University Of California Anticorps spécifiques pour l'activateur de plasminogène de type urokinase et procédés d'utilisation de ceux-ci
EP3074423A1 (fr) 2013-11-25 2016-10-05 Oxford BioTherapeutics Ltd Anticorps anti-matriptase pour le traitement du cancer
US9272027B1 (en) 2014-09-08 2016-03-01 The United States Of America As Represented By The Secretary Of The Air Force Francisella tularensis live vaccine strains and methods of use

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WO1998041656A1 (fr) * 1997-03-19 1998-09-24 The Board Of Trustees Of The University Of Arkansas Compositions et methodes pour le diagnostic precose du cancer ovarien
WO1999036550A2 (fr) * 1998-01-16 1999-07-22 Incyte Pharmaceuticals, Inc. Molecules de proteases humaines
WO1999042120A1 (fr) * 1998-02-20 1999-08-26 The Board Of Trustees Of The University Of Arkansas Serine protease extracellulaire surexprimee dans les cancers du sein ou les cancers ovariens

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WO2000042201A2 (fr) * 1999-01-11 2000-07-20 Incyte Pharmaceuticals, Inc. Peptidases humaines
JP4778617B2 (ja) * 1999-03-12 2011-09-21 ジョージタウン ユニバーシティ マトリプターゼ、セリンプロテアーゼおよびその応用

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Publication number Priority date Publication date Assignee Title
WO1998041656A1 (fr) * 1997-03-19 1998-09-24 The Board Of Trustees Of The University Of Arkansas Compositions et methodes pour le diagnostic precose du cancer ovarien
WO1999036550A2 (fr) * 1998-01-16 1999-07-22 Incyte Pharmaceuticals, Inc. Molecules de proteases humaines
WO1999042120A1 (fr) * 1998-02-20 1999-08-26 The Board Of Trustees Of The University Of Arkansas Serine protease extracellulaire surexprimee dans les cancers du sein ou les cancers ovariens

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* Cited by examiner, † Cited by third party
Title
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