Nucleic acid and corresponding protein entitled 158P3D2 useful in treatment and detection of cancer
View Patent ↗A novel gene (designated 158P3D2) and its encoded protein, and variants thereof, are described wherein 158P3D2 exhibits tissue specific expression in normal adult tissue, and is aberrantly expressed in the cancers listed in Table I. Consequently, 158P3D2 provides a diagnostic, prognostic, prophylactic and/or therapeutic target for cancer. The 158P3D2 gene or fragment thereof, or its encoded protein, or variants thereof, or a fragment thereof, can be used to elicit a humoral or cellular immune response; antibodies or T cells reactive with 158P3D2 can be used in active or passive immunization.
1. A method of inhibiting growth of cancer cells, comprising:
administering to a cancer cell expressing a protein comprising the amino acid sequence of SEQ ID NO: 6275 an antibody or antigen binding fragment thereof that specifically binds to the protein, wherein the antibody or fragment thereof is conjugated to a cytotoxic agent selected from the group consisting of a radioactive isotope, a chemotherapeutic agent, and a toxin, and whereby the antibody or antigen binding fragment thereof binds to the protein on the cell, thereby inhibiting the growth of said cancer cell.
2. The method of claim 1 wherein said antibody is a single chain monoclonal antibody, or fragment thereof.
3. The method of claim 1 , wherein said antibody or fragment is a recombinant protein comprising the antigen-binding region of an antibody that specifically binds to 158P3D2 protein.
4. The method of claim 1 , wherein said antibody or fragment is a human antibody or fragment.
5. The method of claim 1 , wherein the cytotoxic agent is a radioactive isotope selected from the group consisting of 211 At, 131 I, 125 I, 90 Y, 186 Re, 188 Re, 153 Sm, 212 Bi and 32 P.
6. The method of claim 1 , wherein the cytotoxic agent is a chemotherapeutic agent selected from the group consisting of maytansinoids, yttrium, bismuth, doxorubicin, daunorubicin, taxol, ethidium bromide, mitomycin, etoposide, tenoposide, vincristine, vinblastine, and colchicine.
7. The method of claim 1 , wherein the cytotoxic agent is a toxin selected from the group consisting of dihydroxy anthracin dione, ricin, ricin A-chain, actinomycin, diphtheria toxin, Pseudomonas exotoxin (PE) A, PE40, abrin, abrin A chain, modeccin A chain, alpha-sarcin, gelonin, mitogellin, restrictocin, phenomycin, enomycin, curicin, crotin, calicheamicin, Saponaria officinalis inhibitor, and glucocorticoid.
8. The method of claim 1 , wherein the cancer cell is selected from the group of cancers consisting of prostate cancer, bladder cancer, kidney cancer, colon cancer, ovarian cancer, lung cancer, breast cancer, and pancreatic cancer.