Claims
- 1. An antibody which neutralizes Cyr61 activity.
- 2. An antibody as defined in claim 1, which is chimeric.
- 3. An antibody as defined in claim 1, which is humanly acceptable.
- 4. An antibody as defined in claim 1, which is conjugated to an anti-tumor agent.
- 5. An antibody as defined in claim 1, which is a monoclonal antibody.
- 6. An antibody which binds to amino acids 163-229 or to amino acids 371-382 of SEQ ID NO:2.
- 7. An antibody which binds to one or more ligands of a sex steroid receptor which regulates the promoter of the gene which encodes Cyr61.
- 8. An antibody as defined in claim 7, wherein said sex steroid receptor is selected from the group consisting of estrogen receptor, progesterone receptor, and androgen receptor.
- 9. An oligonucleotide which binds under high stringency conditions to a polynucleotide encoding Cyr61.
- 10. An oligonucleotide as defined in claim 9, wherein said oligonulceotide is non-naturally occurring.
- 11. A vector comprising an oligonucleotide as defined in claim 9.
- 12. A pharmaceutical composition comprising a therapeutically effective amount of at least one of (i) an antibody as defined in any of claims 1-8; (ii) an oligonucleotide as defined in any of claims 8-9; or (iii) a vector as defined in claim 11.
- 13. A method for preventing or inhibiting breast cancer cell proliferation, said method comprising administering to a subject a breast cancer cell proliferation blocking or reducing amount of a Cyr61 neutralizing antibody.
- 14. A method as defined in claim 13, wherein said neutralizing antibody blocks sex steroid induced synthesis of Cyr61 DNA and proliferation of breast cancer cells.
- 15. A method as defined in claim 13, wherein said neutralizing antibody blocks growth factor induced synthesis of Cyr61 DNA and proliferation of breast cancer cells.
- 16. A method as defined in claim 15, wherein said growth factor is selected from the group consisting of epidermal growth factor, heparin binding epidermal growth factor, and basic fibroblastic growth factor.
- 17. A method for diagnosing or staging breast cancer, said method comprising determining the level of Cyr61 in a breast cancer cell present in said breast cancer suspected of being positive for breast cancer and comparing said level to the level of Cyr61 in normal breast tissue, whereby an increase in the level of Cyr61 in said suspect tissue over the level of Cyr61 in said normal tissue indicates the presence of breast cancer in said suspect tissue.
- 18. A method as defined in claim 17, wherein said level of Cyr61 is determined by exposing said suspect and said normal tissues to a Cyr61 neutralizing antibody and comparing the amount of antibody bound by each tissue, wherein an increase in the level of bound antibody by said suspect tissue over the level of bound antibody by said normal tissue indicates the presence of breast cancer in said suspect tissue.
- 19. A method for diagnosing or staging breast cancer, said method comprising determining whether breast tissue suspected of being positive for breast cancer is (i) ER/Cyr61 positive, (ii) PR/Cyr61 positive, (iii) ER/PR/Cyr61 positive, (iv) AR/Cyr61 positive, or (v) PR/EGFR/Cyr61 positive; whereby the presence of (i), (ii), (iii), (iv), or (v) indicates a likelihood that said suspect tissue is cancerous.
- 20. A method of screening for a compound which inhibits or prevents breast cancer cell proliferation, said method comprising determining a first amount of Cyr61 expressed by breast cancer cells exposed to said compound, wherein said breast cancer cells overexpress Cyr61; and comparing said first amount of Cyr61 to a second amount of Cyr61 expressed by said breast cancer cells that have not been exposed to said compound; whereby said first amount being less than said second amount indicates that said compound may inhibit or prevent breast cancer cell proliferation.
- 21. A method of screening for a compound which inhibits or prevents breast cancer cell proliferation, said method comprising determining whether said compound inhibits the interaction of sex steroid response element of the Cyr61 promoter and a sex steroid receptor associated with the Cyr61 promoter.
- 22. A method of screening for a compound which inhibits or prevents breast cancer cell proliferation, said method comprising determining whether said compound binds with a sex steroid receptor which regulates the Cyr61 promoter.
- 23. A transgenic non-human animal comprising DNA which can be induced to overexpress Cyr61 in breast tissue.
- 24. The transgenic non-human animal as defined in claim 23, wherein the DNA is human.
- 25. A kit for diagnosing or staging breast cancer, said kit comprising an antibody as defined in any of claims 1-8.
- 26. A kit for diagnosing or staging breast cancer, said kit comprising an oligonucleotide as defined in claim 9 or 10.
- 27. A method for screening compounds that regulate Cyr61 mRNA transcription through a receptor, said method comprising detecting a difference in the level of Cyr61 mRNA in a population of cells sufficient to transcribe a detectable amount of mRNA encoding Cyr61 contacted with a test compound in comparison with the level of Cyr61 mRNA in such a population that is not contacted with said test compound.
- 28. An assay method for detecting the presence of breast cancer, said method comprising detecting the level of Cyr61 mRNA isolated from breast cancer tissue, in comparison with the level of Cyr61 mRNA isolated from normal mammary tissue; wherein an upregulation of Cyr61 mRNA compared to normal mammary tissue indicates the presence of breast cancer.
- 29. An assay method for detecting the presence of breast cancer, said method comprising detecting the level of Cyr61 protein isolated from breast cancer tissue, in comparison with the level of Cyr61 protein isolated from normal mammary tissue; wherein an upregulation of Cyr61 protein compared to normal mammary tissue indicates the presence of breast cancer.
- 30. A method for preventing or inhibiting breast cancer cell proliferation, said method comprising administering to a subject, an amount of a compound effective to inhibit the interaction of a sex steroid receptor with a sex steroid response element of the Cyr61 promoter.
- 31. A method as defined in claim 15, wherein said sex steroid is selected from the group consisting of an estrogenic compound, a progestational compound, and an androgenic compound.
- 32. A method as defined in claim 13 or 18, wherein said neutralizing antibody is an antibody of claims 1-8.
- 33. A method as defined in claim 22, 23 or 30, wherein said steroid receptor is selected from the group consisting of estrogen receptor, progesterone receptor, and androgen receptor.
- 34. The method as defined in claim 31, wherein said estrogenic compound is 17β-estradiol
- 35. An antibody which binds to an epitope of Cyr61.
PRIORITY
[0001] The present application claims priority from U.S. Provisional Patent Application Serial No. 60/213,182, filed Jun. 21, 200, and U.S. Provisional Patent Application Serial No. 60/291,510, filed May 16, 2001, which are hereby incorporated by reference in their entireties.
PCT Information
Filing Document |
Filing Date |
Country |
Kind |
PCT/US01/19823 |
6/21/2001 |
WO |
|