Use of arginine vasopressin receptor antagonists for the treatment of prostate cancer
Described herein are methods of decreasing the proliferation of prostate cancer cells in a mammalian subject by administering to a subject in need thereof a composition comprising an AVPR antagonist in amount effective to decrease proliferation of the cancer cells. Also provided are methods of inducing prostate cancer cell death (or decreasing invasion migration of the prostate cancer cells) in a mammalian subject by administering to a subject in need thereof a composition comprising an AVPR antagonist.
1. A method of treating metastatic prostate cancer in a mammalian subject consisting of administering a composition consisting of an arginine vasopressin receptor (AVPR) 1a antagonist that selectively inhibits AVPR1a and not AVPR1b or AVPR2 to a mammalian subject having an AVRP1a-expressing prostate cancer in an amount effective to treat the metastatic prostate cancer.
2. The method of claim 1 , wherein the AVPR1a antagonist is selected from the group consisting of a small molecule, an antibody, a peptide antagonist and an oligonucleotide antagonist.
3. The method of claim 1 , wherein the AVPR1a antagonist is selected from the group consisting of Relcovaptan, OPC-21268, PF-00738245, SRX-251, SRX-246, Conivaptan, Nelivaptan, Lixivaptan, Mozavaptan, Satavaptan, Tolvaptan and demeclocycline.
4. The method of claim 1 , wherein the AVPR1a antagonist is Relcovaptan.
5. A method of decreasing the proliferation or metastasis of prostate cancer cells in a mammalian subject having metastatic prostate cancer, consisting of contacting the cells with a composition consisting of an arginine vasopressin receptor (AVPR) 1a antagonist that selectively inhibits AVPR1a and not AVPR1b or AVPR2 to in an amount effective to decrease proliferation or metastasis of the cancer cells in the subject.
6. The method of 5 , wherein the AVPR1a antagonist is selected from the group consisting of a small molecule, an antibody, a peptide antagonist and an oligonucleotide antagonist.
7. The method of claim 5 , wherein the AVPR1a antagonist is selected from the group consisting of Relcovaptan, OPC-21268, PF-00738245, SRX-25 and SRX-246.
8. The method of claim 7 , wherein the AVPR1a antagonist is Relcovaptan.
9. A method of treating metastatic prostate cancer in a mammalian subject consisting of administering a composition consisting of an arginine vasopressin receptor (AVPR) 1a antagonist that selectively inhibits AVPR1a and not AVPR1b or AVPR2 to a mammalian subject having an AVRP1a-expressing prostate cancer in an amount effective to treat the metastatic prostate cancer; and a composition consisting of a therapeutic selected from the group consisting of an androgen receptor antagonist, an inhibitor of androgen synthesis, a gonadotropin-releasing hormone (GnRH) agonist and a GnRH antagonist.
10. The method of claim 9 , wherein the androgen receptor antagonist is selected from the group consisting of Enzalutamide, Bicalutamide, Ostarine, Flutamide, Cyproterone acetate, Gugguisterone, Nilutamide, PF998245, (R)-Bicalutamide, 1,1-Dichloro-2,2-bis(4-chlorophenyl)ethene, ARN-509 and MDV-3100.
11. The method of claim 9 , wherein the inhibitor of androgen synthesis is Abiraterone acetate.
12. The method of claim 9 , wherein the GnRH agonist is selected from the group consisting of leuprolide, buserelin, histrelin, goserelin and deslorelin.
13. The method of claim 9 , wherein the GnRH antagonist is selected from the group consisting of cetrorelix, ganirelix, abarelix and degarelix.