Development of a Second-Generation Antiandrogen for Treatment of Advanced Prostate Cancer

Author:

Tran Chris1,Ouk Samedy2,Clegg Nicola J.1,Chen Yu13,Watson Philip A.1,Arora Vivek1,Wongvipat John1,Smith-Jones Peter M.4,Yoo Dongwon2,Kwon Andrew1,Wasielewska Teresa1,Welsbie Derek5,Chen Charlie Degui5,Higano Celestia S.6,Beer Tomasz M.7,Hung David T.8,Scher Howard I.3,Jung Michael E.2,Sawyers Charles L.19

Affiliation:

1. Human Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

2. Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, CA 90095, USA.

3. Genitourinary Oncology Service, Division of Solid Tumor Oncology and Sidney Kimmel Center for Prostate and Urologic Cancers, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

4. Department of Radiology, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

5. Molecular Biology Institute, University of California Los Angeles, Los Angeles, CA 90095, USA.

6. Division of Oncology, Departments of Medicine and Urology, University of Washington, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.

7. OHSU Knight Cancer Institute, Oregon Health and Science University, Portland, OR 97239, USA.

8. Medivation, Inc., 201 Spear Street, San Francisco, CA 94105, USA.

9. Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

Abstract

A Second Act for Antiandrogens Men with advanced prostate cancer are often treated with antiandrogens; drugs that inhibit the activity of male hormones, such as testosterone, that help drive tumor growth. Many of these drugs act by functionally disrupting the androgen receptor (AR), a transcriptional regulator of cell proliferation, but tumors eventually become resistant to the drugs by expressing higher levels of the AR. Tran et al. (p. 787 , published online 9 April) have developed a “second-generation” antiandrogen, a thiohydantoin called MDV3100, which binds the AR with high affinity. MDV3100 retains its anticancer activity in cell culture and in mouse models even when AR levels are elevated. The drug appears to act both by inhibiting translocation of the AR into the nucleus and by reducing its transcriptional activity. MDV3100 is being tested in patients with advanced prostate cancer, the first group of which have shown a decline in blood levels of a marker of cancer growth, prostate-specific antigen.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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