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Prostate Cancer Chemoprevention

5α-Reductase Inhibitors
  • Jennifer E. Drisko
  • Siu-Long Yao
Chapter
Part of the Cancer Drug Discovery and Development book series (CDD&D)

Abstract

5α-reductase is a nuclear membrane-bound NADPH-dependent δ-3-ketosteroid 5α-oxidoreductase. It is found in androgen-sensitive tissues, and catalyzes the conversion of testosterone to dihydrotestosterone (DHT). Two known isoenzymes of 5α-reductase have been identified: Type 1 predominates in peripheral tissues such as the skin and liver, and Type 2 is predominant in the prostate. Finasteride is a specific inhibitor of the Type 2 isoenzyme, and effectively blocks the Type 2-mediated conversion of testosterone to DHT, but does not inhibit the binding of DHT to the androgen receptor (AR) (1).

Keywords

Prostate Cancer Benign Prostatic Hyperplasia Radical Prostatectomy Prostate Specific Antigen Level Prostate Cancer Prevention Trial 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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© Springer Science+Business Media New York 2004

Authors and Affiliations

  • Jennifer E. Drisko
  • Siu-Long Yao

There are no affiliations available

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