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Role of 5α-reductase inhibitors in prostate cancer prevention and treatment

  • Roswell Park Cancer Institute

Research output: Contribution to journalReview articlepeer-review

37 Scopus citations

Abstract

Although testosterone is the most abundant serum androgen, dihydrotestosterone is the main prostatic androgen. Testosterone is converted to dihydrotestosterone by the enzyme 5α-reductase (5α-R). Dihydrotestosterone plays an important role in several human diseases, including benign prostate enlargement and prostate cancer. The observation that males born with 5α-R 2 deficiency have never been reported to develop prostate cancer stimulated interest in development of 5α-R inhibitors. Thus far, 2 5α-R inhibitors are approved for clinical use. Several trials evaluated the use of 5α-R inhibitors in prostate cancer prevention and treatment and will be reviewed in this article.

Original languageEnglish
Pages (from-to)1197-1205
Number of pages9
JournalUrology
Volume79
Issue number6
DOIs
StatePublished - Jun 2012

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