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 language | English |
|---|---|
| Pages (from-to) | 1197-1205 |
| Number of pages | 9 |
| Journal | Urology |
| Volume | 79 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 2012 |
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