Key targets of hormonal treatment of prostate cancer. Part 2: the androgen receptor and 5 alpha-reductase

AN (André) Vis, Fritz Schröder

Research output: Contribution to journalArticleAcademicpeer-review

27 Citations (Scopus)


OBJECTIVE The inhibition of 5 alpha-reductase (5AR) blocks the synthesis of the most powerful intracellular androgen, dihydrotestosterone (DHT). The prostate has two 5AR isoenzymes (5AR1 and 5AR2) that change in expression and cellular location during the development of prostate cancer and tumour progression. The objective of this review is to provide an understanding of the pharmacological properties and the potential clinical benefits of 5AR inhibition. METHODS We searched Pubmed for data obtained from pharmacological, preclinical and clinical studies. RESULTS 5AR1 expression increases with increasing aggressiveness and extension of malignant prostatic disease. Conversely, 5AR2 expression decreases from benign prostatic tissue to localized prostate cancer. The efficacy of 5AR2 monotherapy with finasteride alone or in combination with an androgen receptor antagonist on more final outcome measures seems to be limited. Combining an androgen receptor antagonist with a 5AR inhibitor in patients with asymptomatic, locally advanced or recurrent prostate cancer might be a reasonable first therapeutic hormonal approach. As plasma testosterone levels are maintained, beneficial effects on quality of life, potency and sexual function are expected. From studies on the dual 5AR inhibitor dutasteride, the drug produces a biochemical response in some men who progressed under androgen-deprivation therapy, and is generally well tolerated. CONCLUSIONS Achieving more potent suppression of intracellular DHT synthesis by 5AR inhibition is expected to provide clinical benefit to patients. Previous studies have shown that 5AR inhibition, by dutasteride in particular, halts/delays the progression of disease, and might even cause regression of disease in patients with advanced prostate cancer.
Original languageUndefined/Unknown
Pages (from-to)1191-1197
Number of pages7
JournalBJU International
Issue number9
Publication statusPublished - 2009

Research programs

  • EMC MM-03-49-01

Cite this