Development of a quantitative RT‐PCR method to study 5α‐reductase mRNA isozymes in rat prostate in different androgen status

Publisher Website
Google Scholar
Abstract
BACKGROUND: The incidence of prostate cancer (PCa) and benign prostatic hypertrophy (BPH) continues to rise in the Western world. The development and growth of the prostate gland depends on androgen stimulation. Dihydrotestosterone (DHT) is the primary androgen responsible for prostate development and also for the pathogenesis of benign prostatic hyperplasia (BPH). DHT is synthesized in prostate from circulating testosterone (T) through the action of 5α‐Reductase (5α‐R) (EC 1.3.99.5), which occurs as two isozymes, type‐1 and type‐2. Both types are expressed in the prostate: type‐2 isozyme is predominantly expressed in prostate and is implicated in BPH and PCa; type‐1 isozyme is also increased in some prostatic adenocarcinomas. In recent years, various inhibitors of type‐2 isozyme or of both type‐1 and type‐2 isozyme have been used in prostatic diseases.METHODS: We present the first published measurements of mRNA levels of steroid 5α‐R isozymes in the ventral prostate of rats of different androgen status. We used a novel method that combines the high specificity of competitive PCR with the sensitivity of laser‐induced capillary electrophoresis (LIF‐CE).RESULTS: We demonstrated that T and DHT androgens control the expression of both 5α‐R isozymes in rat prostrate.CONCLUSIONS: This approach could be of great value for the study of prostate diseases in humans and would allow study at the transcriptional level of the effects of drugs that inhibit either or both of these isozymes. Prostate 56: 74–79, 2003.