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Role of 5 alpha-reductase inhibitors in the treatment of advanced prostatic carcinoma.

Abstract
Everything we know about the biology of the prostate supports the concept that DHT is the obligate androgen responsible for normal and hyperplastic growth. Whether this selectivity is maintained during malignant transformation is unknown. The consistent emergence of androgen-insensitive disease highlights the spectrum of biologic evolution this cancer is capable of. If the tumor is dependent only on DHT for neoplastic growth, the unique characteristics of a 5 alpha-reductase inhibitor offer several potential actions that warrant a systematic evaluation.
AuthorsG J Gormley
JournalThe Urologic clinics of North America (Urol Clin North Am) Vol. 18 Issue 1 Pg. 93-8 (Feb 1991) ISSN: 0094-0143 [Print] United States
PMID1846988 (Publication Type: Journal Article, Review)
Chemical References
  • 5-alpha Reductase Inhibitors
  • Androgens
  • Androstenes
  • Azasteroids
  • Finasteride
Topics
  • 5-alpha Reductase Inhibitors
  • Androgens (physiology)
  • Androstenes (therapeutic use)
  • Animals
  • Azasteroids (therapeutic use)
  • Finasteride
  • Humans
  • Male
  • Prostate (physiology)
  • Prostatic Neoplasms (drug therapy, physiopathology)

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