Finasteride metabolism and pharmacogenetics: New approaches to personalized prevention of prostate cancer

Sarah L. Hulin-Curtis, Dominique Petit, W. Douglas Figg, Ann W. Hsing, Juergen Kv Reichardt

Research output: Contribution to journalReview articlepeer-review

14 Scopus citations

Abstract

Incidences of prostate cancer in most countries are increasing owing to better detection methods; however, prevention with the use of finasteride, a very effective steroid 5α-reductase type II inhibitor, has been met with mixed success. A wide interindividual variation in response exists and is thought to be due to heritable factors. This article summarizes the literature that attempts to elucidate the molecular mechanisms of finasteride in terms of its metabolism, excretion and interaction with endogenous steroid molecules. We describe previously reported genetic variations of steroid-metabolizing genes and their potential association with finasteride efficacy. Based on the literature, we outline directions of research that may contribute to understanding the interindividual variation in finasteride prevention and to the future development of personalized medicine.

Original languageEnglish
Pages (from-to)1897-1913
Number of pages17
JournalFuture Oncology
Volume6
Issue number12
DOIs
StatePublished - Dec 2010
Externally publishedYes

Keywords

  • CYP3A4
  • SRD5A2
  • UGT1A
  • androgen
  • finasteride
  • haplotype
  • personalized medicine
  • pharmacogenetics
  • prostate cancer
  • single nucleotide polymorphism

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