CYP17 inhibitors for prostate cancer treatment – an update

V. M. Moreira, J. A. R. Salvador, T. S. Vasaitis, V. C. O. Njar

Research output: Contribution to journalReview article

37 Citations (Scopus)

Abstract

It is almost 70 years since the discovery by Huggins et al. that androgens are essential for prostate cancer (PC) growth and progression, and there has been about 30 years experience using ketoconazole for PC theraphy. Since then we have come a long way in learning about the disease and developing new strategies to approach it, among which is cytochrome 17alpha-hydroxylase-C17,20-lyase(CYP17) inhibition. This review focuses on the efforts to find prospective CYP17 inhibitors, both steroidal and nonsteroidal, in the absence of a 3D structure of the enzyme. It covers almost 4 decades of literature with highlights on the most significant achievements in this area, providing insight into PC pathophysiology, management and treatment options.
Original languageEnglish
Pages (from-to)868-899
Number of pages32
JournalCurrent Medicinal Chemistry
Volume15
Issue number9
DOIs
Publication statusPublished - 30 Apr 2008

Keywords

  • CYP17
  • prostate cancer
  • abiraterone
  • androgens
  • ketoconazole
  • nonsteroidal inhibitors
  • steroidal inhibitors

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