Selective estrogen receptor modulators for the chemoprevention of prostate cancer

  • Mitchell S Steiner

      Affiliations

    • Department of Urology, University of Tennessee, Memphis, Tennessee, USA (MSS, SR)
    • GTx, Inc., Memphis, Tennessee, USA (MSS)
    • Corresponding Author InformationReprint requests: Mitchell S. Steiner, MD, Department of Urology, University of Tennessee, Memphis, 1211 Union Avenue, Suite 340, Memphis, TN 38104
  • ,
  • Sharan Raghow

      Affiliations

    • Department of Urology, University of Tennessee, Memphis, Tennessee, USA (MSS, SR)
  • ,
  • Blake L Neubauer

      Affiliations

    • Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA (BLN)

Abstract 

The ability to interfere with prostate carcinogenesis, and as a consequence, prevent prostate cancer with drugs is the basis for chemoprevention. The prostate contains estrogen receptors in both the stroma and epithelium. Both animal models and human epidemiologic studies have implicated estrogens as an initiator of prostate cancer. In the aging male, prostate cancer occurs in an environment of rising estrogen and decreasing androgen levels. Selective estrogen receptor modulators (SERMs) have shown the ability to prevent (GTx-006 [acapodene]) and treat (GTx-006 and arzoxifene) prostate cancer, suggesting that they may be used in prostate cancer chemoprevention. A phase 2 clinical trial using GTx-006 for prostate cancer chemoprevention is currently being conducted.

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PII: S0090-4295(00)00944-4