Accepted Preprint (first posted online 17 March 2014)

    Androgen receptor antagonists for prostate cancer therapy

    1. Frank Claessens
    1. C Helsen, Cellular and Molecular Medicine, KU Leuven, Leuven, 3000, Belgium
    2. T Van den Broeck, Development and Regeneration, University Hospitals Leuven, Leuven, Belgium
    3. A Voet, Center for Life Science Technologies, RIKEN, Yokohama, Japan
    4. S Prekovic, Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium
    5. H Van Poppel, Development and Regeneration, University Hospitals Leuven, Leuven, Belgium
    6. S Joniau, Development and Regeneration, University Hospitals Leuven, Leuven, Belgium
    7. F Claessens, Molecular Cell Biology, KU Leuven, Leuven, 3000, Belgium
    1. Correspondence: Christine Helsen, Email: Christine.helsen{at}med.kuleuven.be

    Abstract

    Androgen deprivation is the mainstay therapy for metastatic prostate cancer. Another way of suppressing androgen receptor signaling is via AR antagonists or antiandrogens. Despite being frequently prescribed in clinical practice, there is conflicting evidence concerning the role of AR antagonists in the management of prostate cancer. In the castrate resistant settings of prostate cancer, docetaxel has been the only treatment option for decades. With recent evidence that castrate resistant prostate cancer is far from AR-independent, there has been an increasing interest in developing new AR antagonists. This review gives a concise overview of the clinically available antiandrogens and the experimental AR antagonists that tackle androgen action with a different approach.

    • Received 18 December 2013
    • Revision received 21 February 2014
    • Accepted 13 March 2014
    • Accepted Preprint first posted online on 17 March 2014

    This Article

    1. Endocr Relat Cancer ERC-13-0545
    1. Abstract
    2. All Versions of this Article:
      1. ERC-13-0545v1
      2. 21/4/T105 most recent