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. 2014 Dec;11(12):712-6.
doi: 10.1038/nrurol.2014.243. Epub 2014 Sep 16.

Emerging mechanisms of enzalutamide resistance in prostate cancer

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Emerging mechanisms of enzalutamide resistance in prostate cancer

Frank Claessens et al. Nat Rev Urol. 2014 Dec.

Abstract

The majority of prostate cancers are hormone-dependent at diagnosis highlighting the central role of androgen signalling in this disease. Surprisingly, most forms of castration-resistant prostate cancer (CRPC) are still dependent on the androgen receptor (AR) for survival. Therefore, the advent of new AR-targeting drugs, such as enzalutamide, is certainly beneficial for the many patients with metastatic CRPC. Indeed, this compound provides a substantial survival benefit-but it is not curative. This Perspectives article describes the different ways through which cancer cells can become resistant to enzalutamide, such as AR truncation and other mutations, as well as by-pass of the AR dependence of prostate cancer cells through expression of the glucocorticoid receptor. The clinical relevance of these mechanisms and emerging questions concerning new therapeutic regimens in the treatment of metastatic CRPC are being discussed.

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References

    1. Eur J Cancer. 2013 Dec;49(18):3821-30 - PubMed
    1. Cancer Res. 2013 Mar 1;73(5):1570-80 - PubMed
    1. Cancer Res. 2009 Mar 15;69(6):2305-13 - PubMed
    1. Eur Urol. 2014 Nov;66(5):815-25 - PubMed
    1. Nucl Recept Signal. 2008 Jun 27;6:e008 - PubMed

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