TY - JOUR
T1 - Delineation of the androgen-regulated signaling pathways in prostate cancer facilitates the development of novel therapeutic approaches
AU - Awad, Dominik
AU - Pulliam, Thomas L.
AU - Lin, Chenchu
AU - Wilkenfeld, Sandi R.
AU - Frigo, Daniel E.
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/8
Y1 - 2018/8
N2 - Although androgen deprivation therapy (ADT) is initially effective for the treatment of progressive prostate cancer, it inevitably fails due to the onset of diverse resistance mechanisms that restore androgen receptor (AR) signaling. Thus, AR remains a desired therapeutic target even in the relapsed stages of the disease. Given the difficulties in stopping all AR reactivation mechanisms, we propose that the identification of the driver signaling events downstream of the receptor offer viable, alternative therapeutic targets. Here, we summarize recently described, AR-regulated processes that have been demonstrated to promote prostate cancer. By highlighting these signaling events and describing some of the ongoing efforts to pharmacologically modulate these pathways, our goal is to advocate potential new therapeutic targets that would represent an alternative approach for blocking AR actions.
AB - Although androgen deprivation therapy (ADT) is initially effective for the treatment of progressive prostate cancer, it inevitably fails due to the onset of diverse resistance mechanisms that restore androgen receptor (AR) signaling. Thus, AR remains a desired therapeutic target even in the relapsed stages of the disease. Given the difficulties in stopping all AR reactivation mechanisms, we propose that the identification of the driver signaling events downstream of the receptor offer viable, alternative therapeutic targets. Here, we summarize recently described, AR-regulated processes that have been demonstrated to promote prostate cancer. By highlighting these signaling events and describing some of the ongoing efforts to pharmacologically modulate these pathways, our goal is to advocate potential new therapeutic targets that would represent an alternative approach for blocking AR actions.
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U2 - 10.1016/j.coph.2018.03.002
DO - 10.1016/j.coph.2018.03.002
M3 - Review article
C2 - 29609138
AN - SCOPUS:85044600143
SN - 1471-4892
VL - 41
SP - 1
EP - 11
JO - Current Opinion in Pharmacology
JF - Current Opinion in Pharmacology
ER -