Advanced prostate cancer is responsive to hormone therapy that interferes with androgen receptor (AR) signalling. However, the effect is short-lived, as nearly all tumours progress to a hormone-refractory (HR) state, a lethal stage of the disease. Intuitively, the AR should not be involved because hormone therapy that blocks or reduces AR activity is not effective in treating HR tumours. However, there is still a consensus that AR plays an essential role in HR prostate cancer (HRPC) because AR signalling is still functional in HR tumours. AR signalling can be activated in HR tumours through several mechanisms. First, activation of intracellular signal transduction pathways can sensitize the AR to castrate levels of androgens. Also, mutations in the AR can change AR ligand specificity, thereby allowing it to be activated by non-steroids or anti-androgens. Finally, overexpression of the wild-type AR sensitizes itself to low concentrations of androgens. Therefore, drugs targeting AR signalling could still be effective in treating HRPC.
机构:
Urologische Klinik, Charité, Universitätsmedizin, Berlin
Urologische Klinik, Charité, Universitätsmedizin, 12200 BerlinUrologische Klinik, Charité, Universitätsmedizin, Berlin
Miller K.
Börgermann C.
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Klinik und Poliklinik für Urologie, Universitätsklinikum, EssenUrologische Klinik, Charité, Universitätsmedizin, Berlin
Börgermann C.
Thüroff J.
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Urologische Klinik, Johannes-Gutenberg-Universität, MainzUrologische Klinik, Charité, Universitätsmedizin, Berlin
Thüroff J.
Albers P.
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Urologische Klinik, Universität, BonnUrologische Klinik, Charité, Universitätsmedizin, Berlin
Albers P.
Wirth M.
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Klinik und Poliklinik für Urologie, Universitätsklinikum Carl Gustav Carus, Technische Universität, DresdenUrologische Klinik, Charité, Universitätsmedizin, Berlin
机构:
Columbia Presbyterian Med Ctr, Genitourinary Oncol Program, New York, NY 10032 USAColumbia Presbyterian Med Ctr, Genitourinary Oncol Program, New York, NY 10032 USA