Prostate cancer: Re-focusing on androgen receptor signaling

被引:36
作者
Nieto, Maria
Finn, Stephen
Loda, Massimo
Hahn, William C.
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Broad Inst Harvard, Cambridge, MA 02142 USA
[3] MIT, Cambridge, MA 02142 USA
关键词
prostate cancer; androgen receptor;
D O I
10.1016/j.biocel.2007.01.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prostate cancer is the most common, non-dermatologic cancer in men. Since prostate cancer is highly associated with increased age, the incidence of this disease is expected to increase as the population ages. In its initial stages prostate cancer depends upon the actions of androgen, and androgen deprivation therapy induces tumor regression. Currently, androgen deprivation is achieved by either surgical or chemical androgen blockade. Unfortunately, nearly all prostate cancer patients develop tumors that grow despite androgen blockade and ultimately relapse. Many alterations in prostate cancer cells contribute to this state. Although chemotherapy induces short remissions in some patients, there are no curative therapies for metastatic disease. This review summarizes our current understanding in androgen signaling and the mechanisms that allow tumor cells to bypass androgen manipulation therapy. The identification of novel survival pathways and effector molecules that drive androgen independent growth is necessary to develop effective therapies for advanced prostate cancers. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1562 / 1568
页数:7
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