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前列腺癌中雄激素受体信号的表观遗传调控。

Epigenetic regulation of androgen receptor signaling in prostate cancer.

机构信息

Division of Hematology and Oncology, Knight Cancer Institute, Both at Oregon Health & Science University, Portland, OR, USA.

出版信息

Epigenetics. 2010 Feb 16;5(2):100-4. doi: 10.4161/epi.5.2.10778. Epub 2010 Feb 27.

Abstract

Prostate cancer is the most common cancer in men in the United States, and it is the second leading cause of cancer-related death in American men. The Androgen receptor (AR), a nuclear hormone and transcription factor, is the most therapeutically relevant target in this disease. While most efforts in the clinic are still directed at lowering levels of androgens that activate AR, resistance to androgen deprivation eventually develops, and most prostate cancer deaths are attributable to this castration-resistant form of this disease. Recent work has shed light on the importance of epigenetic events including facilitation of AR signaling by histone-modifying enzymes and also on the role that enzymes such as HDAC6 play in stabilizing AR in prostate cancer cells. Herein, we summarize recent findings on the role of epigenetic enzymes in AR signaling and highlight examples on how interdiction of critical epigenetic enzymes may attenuate AR action in prostate cancer.

摘要

前列腺癌是美国男性中最常见的癌症,也是美国男性癌症相关死亡的第二大主要原因。雄激素受体(AR)是一种核激素和转录因子,是该疾病最具治疗相关性的靶点。尽管临床上大多数努力仍致力于降低激活 AR 的雄激素水平,但雄激素剥夺的耐药性最终会发展,并且大多数前列腺癌死亡归因于这种去势抵抗形式的疾病。最近的研究揭示了表观遗传事件的重要性,包括组蛋白修饰酶促进 AR 信号转导,以及 HDAC6 等酶在稳定前列腺癌细胞中的 AR 中的作用。在此,我们总结了表观遗传酶在 AR 信号转导中的作用的最新发现,并强调了抑制关键表观遗传酶可能会减弱前列腺癌中 AR 作用的实例。

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