Department of Urology, Case Western Reserve University, Cleveland, OH, USA.
Epigenetics. 2013 May;8(5):464-76. doi: 10.4161/epi.24532. Epub 2013 Apr 17.
Overexpression of EZH2 and other PRC2 subunits, such as SUZ12, is associated with tumor progression and poor prognosis in several human malignancies. Nevertheless, the underlying mechanisms driving aberrant EZH2 expression are poorly understood. This review provides molecular insights into the essential role of EZH2 in breast and prostate tumorigenesis. We addressed the current understanding on the oncogenic role of EZH2, with an emphasis on: (1) the less known PRC2-independent role of EZH2 in gene activation, in addition to its canonical role in transcriptional silencing as a histone methyltransferase catalyzing the trimethylation of histone H3 at lysine 27; (2) causes and consequences of its deregulation in tumor cells and; (3) collaboration of EZH2 with other epigenetic and hormone receptor-mediated oncogenic signaling pathways. We also summarize how EZH2 has emerged as a promising therapeutic target in hormone-refractory cancers and the prospects for integrating EZH2 blockade with available pharmacological inhibitors.
EZH2 和其他 PRC2 亚基(如 SUZ12)的过表达与几种人类恶性肿瘤的肿瘤进展和预后不良有关。然而,驱动异常 EZH2 表达的潜在机制仍知之甚少。本综述提供了 EZH2 在乳腺癌和前列腺肿瘤发生中的关键作用的分子见解。我们探讨了 EZH2 的致癌作用的现有认识,重点关注:(1)EZH2 在基因激活中的鲜为人知的 PRC2 非依赖性作用,除了其作为组蛋白甲基转移酶催化组蛋白 H3 赖氨酸 27 三甲基化的转录沉默的经典作用;(2)EZH2 在肿瘤细胞中的失调的原因和后果;(3)EZH2 与其他表观遗传和激素受体介导的致癌信号通路的协作。我们还总结了 EZH2 如何成为激素难治性癌症中很有前途的治疗靶点,以及将 EZH2 阻断与现有的药理学抑制剂相结合的前景。