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增强子结合锌指蛋白 2:肿瘤治疗的潜在靶点。

Enhancer of zeste homolog 2: A potential target for tumor therapy.

机构信息

College of Life Sciences, Zhejiang University, 388 Yuhangtang Road, Hangzhou, Zhejiang Province, 310058, PR China.

出版信息

Int J Biochem Cell Biol. 2011 Apr;43(4):474-7. doi: 10.1016/j.biocel.2011.01.005. Epub 2011 Jan 15.

Abstract

Enhancer of zeste homolog 2 (EZH2) is a subunit of the Polycomb-Repressive Complex 2 (PRC2), which catalyses the trimethylation of histone H3 on Lys 27 (H3K27) and involves in genes repression. EZH2 is amplified and overexpressed in a variety of cancers, including prostate and breast cancer. Overexpression of EZH2 has been associated with the invasion and progression of malignant cancers, especially with the progression of prostate cancer. Here, we review the structure and biological function of EZH2, especially focused on its activities in the tumorigenesis.

摘要

增强子结合锌指蛋白 2(EZH2)是多梳抑制复合物 2(PRC2)的一个亚基,它催化组蛋白 H3 赖氨酸 27(H3K27)的三甲基化,并参与基因抑制。EZH2 在多种癌症中扩增和过表达,包括前列腺癌和乳腺癌。EZH2 的过表达与恶性肿瘤的侵袭和进展有关,特别是与前列腺癌的进展有关。在这里,我们回顾了 EZH2 的结构和生物学功能,特别是其在肿瘤发生中的活性。

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