Li Zhongwei, Li Minle, Wang Diandian, Hou Pingfu, Chen Xintian, Chu Sufang, Chai Dafei, Zheng Junnian, Bai Jin
Cancer Institute, Xuzhou Medical University, 84 West Huaihai Road, Xuzhou, 221002, Jiangsu Province, China.
Center of Clinical Oncology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, 221002, Jiangsu Province, China.
Cell Biosci. 2020 Dec 11;10(1):143. doi: 10.1186/s13578-020-00505-0.
Enhancer of zeste homolog 2 (EZH2), as a main component of Polycomb Repressive Complex 2, catalyzes histone H3K27me3 to silence its target gene expression. EZH2 upregulation results in cancer development and poor prognosis of cancer patients. Post-translational modifications (PTMs) are important biological events in cancer progression. PTMs regulate protein conformation and diversity functions. Recently, mounting studies have demonstrated that EZH2 stability, histone methyltransferase activity, localization, and binding partners can be regulated by PTMs, including phosphorylation, O-GlcNAcylation, acetylation, methylation and ubiquitination. However, the detailed molecular mechanisms of the EZH2-PTMs and whether other types of PTMs occur in EZH2 remain largely unclear. This review presents an overview of different roles of EZH2 modification and EZH2-PTMs crosstalk during tumorigenesis and cancer metastasis. We also discussed the therapeutic potential of targeting EZH2 modifications for cancer therapy.
zeste同源物2增强子(EZH2)作为多梳抑制复合物2的主要成分,催化组蛋白H3K27me3以沉默其靶基因表达。EZH2上调导致癌症发展及癌症患者预后不良。翻译后修饰(PTMs)是癌症进展中的重要生物学事件。PTMs调节蛋白质构象和多样性功能。最近,越来越多的研究表明,EZH2的稳定性、组蛋白甲基转移酶活性、定位及结合伴侣可受PTMs调控,包括磷酸化、O-连接N-乙酰葡糖胺化、乙酰化、甲基化和泛素化。然而,EZH2-PTMs的详细分子机制以及EZH2是否存在其他类型的PTMs在很大程度上仍不清楚。本综述概述了EZH2修饰在肿瘤发生和癌症转移过程中的不同作用以及EZH2-PTMs的串扰。我们还讨论了靶向EZH2修饰用于癌症治疗的潜在治疗价值。