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探索EZH2的致癌作用及临床意义:聚焦于非经典活性

Exploring oncogenic roles and clinical significance of EZH2: focus on non-canonical activities.

作者信息

Wozniak Michal, Czyz Malgorzata

机构信息

Department of Molecular Biology of Cancer, Medical University of Lodz, Lodz, Poland.

Department of Molecular Biology of Cancer, Medical University of Lodz, Mazowiecka 6/8, Lodz 92-215, Poland.

出版信息

Ther Adv Med Oncol. 2025 Jan 7;17:17588359241306026. doi: 10.1177/17588359241306026. eCollection 2025.

Abstract

The enhancer of zeste homolog 2 (EZH2) is a catalytic component of Polycomb repressive complex 2 (PRC2) mediating the methylation of histone 3 lysine 27 (H3K27me3) and hence the epigenetic repression of target genes, known as canonical function. Growing evidence indicates that EZH2 has non-canonical roles that are exerted as PRC2-dependent and PRC2-independent methylation of non-histone proteins, and methyltransferase-independent interactions of EZH2 with various proteins contributing to gene expression regulation and alterations in the protein stability. is frequently mutated and/or its expression is deregulated in various cancer types. The cancer sensitivity to inhibitors of EZH2 enzymatic activity and state-of-the-art approaches to deplete EZH2 with chemical degraders are discussed. This review also presents the clinical trials in various phases that evaluate the use of EZH2 inhibitors, both as monotherapy and in combination with other agents for the treatment of patients with diverse types of cancers.

摘要

zeste 同源物 2(EZH2)增强子是多梳抑制复合物 2(PRC2)的催化成分,介导组蛋白 3 赖氨酸 27(H3K27me3)的甲基化,从而对靶基因进行表观遗传抑制,这被称为经典功能。越来越多的证据表明,EZH2 具有非经典作用,这些作用通过对非组蛋白的 PRC2 依赖性和 PRC2 非依赖性甲基化,以及 EZH2 与各种蛋白质的甲基转移酶非依赖性相互作用来发挥,这些相互作用有助于基因表达调控和蛋白质稳定性改变。EZH2 在多种癌症类型中经常发生突变和/或其表达失调。本文讨论了癌症对 EZH2 酶活性抑制剂的敏感性以及使用化学降解剂耗尽 EZH2 的最新方法。本综述还介绍了评估 EZH2 抑制剂作为单一疗法以及与其他药物联合用于治疗不同类型癌症患者的各阶段临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aa1/11705335/2850ac804bce/10.1177_17588359241306026-fig1.jpg

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