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组蛋白赖氨酸去甲基化酶及其在癌症中的功能。

Histone lysine demethylases and their functions in cancer.

作者信息

Sterling Jayden, Menezes Sharleen V, Abbassi Ramzi H, Munoz Lenka

机构信息

School of Medical Sciences and Charles Perkins Centre, Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.

出版信息

Int J Cancer. 2021 May 15;148(10):2375-2388. doi: 10.1002/ijc.33375. Epub 2020 Nov 19.

Abstract

Histone lysine demethylases (KDMs) are enzymes that remove the methylation marks on lysines in nucleosomes' histone tails. These changes in methylation marks regulate gene transcription during both development and malignant transformation. Depending on which lysine residue is targeted, the effect of a given KDM on gene transcription can be either activating or repressing, and KDMs can regulate the expression of both oncogenes and tumour suppressors. Thus, the functions of KDMs can be regarded as both oncogenic and tumour suppressive, contingent on cell context and the enzyme isoform. Finally, KDMs also demethylate nonhistone proteins and have a variety of demethylase-independent functions. These epigenetic and other mechanisms that KDMs control make them important regulators of malignant tumours. Here, we present an overview of eight KDM subfamilies, their most-studied lysine targets and selected recent data on their roles in cancer stem cells, tumour aggressiveness and drug tolerance.

摘要

组蛋白赖氨酸去甲基化酶(KDMs)是一类能够去除核小体组蛋白尾巴上赖氨酸甲基化标记的酶。这些甲基化标记的变化在发育和恶性转化过程中调节基因转录。根据靶向的赖氨酸残基不同,特定的KDM对基因转录的影响可能是激活或抑制,并且KDMs可以调节癌基因和肿瘤抑制因子的表达。因此,KDMs的功能可被视为具有致癌性和肿瘤抑制性,这取决于细胞背景和酶亚型。最后,KDMs还能使非组蛋白去甲基化,并具有多种不依赖于去甲基化酶的功能。KDMs所调控的这些表观遗传及其他机制使其成为恶性肿瘤的重要调节因子。在此,我们概述了八个KDM亚家族、它们研究最多的赖氨酸靶点以及有关它们在癌症干细胞、肿瘤侵袭性和药物耐受性中作用的最新数据。

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