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赖氨酸特异性去甲基化酶1A引发的致癌活性机制。

Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A.

作者信息

Yang Chao, Li Dan, Zang Shaohong, Zhang Lei, Zhong Zhangfeng, Zhou Yingtang

机构信息

National Engineering Research Center for Marine Aquaculture, Institute of Innovation and Application, Zhejiang Ocean University, Zhoushan, China.

State Key Laboratory of Southwestern Chinese Medicine Resource, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Front Pharmacol. 2022 Jul 19;13:955218. doi: 10.3389/fphar.2022.955218. eCollection 2022.

Abstract

Epigenetics has emerged as a prime focus area in the field of cancer research. Lysine-specific demethylase 1A (LSD1), the first discovered histone demethylase, is mainly responsible for catalysing demethylation of histone 3 lysine 4 (H3K4) and H3K9 to activate or inhibit gene transcription. LSD1 is abnormally expressed in various cancers and participates in cancer proliferation, apoptosis, metastasis, invasion, drug resistance and other processes by interacting with regulatory factors. Therefore, it may serve as a potential therapeutic target for cancer. This review summarises the major oncogenic mechanisms mediated by LSD1 and provides a reference for developing novel and efficient anticancer strategies targeting LSD1.

摘要

表观遗传学已成为癌症研究领域的一个主要重点领域。赖氨酸特异性去甲基化酶1A(LSD1)是首个被发现的组蛋白去甲基化酶,主要负责催化组蛋白3赖氨酸4(H3K4)和H3K9的去甲基化,以激活或抑制基因转录。LSD1在多种癌症中异常表达,并通过与调节因子相互作用参与癌症增殖、凋亡、转移、侵袭、耐药等过程。因此,它可能成为癌症的潜在治疗靶点。本文综述了LSD1介导的主要致癌机制,为开发针对LSD1的新型高效抗癌策略提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d9/9428822/e0c4d30ea28d/fphar-13-955218-g001.jpg

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