Yu Mengxue, Qian Kaiyu, Wang Gang, Xiao Yu, Zhu Yuan, Ju Lingao
Department of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, China.
Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Front Oncol. 2023 Mar 21;13:1114461. doi: 10.3389/fonc.2023.1114461. eCollection 2023.
SET domain-containing 2 (SETD2) is a lysine methyltransferase that catalyzes histone H3 lysine36 trimethylation (H3K36me3) and has been revealed to play important roles in the regulation of transcriptional elongation, RNA splicing, and DNA damage repair. mutations have been documented in several cancers, including clear cell renal cell carcinoma (ccRCC). deficiency is associated with cancer occurrence and progression by regulating autophagy flux, general metabolic activity, and replication fork speed. Therefore, SETD2 is considered a potential epigenetic therapeutic target and is the subject of ongoing research on cancer-related diagnosis and treatment. This review presents an overview of the molecular functions of SETD2 in H3K36me3 regulation and its relationship with ccRCC, providing a theoretical basis for subsequent antitumor therapy based on SETD2 or H3K36me3 targets.
含SET结构域蛋白2(SETD2)是一种赖氨酸甲基转移酶,可催化组蛋白H3赖氨酸36三甲基化(H3K36me3),并已被揭示在转录延伸、RNA剪接和DNA损伤修复的调控中发挥重要作用。在包括透明细胞肾细胞癌(ccRCC)在内的几种癌症中已记录到该基因的突变。SETD2缺陷通过调节自噬通量、一般代谢活性和复制叉速度与癌症的发生和进展相关。因此,SETD2被认为是一个潜在的表观遗传治疗靶点,并且是正在进行的癌症相关诊断和治疗研究的主题。本综述概述了SETD2在H3K36me3调控中的分子功能及其与ccRCC的关系,为后续基于SETD2或H3K36me3靶点的抗肿瘤治疗提供理论依据。