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靶向组蛋白 H3 赖氨酸 36 甲基转移酶治疗癌症的最新进展。

Recent advances in targeting histone H3 lysine 36 methyltransferases for cancer therapy.

机构信息

Jiangsu Key Laboratory of Drug Design and Optimization and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, China.

Department of Medicinal Chemistry, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.

出版信息

Eur J Med Chem. 2024 Aug 5;274:116532. doi: 10.1016/j.ejmech.2024.116532. Epub 2024 May 23.

Abstract

Histone H3 lysine 36 (H3K36) methylation is a typical epigenetic histone modification that is involved in various biological processes such as DNA transcription, repair and recombination in vivo. Mutations, translocations, and aberrant gene expression associated with H3K36 methyltransferases have been implicated in different malignancies such as acute myeloid leukemia, lung cancer, multiple myeloma, and others. Herein, we provided a comprehensive overview of the latest advances in small molecule inhibitors targeting H3K36 methyltransferases. We analyzed the structures and biological functions of the H3K36 methyltransferases family members. Additionally, we discussed the potential directions for future development of inhibitors targeting H3K36 methyltransferases.

摘要

组蛋白 H3 赖氨酸 36(H3K36)甲基化是一种典型的表观遗传组蛋白修饰,参与体内多种生物学过程,如 DNA 转录、修复和重组。与 H3K36 甲基转移酶相关的突变、易位和异常基因表达与不同的恶性肿瘤有关,如急性髓系白血病、肺癌、多发性骨髓瘤等。本文全面概述了针对 H3K36 甲基转移酶的小分子抑制剂的最新进展。我们分析了 H3K36 甲基转移酶家族成员的结构和生物学功能。此外,我们还讨论了针对 H3K36 甲基转移酶抑制剂的未来发展的潜在方向。

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