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KMT2 基因在人类肿瘤中的作用。

The role of KMT2 gene in human tumors.

机构信息

Zhejiang Cancer Institute (Experimental Research Center), Zhejiang Cancer Hospital, Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou, PR China.

The Second Clinical Medical College of Zhejiang Chinese Medicine University, Hangzhou, PR China.

出版信息

Histol Histopathol. 2022 Apr;37(4):323-334. doi: 10.14670/HH-18-447. Epub 2022 Mar 2.

DOI:10.14670/HH-18-447
PMID:35233758
Abstract

Histone methylation plays a crucial role in the regulation of gene transcriptional expression, and aberration of methylation-modifying enzyme genes can lead to a variety of genetic diseases, including human cancers. The histone modified protein KMT2 (lysin methyltransferase) family are involved in cell proliferation, growth, development and differentiation through regulating gene expression, and are closely related with many blood cancers and solid tumors. In recent years, several studies have shown that mutations in the KMT2 gene occur frequently in a variety of human cancers and the mutation status of the KMT2 gene may be correlated with the occurrence, development and prognosis of some tumors. Research uncovering the clinical characteristics and molecular mechanisms of KMT2 mutation in human tumors will be helpful for early diagnosis and prognosis of tumors as well as drug development for targeted therapies.

摘要

组蛋白甲基化在基因转录表达的调控中起着至关重要的作用,甲基化修饰酶基因的异常会导致多种遗传疾病,包括人类癌症。组蛋白修饰蛋白 KMT2(赖氨酸甲基转移酶)家族通过调节基因表达参与细胞增殖、生长、发育和分化,与许多血液癌症和实体瘤密切相关。近年来,多项研究表明,KMT2 基因突变在多种人类癌症中频繁发生,KMT2 基因突变状态可能与某些肿瘤的发生、发展和预后相关。研究揭示 KMT2 基因突变在人类肿瘤中的临床特征和分子机制,有助于肿瘤的早期诊断和预后以及靶向治疗药物的开发。

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Clin Epigenetics. 2021 Aug 11;13(1):157. doi: 10.1186/s13148-021-01145-y.
2
O'Donnell-Luria-Rodan syndrome: description of a second multinational cohort and refinement of the phenotypic spectrum.O'Donnell-Luria-Rodan 综合征:第二个跨国队列的描述及表型谱的精细化。
J Med Genet. 2022 Jul;59(7):697-705. doi: 10.1136/jmedgenet-2020-107470. Epub 2021 Jul 28.
3
Chromatin state dynamics confers specific therapeutic strategies in enhancer subtypes of colorectal cancer.
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Gut. 2022 May;71(5):938-949. doi: 10.1136/gutjnl-2020-322835. Epub 2021 May 31.
4
Recruitment of KMT2C/MLL3 to DNA Damage Sites Mediates DNA Damage Responses and Regulates PARP Inhibitor Sensitivity in Cancer.KMT2C/MLL3 招募到 DNA 损伤部位介导 DNA 损伤反应,并调节癌症中 PARP 抑制剂的敏感性。
Cancer Res. 2021 Jun 15;81(12):3358-3373. doi: 10.1158/0008-5472.CAN-21-0688. Epub 2021 Apr 14.
5
Genomic alterations in KMT2 family predict outcome of immune checkpoint therapy in multiple cancers.KMT2 家族的基因组改变预测多种癌症免疫检查点治疗的结果。
J Hematol Oncol. 2021 Mar 2;14(1):39. doi: 10.1186/s13045-021-01050-0.
6
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