实用肿瘤学杂志 ›› 2022, Vol. 36 ›› Issue (6): 551-555.doi: 10.11904/j.issn.1002-3070.2022.06.011

• 综述 • 上一篇    下一篇

m6A RNA甲基化修饰影响恶性肿瘤及肿瘤干细胞生物学特性的研究进展

王馨艺, 路一平(综述), 孙峥嵘(审校)   

  1. 中国医科大学附属盛京医院生物样本库(沈阳 110000)
  • 收稿日期:2022-03-30 修回日期:2022-10-18 出版日期:2022-12-28 发布日期:2023-01-06
  • 通讯作者: 孙峥嵘,E-mail:sunzr@sj-hospital.org
  • 作者简介:王馨艺,女,(1997-),硕士研究生,从事HPV相关疾病及机制的研究
  • 基金资助:
    国家自然科学基金(编号:82000076)

Research progress on the effects of m6A RNA methylation modification on the biological characteristics of malignant tumors and tumor stem cells

WANG Xinyi, LU Yiping, SUN Zhengrong   

  1. Biobank of Shengjing Hospital Affiliated to China Medical University,Shenyang 110000,China
  • Received:2022-03-30 Revised:2022-10-18 Online:2022-12-28 Published:2023-01-06

摘要: N6-甲基腺苷(N6-methyladenosine,m6A)甲基化是在甲基转移酶、去甲基转移酶、m6A特有蛋白—YT521-B同源(YT521-B homology,YTH)结构家族、胰岛素样生长因子2(Insulin-like growth factor 2,IGF2BPs)以及核不均一核糖蛋白(Heterogeneous nuclear ribonucleoproteins,HNRNPs)等共同参与调节下的动态可逆反应,是目前研究最多的RNA转录前修饰。基础和临床方面的研究发现,在多种修饰酶与肿瘤基因的相互作用下,m6A甲基化修饰不仅影响肿瘤的发生,同时也可以调节肿瘤干细胞的增殖和分化,从而促进恶性肿瘤的发展及远处转移。因此深入研究m6A甲基化修饰,有助于明确恶性肿瘤的发生机制并进一步完善恶性肿瘤的治疗策略。

关键词: N6-甲基腺苷, 肿瘤细胞, 肿瘤干细胞

Abstract: N6-methyladenosine(m6A)methylation is a dynamic reversible reaction under the co-regulation of methyltransferase,demethyltransferase,the m6A-specific protein-YT521-B homology(YTH)structure family,insulin-like growth factor 2(IGF2BPs)and heterogeneous nuclear ribonucleoproteins(HNRNPs).It is currently the most studied as RNA pre-transcriptional modifications.Basic and clinical studies have found that under the interaction between various modifying enzymes and tumor genes,m6A methylation modification not only affects the occurrence of tumors,but also regulates the proliferation and differentiation of cancer stem cells,thereby promoting the development and distant metastasis of malignant tumors.Therefore,further study of m6A methylation modification will help to clarify the pathogenesis of malignant tumors and further improve the treatment strategy of malignant tumors.

Key words: N6-methyladenosine, Tumor cells, Cancer stem cells

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