实用肿瘤学杂志 ›› 2024, Vol. 38 ›› Issue (6): 421-426.doi: 10.11904/j.issn.1002-3070.2024.06.011

• 综述 • 上一篇    

RNA甲基化在肺癌中的研究进展

陈星燕1, 李雪1 综述, 付强2 审校   

  1. 1.黑龙江中医药大学研究生院(哈尔滨 150040);
    2.黑龙江中医药大学基础医学院
  • 收稿日期:2024-04-26 修回日期:2024-10-23 出版日期:2024-12-28 发布日期:2025-01-06
  • 通讯作者: 付强,E-mail:369060984@qq.com
  • 作者简介:陈星燕,女,(1999-),硕士研究生,从事与肿瘤相关的方剂配伍规律及药效物质基础的研究。
  • 基金资助:
    李冀全国名中医传承工作室建设项目

Research progress of RNA methylation in lung cancer

CHEN Xingyan1, LI Xue1, FU Qiang2   

  1. 1. Graduate School,Heilongjiang University of Chinese Medicine,Harbin 150040,China;
    2. School of Basic Medical Sciences,Heilongjiang University of Chinese Medicine
  • Received:2024-04-26 Revised:2024-10-23 Online:2024-12-28 Published:2025-01-06

摘要: 肺癌是常见的癌症之一,虽然对肺癌的风险、发展、免疫控制和治疗选择的理解有了较大的提高,但由于人们对肺癌致病机制认知有限,致其靶向治疗策略尚显不足。近年来,RNA甲基化是表观遗传学领域的研究热点,调控RNA甲基化的相关蛋白已成为癌症治疗的重要靶点。目前已有研究报道了RNA甲基化与肺癌中癌基因表达、糖酵解和免疫应答等生物过程之间的关系,但尚无深入的研究和分析。本文将从RNA甲基化与肺癌的关系入手,在现有研究的基础上探讨RNA甲基化与肺癌发病机制之间的关联,并讨论其未来发展方向。

关键词: 肺癌, m6A甲基化, 7-甲基鸟嘌呤, 5-甲基胞嘧啶, 1-甲基腺嘌呤

Abstract: Lung cancer is one of the most common cancers.Although there has been a significant improvement in our understanding the risk,development,immune control,and treatment options of lung cancer,the limited understanding of its pathogenesis has resulted in insufficient targeted treatment strategies.In recent years,RNA methylation has become a research hot topic in the field of epigenetics,and proteins regulating RNA methylation have become important targets for cancer treatment.At present,some studies have reported the relationship between RNA methylation and biological processes such as oncogene expression,glycolysis,and immune response in lung cancer,but there is still no in-depth research and analysis.This article will start with the relationship between RNA methylation and lung cancer,explore the association between RNA methylation and the pathogenesis of lung cancer based on existing research,and discuss its future development direction.

Key words: Lung cancer, M6A methylation, N7-methylguanosine, 5-methylcytosine, N1-methyladenosine

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