Liu Xiaocui, Kan Xuefeng
Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hubei Provincial Clinical Research Center for Precision Radiology and Interventional Medicine, Wuhan, China.
Front Oncol. 2025 Aug 1;15:1629864. doi: 10.3389/fonc.2025.1629864. eCollection 2025.
N6-methyladenosine (m6A) is a reversible mRNA modification that plays important roles in malignant tumor processes. m6A modification has emerged as a significant research focus. Studies on the functions and mechanisms of m6A and its regulatory factors across various tumors have grown increasingly comprehensive and in-depth. Accumulating evidence has demonstrated that m6A modifications and their associated regulatory proteins can serve as biomarkers for cancer treatment and prognosis. Consequently, there has been a surge in research on the development and application of m6A regulatory factor inhibitors, particularly regarding their efficacy and mechanisms in tumor therapy. These advancements not only enhance the understanding of their therapeutic potential in diverse cancers but also facilitate their integration with existing treatments, accelerating the design of more effective, specific, and selective inhibitors. Such efforts hold promise for advancing m6A-targeted pharmaceutical development and promoting clinical applications. This review summarizes small-molecule and peptide inhibitors of m6A regulators for malignant tumors.
N6-甲基腺苷(m6A)是一种可逆的mRNA修饰,在恶性肿瘤进程中发挥重要作用。m6A修饰已成为一个重要的研究焦点。关于m6A及其调控因子在各种肿瘤中的功能和机制的研究越来越全面和深入。越来越多的证据表明,m6A修饰及其相关调控蛋白可作为癌症治疗和预后的生物标志物。因此,关于m6A调控因子抑制剂的开发和应用的研究激增,特别是关于它们在肿瘤治疗中的疗效和机制。这些进展不仅加深了我们对其在多种癌症中的治疗潜力的理解,还促进了它们与现有治疗方法的整合,加速了更有效、特异和选择性抑制剂的设计。这些努力有望推动以m6A为靶点的药物开发并促进临床应用。本综述总结了用于恶性肿瘤的m6A调节剂的小分子和肽类抑制剂。