Qin Lifei, Zeng Xinya, Qiu Xinze, Chen Xingmei, Liu Shiquan
Department of Gastroenterology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Front Oncol. 2024 Dec 3;14:1467850. doi: 10.3389/fonc.2024.1467850. eCollection 2024.
Tumor angiogenesis is a characteristics of malignant cancer progression that facilitates cancer cell growth, diffusion and metastasis, and has an indispensable role in cancer development. N6-methyladenosine (m6A) is among the most prevalent internal modifications in eukaryotic RNAs, and has considerable influence on RNA metabolism, including its transcription, splicing, localization, translation, recognition, and degradation. The m6A modification is generated by m6A methyltransferases ("writers"), removed by m6A demethylases ("erasers"), and recognized by m6A-binding proteins ("readers"). There is accumulating evidence that abnormal m6A modification is involved in the pathogenesis of multiple diseases, including cancers, and promotes cancer occurrence, development, and progression through its considerable impact on oncoprotein expression. Furthermore, increasing studies have demonstrated that m6A modification can influence angiogenesis in cancers through multiple pathways to regulate malignant processes. In this review, we elaborate the role of m6A modification in tumor angiogenesis-related molecules and pathways in detail, providing insights into the interactions between m6A and tumor angiogenesis. Moreover, we describe how targeting m6A modification in combination with anti-angiogenesis drugs is expected to be a promising anti-tumor treatment strategy, with potential value for addressing the challenge of drug resistance.
肿瘤血管生成是恶性肿瘤进展的一个特征,它促进癌细胞的生长、扩散和转移,在癌症发展中起着不可或缺的作用。N6-甲基腺苷(m6A)是真核RNA中最普遍的内部修饰之一,对RNA代谢有相当大的影响,包括其转录、剪接、定位、翻译、识别和降解。m6A修饰由m6A甲基转移酶(“书写器”)产生,由m6A去甲基化酶(“擦除器”)去除,并由m6A结合蛋白(“读取器”)识别。越来越多的证据表明,异常的m6A修饰参与包括癌症在内的多种疾病的发病机制,并通过其对癌蛋白表达的重大影响促进癌症的发生、发展和进展。此外,越来越多的研究表明,m6A修饰可通过多种途径影响癌症中的血管生成,从而调节恶性过程。在这篇综述中,我们详细阐述了m6A修饰在肿瘤血管生成相关分子和途径中的作用,深入了解m6A与肿瘤血管生成之间的相互作用。此外,我们描述了靶向m6A修饰并联合抗血管生成药物有望成为一种有前景的抗肿瘤治疗策略,对于应对耐药性挑战具有潜在价值。