Li Longbo, Xu Nannan, Liu Jia, Chen Zhenzhen, Liu Xu, Wang Junnan
Department of Cardiology, Second Hospital of Jilin University, Changchun, China.
Front Genet. 2022 Jun 28;13:908976. doi: 10.3389/fgene.2022.908976. eCollection 2022.
Cardiovascular disease (CVD) is a leading cause of morbidity and mortality worldwide. Recent studies have shown that n6-methyladenosine (m6A) plays a major role in cardiovascular homeostasis and pathophysiology. These studies have confirmed that m6A methylation affects the pathophysiology of cardiovascular diseases by regulating cellular processes such as differentiation, proliferation, inflammation, autophagy, and apoptosis. Moreover, plenty of research has confirmed that m6A modification can delay the progression of CVD via the post-transcriptional regulation of RNA. However, there are few available summaries of m6A modification regarding CVD. In this review, we highlight advances in CVD-specific research concerning m6A modification, summarize the mechanisms underlying the involvement of m6A modification during the development of CVD, and discuss the potential of m6A modification as a therapeutic target of CVD.
心血管疾病(CVD)是全球发病和死亡的主要原因。最近的研究表明,N6-甲基腺苷(m6A)在心血管稳态和病理生理学中起主要作用。这些研究证实,m6A甲基化通过调节细胞分化、增殖、炎症、自噬和凋亡等过程影响心血管疾病的病理生理学。此外,大量研究证实,m6A修饰可通过RNA的转录后调控延缓CVD的进展。然而,关于CVD的m6A修饰的可用总结很少。在这篇综述中,我们重点介绍了关于m6A修饰的CVD特异性研究进展,总结了m6A修饰在CVD发生发展过程中的作用机制,并讨论了m6A修饰作为CVD治疗靶点的潜力。