Zhang Huan, Lu Wei, Tang Haoyue, Chen Aiqun, Gao Xiaofei, Zhu Congfei, Zhang Junjie
Department of Cardiology, Nanjing First Hospital, Nanjing Medical University, Nanjing 210006, China.
Department of Cardiology, Lianshui County People's Hospital, Affiliated Hospital of Kangda College, Nanjing Medical University, Huaian 223400, China.
Medicina (Kaunas). 2025 Jan 26;61(2):222. doi: 10.3390/medicina61020222.
N6-methyladenosine (m6A) is the most common and abundant internal co-transcriptional modification in eukaryotic RNAs. This modification is catalyzed by m6A methyltransferases, known as "writers", including and , and removed by demethylases, or "erasers", such as and . It is recognized by m6A-binding proteins, or "readers", such as , , , and . Cardiovascular diseases (CVDs) are the leading cause of morbidity and mortality worldwide. Recent studies indicate that m6A RNA modification plays a critical role in both the physiological and pathological processes involved in the initiation and progression of CVDs. In this review, we will explore how m6A RNA methylation impacts both the normal and disease states of the cardiovascular system. Our focus will be on recent advancements in understanding the biological functions, molecular mechanisms, and regulatory factors of m6A RNA methylation, along with its downstream target genes in various CVDs, such as atherosclerosis, ischemic diseases, metabolic disorders, and heart failure. We propose that the m6A RNA methylation pathway holds promise as a potential therapeutic target in cardiovascular disease.
Medicina (Kaunas). 2025-1-26
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