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m6A Methylation in Cardiovascular Diseases: From Mechanisms to Therapeutic Potential
Longbo Li1, Nannan Xu1, Jia Liu1
1Department of Cardiology, Second Hospital of Jilin University, Changchun, China.
Insights
n6-methyladenosine (m6A) modification is crucial in cardiovascular disease (CVD) pathophysiology. This RNA modification regulates key cellular processes and may offer new therapeutic targets for delaying CVD progression.
Area of Science:
- Biochemistry
- Molecular Biology
- Cardiology
Background:
- Cardiovascular disease (CVD) is a major global health burden.
- n6-methyladenosine (m6A) modification is increasingly recognized for its role in cardiovascular health and disease.
- m6A influences critical cellular processes involved in CVD pathogenesis.
Purpose of the Study:
- To review recent advances in m6A modification research related to CVD.
- To summarize the mechanisms by which m6A affects CVD development.
- To explore the therapeutic potential of targeting m6A modification for CVD.
Main Methods:
- Literature review of studies on m6A modification in cardiovascular disease.
- Analysis of m6A's role in regulating cellular processes like differentiation, proliferation, inflammation, autophagy, and apoptosis.
- Examination of m6A's post-transcriptional regulatory functions in RNA.
Main Results:
- m6A methylation significantly impacts cardiovascular homeostasis and pathophysiology.
- m6A modification regulates key cellular pathways implicated in CVD.
- Evidence suggests m6A can delay CVD progression through RNA regulation.
Conclusions:
- m6A modification is a critical regulator in the context of cardiovascular disease.
- Understanding m6A mechanisms provides insights into CVD development.
- Targeting m6A represents a promising therapeutic strategy for cardiovascular diseases.
Abstract:
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.
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