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Updated: Jan 9, 2026

Exploring the Arginine Methylome by Nuclear Magnetic Resonance Spectroscopy
Published on: December 16, 2021
The PRMT-mediated arginine methylation: From molecular mechanisms to therapeutic targets in cardiovascular diseases
Jia-Qi Tang1, Yang-Kai Wang2, Qi Shen2
1College of Basic Medical Sciences, Naval Medical University (Second Military Medical University), Shanghai, 200433, China; Naval Medical Center, Naval Medical University (Second Military Medical University), Shanghai, 200433, China.
Insights
Protein arginine methyltransferases (PRMTs) are implicated in cardiovascular diseases (CVDs). This review explores their mechanisms and therapeutic potential for conditions like atherosclerosis and heart failure.
Area of Science:
- Biochemistry and Molecular Biology
- Cardiology
- Translational Medicine
Background:
- Cardiovascular diseases (CVDs) are a leading global cause of death, with complex pathogenesis hindering effective treatments.
- Current therapeutic strategies for many CVDs are limited, necessitating novel approaches for early detection and intervention.
Purpose of the Study:
- To review the mechanistic roles of protein arginine methyltransferases (PRMTs) in the pathogenesis of various cardiovascular diseases.
- To explore the therapeutic and diagnostic potential of PRMTs in clinical practice for CVD management.
Main Methods:
- Comprehensive literature review of studies investigating PRMTs in cardiovascular contexts.
- Analysis of evidence linking PRMTs to molecular mechanisms in atherosclerosis, hypertension, heart failure, ischemic heart disease, and arrhythmogenic cardiomyopathy.
Main Results:
- Altered levels of PRMTs are observed in patients with CVDs.
- PRMTs modulate key signaling molecules, including asymmetric dimethylarginine and nitric oxide synthase, impacting disease progression.
- PRMTs play multifaceted roles in major cardiovascular conditions.
Conclusions:
- PRMTs are mechanistically involved in the pathogenesis of diverse cardiovascular diseases.
- Understanding PRMTs' functions provides a foundation for developing novel diagnostic and therapeutic strategies for CVDs.
Abstract:
Cardiovascular diseases (CVDs) are the preeminent cause of mortality among non-communicable diseases globally, posing a significant threat to human health and placing a considerable socioeconomic burden on patients and healthcare systems. Given pathogenesis complexity, many cardiovascular conditions lack effective early detection or disease-halting therapies. This review integrates emerging protein arginine methyltransferases (PRMTs) evidence to identify their mechanistic roles and therapeutic potential in CVDs. Accumulating evidence indicates that levels of PRMTs are altered in patients with CVDs, and they are directly implicated in disease pathogenesis by modulating levels and activities of other downstream signaling molecules and enzymes in the body, such as asymmetric dimethylarginine and nitric oxide synthase. Hence, this review summarizes the mechanisms of PRMTs' effects and the regulatory factors influencing its activity, especially the roles of PRMTs in atherosclerosis, hypertension, heart failure, ischemic heart disease, and arrhythmogenic cardiomyopathy. By elucidating the multifaceted involvement of PRMTs in these conditions, this review aims to establish a theoretical foundation for exploring the potential diagnostic and therapeutic value of PRMTs in clinical practice.
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