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Updated: Apr 19, 2026

Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
MicroRNAs in myocardial infarction
Reinier A Boon1, Stefanie Dimmeler1
1Institute for Cardiovascular Regeneration, Center of Molecular Medicine, Goethe University, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.
Abstract:
MicroRNAs (miRNAs) are small noncoding RNAs that block translation or induce degradation of mRNA and thereby control patterns of gene expression. Acute myocardial infarction is a common cardiovascular event that results in cardiac remodelling and can consequently lead to the development of chronic heart failure. Several miRNAs have been shown to control important processes that contribute to the pathophysiological consequences of acute myocardial infarction. miRNAs can either promote or inhibit cardiomyocyte cell death, and also regulate postischaemic neovascularization. Cardiac regeneration can also be regulated by miRNAs that control cardiomyocyte proliferation or interfere with cardioprotective effects mediated by stem or progenitor cells. miRNAs can also be used for direct reprogramming of cardiac fibroblasts into cardiomyocytes. In this Review, we focus on the current understanding of the role of miRNAs in these processes, and particularly discuss the therapeutic potential of miRNAs in treating acute myocardial infarction.
Insights
MicroRNAs (miRNAs) regulate gene expression and are crucial in heart attack recovery. This review explores their therapeutic potential for treating acute myocardial infarction and improving heart function.
Area of Science:
- Molecular Biology
- Cardiovascular Research
- Biochemistry
Background:
- MicroRNAs (miRNAs) are small noncoding RNAs regulating gene expression by inhibiting mRNA translation or promoting degradation.
- Acute myocardial infarction (AMI) triggers cardiac remodeling, potentially leading to chronic heart failure.
- Specific miRNAs influence key processes in AMI pathophysiology, including cell death and neovascularization.
Purpose of the Study:
- To review the current understanding of microRNA roles in the pathophysiological consequences of acute myocardial infarction.
- To highlight the therapeutic potential of microRNAs for treating acute myocardial infarction.
Main Methods:
- Literature review of studies investigating microRNA function in cardiac remodeling, cell death, neovascularization, and regeneration post-AMI.
- Analysis of research on microRNA-mediated direct reprogramming of cardiac fibroblasts.
- Synthesis of findings on the therapeutic applications of miRNAs in the context of acute myocardial infarction.
Main Results:
- MicroRNAs modulate cardiomyocyte cell death and post-ischemic neovascularization.
- MicroRNAs regulate cardiac regeneration by controlling cardiomyocyte proliferation and stem/progenitor cell interactions.
- MicroRNAs show promise for direct reprogramming of cardiac fibroblasts into cardiomyocytes.
Conclusions:
- MicroRNAs play multifaceted roles in the response to acute myocardial infarction, influencing cell death, regeneration, and repair.
- Targeting microRNAs offers significant therapeutic potential for managing acute myocardial infarction and preventing heart failure progression.
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