Key result
MicroRNAs regulate cardiac autophagy and mitophagy, driving pathogenesis across diverse heart diseases.
Why the study?
The role of microRNAs in regulating cardiac autophagy and their involvement in the pathogenesis of various cardiac disorders remains incompletely understood and controversial.
Answers are grounded in this paper and cite their sources.
May support miRNA-targeted autophagy modulation in heart disease; leaves open clinical validation in trials.
Autophagy, which is an evolutionarily conserved process according to the lysosomal degradation of cellular components, plays a critical role in maintaining cell homeostasis. Autophagy and mitochondria autophagy (mitophagy) contribute to the preservation of cardiac homeostasis in physiological settings. However, impaired or excessive autophagy is related to a variety of diseases. Recently, a close link between autophagy and cardiac disorders, including myocardial infarction, cardiac hypertrophy, cardiomyopathy, cardiac fibrosis, and heart failure, has been demonstrated. MicroRNAs (miRNAs) are a class of small non-coding RNAs with a length of approximately 21⁻22 nucleotides (nt), which are distributed widely in viruses, plants, protists, and animals. They function in mediating the post-transcriptional gene silencing. A growing number of studies have demonstrated that miRNAs regulate cardiac autophagy by suppressing the expression of autophagy-related genes in a targeted manner, which are involved in the pathogenesis of heart diseases. This review summarizes the role of microRNAs in cardiac autophagy and related cardiac disorders. Furthermore, we mainly focused on the autophagy regulation pathways, which consisted of miRNAs and their targeted genes.
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Sun et al. (2018) conducted a review in Cardiac diseases. MicroRNAs was evaluated. MicroRNAs regulate cardiac autophagy and mitophagy by modulating the expression of autophagy-related genes, playing a critical role in the pathogenesis of various heart diseases.
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