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MicroRNAs-The Heart of Post-Myocardial Infarction Remodeling. | LitMetric

AI Article Synopsis

  • - Myocardial infarction (MI) often leads to serious complications like heart failure due to healing responses that cause changes in the heart known as left ventricular remodeling (LVR).
  • - Transforming growth factor-beta (TGF-β) signaling pathways activate cardiac fibroblasts and lead to excessive collagen production, influencing the healing process after MI, with microRNAs (miRNAs) playing a significant role in this modulation.
  • - The review highlights over 30 miRNAs involved in post-MI LVR, compares their contradictory functions, and discusses their potential as biomarkers for heart failure, along with relevant human trial evidence.

Article Abstract

Myocardial infarction (MI) is one of the most frequent cardiac emergencies, with significant potential for mortality. One of the major challenges of the post-MI healing response is that replacement fibrosis could lead to left ventricular remodeling (LVR) and heart failure (HF). This process involves canonical and non-canonical transforming growth factor-beta (TGF-β) signaling pathways translating into an intricate activation of cardiac fibroblasts and disproportionate collagen synthesis. Accumulating evidence has indicated that microRNAs (miRNAs) significantly contribute to the modulation of these signaling pathways. This review summarizes the recent updates regarding the molecular mechanisms underlying the role of the over 30 miRNAs involved in post-MI LVR. In addition, we compare the contradictory roles of several multifunctional miRNAs and highlight their potential use in pressure overload and ischemia-induced fibrosis. Finally, we discuss their attractive role as prognostic biomarkers for HF, highlighting the most relevant human trials involving these miRNAs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469128PMC
http://dx.doi.org/10.3390/diagnostics11091675DOI Listing

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