Revisiting miRNA-21 as a Therapeutic Strategy for Myocardial Infarction: A Systematic Review

Vivisana Sothivelr1, Mohammad Y Hasan1, Shamin Mohd Saffian2

  • 1Centre for Drug and Herbal Development, Faculty of Pharmacy, Universiti Kebangsaan, Malaysia.

Insights

MicroRNA-21 (miR-21) shows dual effects in myocardial infarction, offering cardioprotection by reducing infarct size but also potentially worsening injury via fibrosis. Further research is needed for safe miR-21 therapy.

Area of Science:

  • Cardiovascular Biology
  • Molecular Medicine
  • Genetic Therapy

Background:

  • MicroRNA-21 (miR-21) is expressed in cardiovascular cells and implicated in cardioprotection.
  • Myocardial infarction (MI) is a leading cause of cardiac dysfunction.

Purpose of the Study:

  • To systematically review the therapeutic effects of miR-21 in myocardial infarction.
  • To elucidate the dual roles of miR-21 in post-ischemic cardiac injury.

Main Methods:

  • Systematic literature review of published studies on miR-21 and myocardial infarction.
  • Analysis of studies reporting miR-21's effects on infarct size, angiogenesis, apoptosis, inflammation, and fibrosis.

Main Results:

  • miR-21 demonstrates cardioprotective effects by enhancing angiogenesis, reducing apoptosis, and suppressing inflammation, thereby limiting infarct size.
  • miR-21 also promotes tissue fibrosis, potentially exacerbating post-ischemic injury.
  • These dual effects stem from miR-21's regulation of multiple genes and signaling pathways (e.g., PTEN, PDCD4).

Conclusions:

  • miR-21 exhibits complex, dual functionality in myocardial infarction.
  • Understanding these mechanisms is crucial for developing safe and effective miR-21-based genetic therapies for MI.
  • Further investigation is warranted to harness the protective aspects of miR-21 while mitigating its fibrotic effects.

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