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Published on: June 15, 2018
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.
Abstract:
Several types of cardiovascular cells use microRNA-21 ( miR-21 ), which has been linked to cardioprotection. In this study, we systematically reviewed the results of published papers on the therapeutic effect of miR-21 for myocardial infarction. Studies described the cardioprotective effects of miR-21 to reduce infarct size by improving angiogenesis, antiapoptotic, and anti-inflammatory mechanisms. Results suggest that cardioprotective effects of miR-21 may work synergistically to prevent the deterioration of cardiac function during postischemia. However, there are other results that indicate that miR-21 positively regulates tissue fibrosis, potentially worsening a postischemic injury. The dual functionalities of miR-21 occur through the targeting of genes and signaling pathways, such as PTEN , PDCD4 , KBTBD7 , NOS3 , STRN , and Spry-1 . This review provides insights into the future advancement of safe miR-21 -based genetic therapy in the treatment of myocardial infarction.
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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