Back to Search Start Over

The role of microRNAs in solving COVID-19 puzzle from infection to therapeutics: A mini-review

Authors :
Paula Roxana Reyes-Pérez
Surajit Pathak
Aashish Srivastava
Samik Chakraborty
Sujay Paul
Carolina Estrada-Meza
Anindya Bandyopadhyay
Antara Banerjee
Luis Alberto Bravo Vázquez
Rafael Arturo Aponte Alburquerque
Source :
Virus Research
Publication Year :
2021

Abstract

Nowadays, one of the major global health concerns is coronavirus disease 2019 (COVID-19), which is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Even though numerous treatments and vaccines to combat this virus are currently under development, the detailed molecular mechanisms underlying the pathogenesis of this disease are yet to be elucidated to design future therapeutic tools against SARS-CoV-2 variants. MicroRNAs (miRNAs) are small (20-24 nucleotides), non-coding RNA molecules that regulate post-transcriptional gene expression. Recently, it has been demonstrated that both host and viral-encoded miRNAs are crucial for the successful infection of SARS-CoV-2. For instance, dysregulation of miRNAs that modulate multiple genes expressed in COVID-19 patients with comorbidities (e.g., type 2 diabetes, lung adenocarcinoma, and cerebrovascular disorders) could affect the severity of the disease. Thus, altered expression levels of circulating miRNAs might be helpful to diagnose this illness and forecast whether a COVID-19 patient could develop a severe state of the disease. Besides, researchers have found a number of miRNAs could inhibit the expression of proteins, such as ACE2, TMPRSS2, spike, and Nsp12, involved in the life cycle of SARS-CoV-2. Accordingly, miRNAs represent potential biomarkers and therapeutic targets for this devastating viral disease. Therefore, in this current review, we present the recent discoveries regarding the clinical relevance and biological roles of miRNAs in COVID-19.

Details

ISSN :
18727492
Volume :
308
Database :
OpenAIRE
Journal :
Virus research
Accession number :
edsair.doi.dedup.....6a7085e6d081bafa25567f0fddb90fb9