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COVID-19: Fighting the Invisible Enemy with MicroRNAs

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Date 2020 Aug 21
PMID 32814446
Citations 50
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Abstract

Introduction: The novel coronavirus (CoV) disease 2019 (COVID-19) is a viral infection that causes severe acute respiratory syndrome (SARS). It is believed that early reports of COVID-19 cases were noticed in December 2019 and soon after it became a global public health emergency. It is advised that COVID-19 transmits through human to human contact and in most cases, it remains asymptomatic. Several approaches are being utilized to control the outbreak of this fatal viral disease. microRNAs (miRNAs) are known signature therapeutic tool for the viral diseases; they are small non-coding RNAs that target the mRNAs to inhibit their post-transcriptional expression, therefore, impeding their functions, can serve as watchdogs or micromanagers in the cells.

Areas Covered: This review work delineated COVID-19 and its association with SARS and Middle East respiratory syndrome (MERS), the possible role of miRNAs in the pathogenesis of COVID-19, and therapeutic potential of miRNAs and their effective delivery to treat COVID-19.

Expert Opinion: This review highlighted the importance of various miRNAs and their potential role in fighting with this pandemic as therapeutic molecules utilizing nanotechnology.

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References
1.
Rebolledo-Mendez J, Vaishnav R, Cooper N, Friedland R . Cross-kingdom sequence similarities between human micro-RNAs and plant viruses. Commun Integr Biol. 2013; 6(5):e24951. PMC: 3821693. DOI: 10.4161/cib.24951. View

2.
Beuzelin D, Pitard B, Kaeffer B . Oral Delivery of miRNA With Lipidic Aminoglycoside Derivatives in the Breastfed Rat. Front Physiol. 2019; 10:1037. PMC: 6700720. DOI: 10.3389/fphys.2019.01037. View

3.
Rupaimoole R, Slack F . MicroRNA therapeutics: towards a new era for the management of cancer and other diseases. Nat Rev Drug Discov. 2017; 16(3):203-222. DOI: 10.1038/nrd.2016.246. View

4.
Krol J, Loedige I, Filipowicz W . The widespread regulation of microRNA biogenesis, function and decay. Nat Rev Genet. 2010; 11(9):597-610. DOI: 10.1038/nrg2843. View

5.
Bai Z, Wei J, Yu C, Han X, Qin X, Zhang C . Non-viral nanocarriers for intracellular delivery of microRNA therapeutics. J Mater Chem B. 2020; 7(8):1209-1225. DOI: 10.1039/c8tb02946f. View