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Role of microRNAs in COVID-19 with implications for therapeutics
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. University of Sussex, United Kingdom.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. University of Sussex, United Kingdom.
Number of Authors: 32021 (English)In: Biomedicine and Pharmacotherapy, ISSN 0753-3322, E-ISSN 1950-6007, Vol. 144, article id 112247Article in journal (Refereed) Published
Abstract [en]

COVID-19 is a pneumonia-like disease with highly transmittable and pathogenic properties caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which infects both animals and humans. Although many efforts are currently underway to test possible therapies, there is no specific FDA approved drug against SARS-CoV-2 yet. miRNA-directed gene regulation controls the majority of biological processes. In addition, the development and progression of several human diseases are associated with dysregulation of miRNAs. In this regard, it has been shown that changes in miRNAs are linked to severity of COVID-19 especially in patients with respiratory diseases, diabetes, heart failure or kidney problems. Therefore, targeting these small noncoding-RNAs could potentially alleviate complications from COVID-19. Here, we will review the roles and importance of host and RNA virus encoded miRNAs in COVID-19 pathogenicity and immune response. Then, we focus on potential miRNA therapeutics in the patients who are at increased risk for severe disease.

Place, publisher, year, edition, pages
2021. Vol. 144, article id 112247
Keywords [en]
SARS-CoV-2, Coronavirus, miRNAs, Anti-miRNA therapy, miRNA therapy
National Category
Infectious Medicine
Identifiers
URN: urn:nbn:se:su:diva-198626DOI: 10.1016/j.biopha.2021.112247ISI: 000704917500001PubMedID: 34601190OAI: oai:DiVA.org:su-198626DiVA, id: diva2:1611389
Available from: 2021-11-15 Created: 2021-11-15 Last updated: 2023-03-20Bibliographically approved

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Arghiani, NahidNissan, Tracy

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