| Literature DB >> 33689451 |
Mehmet Altay Unal1, Ceylan Verda Bitirim1, Gokce Yagmur Summak1, Sidar Bereketoglu2, Inci Cevher Zeytin1, Omur Besbinar1, Cansu Gurcan1, Dunya Aydos1, Ezgi Goksoy1, Ebru Kocakaya1, Zeynep Eran1, Merve Murat3, Nil Demir3, Zeynep Busra Aksoy Ozer1, Julia Somers4, Emek Demir4, Hasan Nazir5, Sibel Aysil Ozkan6, Aykut Ozkul7, Alpay Azap8, Acelya Yilmazer1,9, Kamil Can Akcali1,10.
Abstract
Ribavirin is a guanosine analog with broad-spectrum antiviral activity against RNA viruses. Based on this, we aimed to show the anti-SARS-CoV-2 activity of this drug molecule via in vitro, in silico, and molecular techniques. Ribavirin showed antiviral activity in Vero E6 cells following SARS-CoV-2 infection, whereas the drug itself did not show any toxic effect over the concentration range tested. In silico analysis suggested that ribavirin has a broad-spectrum impact on SARS-CoV-2, acting at different viral proteins. According to the detailed molecular techniques, ribavirin was shown to decrease the expression of TMPRSS2 at both mRNA and protein levels 48 h after treatment. The suppressive effect of ribavirin in ACE2 protein expression was shown to be dependent on cell types. Finally, proteolytic activity assays showed that ribavirin also showed an inhibitory effect on the TMPRSS2 enzyme. Based on these results, we hypothesized that ribavirin may inhibit the expression of TMPRSS2 by modulating the formation of inhibitory G-quadruplex structures at the TMPRSS2 promoter. As a conclusion, ribavirin is a potential antiviral drug for the treatment against SARS-CoV-2, and it interferes with the effects of TMPRSS2 and ACE2 expression.Entities:
Keywords: COVID-19; drug; in silico; in vitro; médicament; pathway analysis; étude de voie de signalisation
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Year: 2021 PMID: 33689451 DOI: 10.1139/cjpp-2020-0734
Source DB: PubMed Journal: Can J Physiol Pharmacol ISSN: 0008-4212 Impact factor: 2.273