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dc.contributor.authorMarkovic, Jovana
dc.contributor.authorSharma, Amar Deep
dc.contributor.authorBalakrishnan, Asha
dc.date.accessioned2020-11-19T13:56:14Z
dc.date.available2020-11-19T13:56:14Z
dc.date.issued2020-07-23
dc.identifier.citationCells. 2020 Jul 23;9(8):1767. doi: 10.3390/cells9081767.en_US
dc.identifier.pmid32717951
dc.identifier.doi10.3390/cells9081767
dc.identifier.urihttp://hdl.handle.net/10033/622598
dc.description.abstractThe last decade has witnessed significant advancements in our understanding of how small noncoding RNAs, such as microRNAs (miRNAs), regulate disease progression. One such miRNA, miR-221, has been shown to play a key role in the progression of liver fibrosis, a common feature of most liver diseases. Many reports have demonstrated the upregulation of miR-221 in liver fibrosis caused by multiple etiologies such as viral infections and nonalcoholic steatohepatitis. Inhibition of miR-221 via different strategies has shown promising results in terms of the suppression of fibrogenic gene signatures in vitro, as well as in vivo, in independent mouse models of liver fibrosis. In addition, miR-221 has also been suggested as a noninvasive serum biomarker for liver fibrosis and cirrhosis. In this review, we discuss the biology of miR-221, its significance and use as a biomarker during progression of liver fibrosis, and finally, potential and robust approaches that can be utilized to suppress liver fibrosis via inhibition of miR-221.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectHCCen_US
dc.subjectNASHen_US
dc.subjectliver fibrosisen_US
dc.subjectmiR-221en_US
dc.subjectnoninvasive biomarkeren_US
dc.titleMicroRNA-221: A Fine Tuner and Potential Biomarker of Chronic Liver Injury.en_US
dc.typeReviewen_US
dc.identifier.eissn2073-4409
dc.contributor.departmentHZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany.en_US
dc.identifier.journalCellsen_US
dc.source.volume9
dc.source.issue8
refterms.dateFOA2020-11-19T13:56:15Z
dc.source.journaltitleCells
dc.source.countrySwitzerland


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Attribution-NonCommercial-ShareAlike 4.0 International
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-ShareAlike 4.0 International