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                  <mods:namePart>Palomer, Xavier</mods:namePart>
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                  <mods:namePart>Capdevila-Busquets, E.</mods:namePart>
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                  <mods:namePart>Botteri, G.</mods:namePart>
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                  <mods:namePart>Davidson, Mercy M.</mods:namePart>
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                  <mods:namePart>Rodríguez, Cristina</mods:namePart>
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                  <mods:namePart>Martínez-González, José</mods:namePart>
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                  <mods:namePart>Vidal, Francisco</mods:namePart>
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                  <mods:namePart>Barroso, Emma</mods:namePart>
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                  <mods:namePart>Chan, Tung O.</mods:namePart>
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                  <mods:namePart>Feldman, Arthur M.</mods:namePart>
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                  <mods:namePart>Vázquez-Carrera, Manuel</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Universitat Autònoma de Barcelona</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-11-04T08:22:14Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2015</mods:dateIssued>
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               <mods:identifier type="none"/>
               <mods:identifier type="uri">http://hdl.handle.net/2072/477136</mods:identifier>
               <mods:abstract>miR-146a is a microRNA whose transcript levels are induced in the heart upon activation of NF-κB, a transcription factor induced by proinflammatory molecules (such as TNF-α) that is strongly related to the pathogenesis of cardiac disorders. The main goal of this study consisted of studying new roles of miR-146a in cardiac pathological processes caused by the pro-inflammatory cytokine TNF-α.Our results demonstrate that miR-146a transcript levels were sharply increased in cardiac ventricular tissue of transgenic mice with specific overexpression of TNF-α in the heart, and also in a cardiomyocyte cell line of human origin (AC16) exposed to TNF-α. Among all the in silico predicted miR-146a target genes, Fos mRNA and protein levels notably decreased after TNF-α treatment or miR-146a overexpression. These changes correlated with a diminution in the DNA-binding activity of AP-1, the Fos-containing transcription factor complex. Interestingly, AP-1 inhibitionwas accompanied by a reduction in matrix metalloproteinase (MMP)-9 mRNA levels in human cardiac cells. The specific regulation of this MMP by miR-146a was further confirmed at the secretion and enzymatic activity levels, aswell as after anti-miR-mediated miR-146a inhibition. The results reported here demonstrate that Fos is a direct target of miR-146a activity and that downregulation of the Fos-AP-1 pathway bymiR-146a has the capacity to inhibit MMP-9 activity. Given that MMP-9 is an AP-1 target gene involvedin cardiac remodeling,myocardial dysfunction and progression of heart failure, these findings suggest that miR-146a might be a new and promising therapeutic tool for treating cardiac disorders associated with enhanced inflammation in the heart.</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">open access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. https://creativecommons.org/licenses/by/4.0/</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Cardiac remodeling</mods:topic>
               </mods:subject>
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                  <mods:topic>Fos</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Inflammation</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Matrix metalloproteinase-9</mods:topic>
               </mods:subject>
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                  <mods:topic>Mir-146a</mods:topic>
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                  <mods:title>MiR-146a targets Fos expression in human cardiac cells</mods:title>
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