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The Current State of MicroRNAs as Restenosis Biomarkers

In-stent restenosis corresponds to the diameter reduction of coronary vessels following percutaneous coronary intervention (PCI), an invasive procedure in which a stent is deployed into the coronary arteries, producing profuse neointimal hyperplasia. The reasons for this process to occur still lack...

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Autores principales: Varela, Nelson, Lanas, Fernando, Salazar, Luis A., Zambrano, Tomás
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967329/
https://www.ncbi.nlm.nih.gov/pubmed/31998354
http://dx.doi.org/10.3389/fgene.2019.01247
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author Varela, Nelson
Lanas, Fernando
Salazar, Luis A.
Zambrano, Tomás
author_facet Varela, Nelson
Lanas, Fernando
Salazar, Luis A.
Zambrano, Tomás
author_sort Varela, Nelson
collection PubMed
description In-stent restenosis corresponds to the diameter reduction of coronary vessels following percutaneous coronary intervention (PCI), an invasive procedure in which a stent is deployed into the coronary arteries, producing profuse neointimal hyperplasia. The reasons for this process to occur still lack a clear answer, which is partly why it remains as a clinically significant problem. As a consequence, there is a vigorous need to identify useful non-invasive biomarkers to differentiate and follow-up subjects at risk of developing restenosis, and due to their extraordinary stability in several bodily fluids, microRNA research has received extensive attention to accomplish this task. This review depicts the current understanding, diagnostic potential and clinical challenges of microRNA molecules as possible blood-based restenosis biomarkers.
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spelling pubmed-69673292020-01-29 The Current State of MicroRNAs as Restenosis Biomarkers Varela, Nelson Lanas, Fernando Salazar, Luis A. Zambrano, Tomás Front Genet Genetics In-stent restenosis corresponds to the diameter reduction of coronary vessels following percutaneous coronary intervention (PCI), an invasive procedure in which a stent is deployed into the coronary arteries, producing profuse neointimal hyperplasia. The reasons for this process to occur still lack a clear answer, which is partly why it remains as a clinically significant problem. As a consequence, there is a vigorous need to identify useful non-invasive biomarkers to differentiate and follow-up subjects at risk of developing restenosis, and due to their extraordinary stability in several bodily fluids, microRNA research has received extensive attention to accomplish this task. This review depicts the current understanding, diagnostic potential and clinical challenges of microRNA molecules as possible blood-based restenosis biomarkers. Frontiers Media S.A. 2020-01-10 /pmc/articles/PMC6967329/ /pubmed/31998354 http://dx.doi.org/10.3389/fgene.2019.01247 Text en Copyright © 2020 Varela, Lanas, Salazar and Zambrano http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Varela, Nelson
Lanas, Fernando
Salazar, Luis A.
Zambrano, Tomás
The Current State of MicroRNAs as Restenosis Biomarkers
title The Current State of MicroRNAs as Restenosis Biomarkers
title_full The Current State of MicroRNAs as Restenosis Biomarkers
title_fullStr The Current State of MicroRNAs as Restenosis Biomarkers
title_full_unstemmed The Current State of MicroRNAs as Restenosis Biomarkers
title_short The Current State of MicroRNAs as Restenosis Biomarkers
title_sort current state of micrornas as restenosis biomarkers
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967329/
https://www.ncbi.nlm.nih.gov/pubmed/31998354
http://dx.doi.org/10.3389/fgene.2019.01247
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