Cargando…

Circulating exosomal long non‐coding RNAs in patients with acute myocardial infarction

Exosomes are attracting considerable interest in the cardiovascular field as the wide range of their functions is recognized in acute myocardial infarction (AMI). However, the regulatory role of exosomal long non‐coding RNAs (lncRNAs) in AMI remains largely unclear. Exosomes were isolated from the p...

Descripción completa

Detalles Bibliográficos
Autores principales: Zheng, Mei‐Li, Liu, Xiao‐Yan, Han, Rui‐Juan, Yuan, Wen, Sun, Kai, Zhong, Jiu‐Chang, Yang, Xin‐Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417690/
https://www.ncbi.nlm.nih.gov/pubmed/32649009
http://dx.doi.org/10.1111/jcmm.15589
_version_ 1783569549639024640
author Zheng, Mei‐Li
Liu, Xiao‐Yan
Han, Rui‐Juan
Yuan, Wen
Sun, Kai
Zhong, Jiu‐Chang
Yang, Xin‐Chun
author_facet Zheng, Mei‐Li
Liu, Xiao‐Yan
Han, Rui‐Juan
Yuan, Wen
Sun, Kai
Zhong, Jiu‐Chang
Yang, Xin‐Chun
author_sort Zheng, Mei‐Li
collection PubMed
description Exosomes are attracting considerable interest in the cardiovascular field as the wide range of their functions is recognized in acute myocardial infarction (AMI). However, the regulatory role of exosomal long non‐coding RNAs (lncRNAs) in AMI remains largely unclear. Exosomes were isolated from the plasma of AMI patients and controls, and the sequencing profiles and twice qRT‐PCR validations of exosomal lncRNAs were performed. A total of 518 differentially expressed lncRNAs were detected over two‐fold change, and 6 kinds of lncRNAs were strikingly elevated in AMI patients with top fold change and were selected to perform subsequent validation. In the two validations, lncRNAs ENST00000556899.1 and ENST00000575985.1 were significantly up‐regulated in AMI patients compared with controls. ROC curve analysis revealed that circulating exosomal lncRNAs ENST00000556899.1 and ENST00000575985.1 yielded the area under the curve values of 0.661 and 0.751 for AMI, respectively. Moreover, ENST00000575985.1 showed more significant relationship with clinical parameters, including inflammatory biomarkers, prognostic indicators and myocardial damage markers. Multivariate logistic model exhibited positive association of ENST00000575985.1 with the risk of heart failure in AMI patients. In summary, our data demonstrated that circulating exosomal lncRNAs ENST00000556899.1 and ENST00000575985.1 are elevated in patients with AMI, functioning as potential biomarkers for predicting the prognosis of pateints with AMI.
format Online
Article
Text
id pubmed-7417690
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-74176902020-08-11 Circulating exosomal long non‐coding RNAs in patients with acute myocardial infarction Zheng, Mei‐Li Liu, Xiao‐Yan Han, Rui‐Juan Yuan, Wen Sun, Kai Zhong, Jiu‐Chang Yang, Xin‐Chun J Cell Mol Med Original Articles Exosomes are attracting considerable interest in the cardiovascular field as the wide range of their functions is recognized in acute myocardial infarction (AMI). However, the regulatory role of exosomal long non‐coding RNAs (lncRNAs) in AMI remains largely unclear. Exosomes were isolated from the plasma of AMI patients and controls, and the sequencing profiles and twice qRT‐PCR validations of exosomal lncRNAs were performed. A total of 518 differentially expressed lncRNAs were detected over two‐fold change, and 6 kinds of lncRNAs were strikingly elevated in AMI patients with top fold change and were selected to perform subsequent validation. In the two validations, lncRNAs ENST00000556899.1 and ENST00000575985.1 were significantly up‐regulated in AMI patients compared with controls. ROC curve analysis revealed that circulating exosomal lncRNAs ENST00000556899.1 and ENST00000575985.1 yielded the area under the curve values of 0.661 and 0.751 for AMI, respectively. Moreover, ENST00000575985.1 showed more significant relationship with clinical parameters, including inflammatory biomarkers, prognostic indicators and myocardial damage markers. Multivariate logistic model exhibited positive association of ENST00000575985.1 with the risk of heart failure in AMI patients. In summary, our data demonstrated that circulating exosomal lncRNAs ENST00000556899.1 and ENST00000575985.1 are elevated in patients with AMI, functioning as potential biomarkers for predicting the prognosis of pateints with AMI. John Wiley and Sons Inc. 2020-07-10 2020-08 /pmc/articles/PMC7417690/ /pubmed/32649009 http://dx.doi.org/10.1111/jcmm.15589 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Zheng, Mei‐Li
Liu, Xiao‐Yan
Han, Rui‐Juan
Yuan, Wen
Sun, Kai
Zhong, Jiu‐Chang
Yang, Xin‐Chun
Circulating exosomal long non‐coding RNAs in patients with acute myocardial infarction
title Circulating exosomal long non‐coding RNAs in patients with acute myocardial infarction
title_full Circulating exosomal long non‐coding RNAs in patients with acute myocardial infarction
title_fullStr Circulating exosomal long non‐coding RNAs in patients with acute myocardial infarction
title_full_unstemmed Circulating exosomal long non‐coding RNAs in patients with acute myocardial infarction
title_short Circulating exosomal long non‐coding RNAs in patients with acute myocardial infarction
title_sort circulating exosomal long non‐coding rnas in patients with acute myocardial infarction
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417690/
https://www.ncbi.nlm.nih.gov/pubmed/32649009
http://dx.doi.org/10.1111/jcmm.15589
work_keys_str_mv AT zhengmeili circulatingexosomallongnoncodingrnasinpatientswithacutemyocardialinfarction
AT liuxiaoyan circulatingexosomallongnoncodingrnasinpatientswithacutemyocardialinfarction
AT hanruijuan circulatingexosomallongnoncodingrnasinpatientswithacutemyocardialinfarction
AT yuanwen circulatingexosomallongnoncodingrnasinpatientswithacutemyocardialinfarction
AT sunkai circulatingexosomallongnoncodingrnasinpatientswithacutemyocardialinfarction
AT zhongjiuchang circulatingexosomallongnoncodingrnasinpatientswithacutemyocardialinfarction
AT yangxinchun circulatingexosomallongnoncodingrnasinpatientswithacutemyocardialinfarction