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MicroRNA 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury

BACKGROUND: Ischemia/reperfusion (I/R) injury of heart is one of the major causes of acute cardiac injury, which may result in worsening or even loss of heart function. With novel microRNAs being evolutionarily discovered, numbers of them remained functionally unknown. We aimed to discover novel mic...

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Autores principales: Chen, Yuanyuan, Ye, Xing, Yan, Fengping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824141/
https://www.ncbi.nlm.nih.gov/pubmed/31672150
http://dx.doi.org/10.1186/s13000-019-0894-1
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author Chen, Yuanyuan
Ye, Xing
Yan, Fengping
author_facet Chen, Yuanyuan
Ye, Xing
Yan, Fengping
author_sort Chen, Yuanyuan
collection PubMed
description BACKGROUND: Ischemia/reperfusion (I/R) injury of heart is one of the major causes of acute cardiac injury, which may result in worsening or even loss of heart function. With novel microRNAs being evolutionarily discovered, numbers of them remained functionally unknown. We aimed to discover novel microRNAs with therapeutic or diagnostic potential in the setting of early cardiac I/R injury. METHODS: Cardiac electrical activity, biochemical detection and histopathology analysis were performed to reveal early changes of cardiac I/R injury. A microRNA array was performed to screen differential microRNAs in the mouse model of cardiac I/R injury. The differentially expressed microRNAs were validated in cardiac tissues and in serum samples. RESULTS: The abnormality in electrocardiogram and increases in serum cTnI levels suggested the successful establishment of cardiac I/R injury in mice. A total of 1882 microRNAs were identified, of which 11 were significantly down-regulated and 41 were significantly up-regulated at 3 h post reperfusion. microRNA 223-3p and microRNA 3113-5p were among the mostly altered microRNAs and were validated to be up-regulated within the early hours of I/R injury in heart tissues. In the circulating system, cTnI, a sensitive marker of cardiac injury, or microRNA 223-3p only increased within the first 6 h post I/R injury. However, microRNA 3113-5p stably increased in the serum, keeping an increase of 2.5-fold throughout the 24 h. In the human serum samples, microRNA 3113-5p was detected to be significantly upregulated as soon as 3 h after I/R stimuli and kept significantly higher levels within the 48 h. CONCLUSION: This is the first study that reported the functional roles of microRNA 3113-5p in cardiovascular system. Our data suggested that cardiac microRNA 3113-5p might be a useful target for therapeutic purposes and circulating microRNA 3113-5p might serve as a stable marker for early diagnosis of cardiac I/R injury.
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spelling pubmed-68241412019-11-06 MicroRNA 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury Chen, Yuanyuan Ye, Xing Yan, Fengping Diagn Pathol Research BACKGROUND: Ischemia/reperfusion (I/R) injury of heart is one of the major causes of acute cardiac injury, which may result in worsening or even loss of heart function. With novel microRNAs being evolutionarily discovered, numbers of them remained functionally unknown. We aimed to discover novel microRNAs with therapeutic or diagnostic potential in the setting of early cardiac I/R injury. METHODS: Cardiac electrical activity, biochemical detection and histopathology analysis were performed to reveal early changes of cardiac I/R injury. A microRNA array was performed to screen differential microRNAs in the mouse model of cardiac I/R injury. The differentially expressed microRNAs were validated in cardiac tissues and in serum samples. RESULTS: The abnormality in electrocardiogram and increases in serum cTnI levels suggested the successful establishment of cardiac I/R injury in mice. A total of 1882 microRNAs were identified, of which 11 were significantly down-regulated and 41 were significantly up-regulated at 3 h post reperfusion. microRNA 223-3p and microRNA 3113-5p were among the mostly altered microRNAs and were validated to be up-regulated within the early hours of I/R injury in heart tissues. In the circulating system, cTnI, a sensitive marker of cardiac injury, or microRNA 223-3p only increased within the first 6 h post I/R injury. However, microRNA 3113-5p stably increased in the serum, keeping an increase of 2.5-fold throughout the 24 h. In the human serum samples, microRNA 3113-5p was detected to be significantly upregulated as soon as 3 h after I/R stimuli and kept significantly higher levels within the 48 h. CONCLUSION: This is the first study that reported the functional roles of microRNA 3113-5p in cardiovascular system. Our data suggested that cardiac microRNA 3113-5p might be a useful target for therapeutic purposes and circulating microRNA 3113-5p might serve as a stable marker for early diagnosis of cardiac I/R injury. BioMed Central 2019-10-31 /pmc/articles/PMC6824141/ /pubmed/31672150 http://dx.doi.org/10.1186/s13000-019-0894-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chen, Yuanyuan
Ye, Xing
Yan, Fengping
MicroRNA 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury
title MicroRNA 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury
title_full MicroRNA 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury
title_fullStr MicroRNA 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury
title_full_unstemmed MicroRNA 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury
title_short MicroRNA 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury
title_sort microrna 3113-5p is a novel marker for early cardiac ischemia/reperfusion injury
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824141/
https://www.ncbi.nlm.nih.gov/pubmed/31672150
http://dx.doi.org/10.1186/s13000-019-0894-1
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