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MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort

The aim of this study was to investigate the expression of circulating microRNAs (miRNAs) in apolipoprotein E (apoE) knockout mice (apoE(−/−)) and to validate the role of these miRNAs in human coronary artery disease (CAD). Pooled plasma from 10 apoE(−/−) mice and 10 healthy C57BL/6 (B6) mice was us...

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Autores principales: Han, Hui, Qu, Guangjin, Han, Chenghua, Wang, Yuhong, Sun, Tingting, Li, Fengqing, Wang, Junxiao, Luo, Shanshun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346489/
https://www.ncbi.nlm.nih.gov/pubmed/25656948
http://dx.doi.org/10.1038/emm.2014.81
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author Han, Hui
Qu, Guangjin
Han, Chenghua
Wang, Yuhong
Sun, Tingting
Li, Fengqing
Wang, Junxiao
Luo, Shanshun
author_facet Han, Hui
Qu, Guangjin
Han, Chenghua
Wang, Yuhong
Sun, Tingting
Li, Fengqing
Wang, Junxiao
Luo, Shanshun
author_sort Han, Hui
collection PubMed
description The aim of this study was to investigate the expression of circulating microRNAs (miRNAs) in apolipoprotein E (apoE) knockout mice (apoE(−/−)) and to validate the role of these miRNAs in human coronary artery disease (CAD). Pooled plasma from 10 apoE(−/−) mice and 10 healthy C57BL/6 (B6) mice was used to perform the microarray analysis. The results showed that miR-34a, miR-21, miR-23a, miR-30a and miR-106b were differentially expressed in apoE(−/−) mice, and these expression changes were confirmed by real-time quantitative reverse-transcription PCR. Then, miR-34a, miR-21, miR-23a, miR-30a and miR-106b were detected in the plasma of 32 patients with CAD and of 20 healthy controls. Only miR-34a, miR-21 and miR-23a were significantly differentially expressed in the plasma of CAD patients (all P<0.01). In conclusion, miR-34a, miR-21 and miR-23a were elevated in CAD patients, which means that these miRNAs might serve as biomarkers of CAD development and progression.
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spelling pubmed-43464892015-03-04 MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort Han, Hui Qu, Guangjin Han, Chenghua Wang, Yuhong Sun, Tingting Li, Fengqing Wang, Junxiao Luo, Shanshun Exp Mol Med Original Article The aim of this study was to investigate the expression of circulating microRNAs (miRNAs) in apolipoprotein E (apoE) knockout mice (apoE(−/−)) and to validate the role of these miRNAs in human coronary artery disease (CAD). Pooled plasma from 10 apoE(−/−) mice and 10 healthy C57BL/6 (B6) mice was used to perform the microarray analysis. The results showed that miR-34a, miR-21, miR-23a, miR-30a and miR-106b were differentially expressed in apoE(−/−) mice, and these expression changes were confirmed by real-time quantitative reverse-transcription PCR. Then, miR-34a, miR-21, miR-23a, miR-30a and miR-106b were detected in the plasma of 32 patients with CAD and of 20 healthy controls. Only miR-34a, miR-21 and miR-23a were significantly differentially expressed in the plasma of CAD patients (all P<0.01). In conclusion, miR-34a, miR-21 and miR-23a were elevated in CAD patients, which means that these miRNAs might serve as biomarkers of CAD development and progression. Nature Publishing Group 2015-02 2015-02-06 /pmc/articles/PMC4346489/ /pubmed/25656948 http://dx.doi.org/10.1038/emm.2014.81 Text en Copyright © 2015 KSBMB. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Original Article
Han, Hui
Qu, Guangjin
Han, Chenghua
Wang, Yuhong
Sun, Tingting
Li, Fengqing
Wang, Junxiao
Luo, Shanshun
MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort
title MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort
title_full MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort
title_fullStr MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort
title_full_unstemmed MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort
title_short MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort
title_sort mir-34a, mir-21 and mir-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346489/
https://www.ncbi.nlm.nih.gov/pubmed/25656948
http://dx.doi.org/10.1038/emm.2014.81
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