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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4346489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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