Serum Exosomal MicroRNA-21, MicroRNA-126, and PTEN Are Novel Biomarkers for Diagnosis of Acute Coronary Syndrome

Acute coronary syndrome (ACS) is a serious threat to public health. Based on clinical manifestations, ACS can be classified into unstable angina (UA) pectoris and acute myocardial infarction (AMI). The purpose of this study was to explore the possibility of using serum exosomal microRNA (miR)-126, m...

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Main Authors: Hao Ling, Ziyuan Guo, Yongfeng Shi, Lei Zhang, Chunli Song
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-06-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphys.2020.00654/full
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spelling doaj-f6183cfb11b94cfcbe6b8aa486b1a6c72020-11-25T03:34:22ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2020-06-011110.3389/fphys.2020.00654524775Serum Exosomal MicroRNA-21, MicroRNA-126, and PTEN Are Novel Biomarkers for Diagnosis of Acute Coronary SyndromeHao Ling0Ziyuan Guo1Yongfeng Shi2Lei Zhang3Chunli Song4Department of Cardiology, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Cardiology, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Cardiology, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Neurology, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Cardiology, The Second Hospital of Jilin University, Changchun, ChinaAcute coronary syndrome (ACS) is a serious threat to public health. Based on clinical manifestations, ACS can be classified into unstable angina (UA) pectoris and acute myocardial infarction (AMI). The purpose of this study was to explore the possibility of using serum exosomal microRNA (miR)-126, miR-21, and phosphatase and tensin homolog (PTEN) expression levels as biomarkers of UA and AMI and to investigate whether these levels were positively correlated with the severity of coronary stenosis based on the Gensini score. Exosomes were isolated by ultracentrifugation from the serum of 34 patients with AMI, 31 patients with UA, and 22 healthy controls. The isolated exosomes were characterized by electron microscopy and particle size analysis; exosomal identity was further confirmed by western blotting using exosome-specific antibodies. Real-time quantitative polymerase chain reaction indicated that the serum exosomal levels of miR-126 and miR-21 were significantly higher in the patients with UA and AMI than in the healthy controls. Enzyme-linked immunosorbent assay showed that the serum exosomal PTEN levels were significantly higher in the UA and AMI groups than in the control group. Receiving operating characteristic curve analysis demonstrated the diagnostic efficiency of serum exosomal miR-126, miR-21, and PTEN levels for predicting AMI and UA. In addition, the circulating exosomal miR-126 level was positively correlated with the severity of coronary artery stenosis in patients with UA and AMI based on the Gensini score.https://www.frontiersin.org/article/10.3389/fphys.2020.00654/fullexosomal miRNA-126exosomal miRNA-21PTENcoronary heart diseaseacute coronary syndromebiomarker severity
collection DOAJ
language English
format Article
sources DOAJ
author Hao Ling
Ziyuan Guo
Yongfeng Shi
Lei Zhang
Chunli Song
spellingShingle Hao Ling
Ziyuan Guo
Yongfeng Shi
Lei Zhang
Chunli Song
Serum Exosomal MicroRNA-21, MicroRNA-126, and PTEN Are Novel Biomarkers for Diagnosis of Acute Coronary Syndrome
Frontiers in Physiology
exosomal miRNA-126
exosomal miRNA-21
PTEN
coronary heart disease
acute coronary syndrome
biomarker severity
author_facet Hao Ling
Ziyuan Guo
Yongfeng Shi
Lei Zhang
Chunli Song
author_sort Hao Ling
title Serum Exosomal MicroRNA-21, MicroRNA-126, and PTEN Are Novel Biomarkers for Diagnosis of Acute Coronary Syndrome
title_short Serum Exosomal MicroRNA-21, MicroRNA-126, and PTEN Are Novel Biomarkers for Diagnosis of Acute Coronary Syndrome
title_full Serum Exosomal MicroRNA-21, MicroRNA-126, and PTEN Are Novel Biomarkers for Diagnosis of Acute Coronary Syndrome
title_fullStr Serum Exosomal MicroRNA-21, MicroRNA-126, and PTEN Are Novel Biomarkers for Diagnosis of Acute Coronary Syndrome
title_full_unstemmed Serum Exosomal MicroRNA-21, MicroRNA-126, and PTEN Are Novel Biomarkers for Diagnosis of Acute Coronary Syndrome
title_sort serum exosomal microrna-21, microrna-126, and pten are novel biomarkers for diagnosis of acute coronary syndrome
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2020-06-01
description Acute coronary syndrome (ACS) is a serious threat to public health. Based on clinical manifestations, ACS can be classified into unstable angina (UA) pectoris and acute myocardial infarction (AMI). The purpose of this study was to explore the possibility of using serum exosomal microRNA (miR)-126, miR-21, and phosphatase and tensin homolog (PTEN) expression levels as biomarkers of UA and AMI and to investigate whether these levels were positively correlated with the severity of coronary stenosis based on the Gensini score. Exosomes were isolated by ultracentrifugation from the serum of 34 patients with AMI, 31 patients with UA, and 22 healthy controls. The isolated exosomes were characterized by electron microscopy and particle size analysis; exosomal identity was further confirmed by western blotting using exosome-specific antibodies. Real-time quantitative polymerase chain reaction indicated that the serum exosomal levels of miR-126 and miR-21 were significantly higher in the patients with UA and AMI than in the healthy controls. Enzyme-linked immunosorbent assay showed that the serum exosomal PTEN levels were significantly higher in the UA and AMI groups than in the control group. Receiving operating characteristic curve analysis demonstrated the diagnostic efficiency of serum exosomal miR-126, miR-21, and PTEN levels for predicting AMI and UA. In addition, the circulating exosomal miR-126 level was positively correlated with the severity of coronary artery stenosis in patients with UA and AMI based on the Gensini score.
topic exosomal miRNA-126
exosomal miRNA-21
PTEN
coronary heart disease
acute coronary syndrome
biomarker severity
url https://www.frontiersin.org/article/10.3389/fphys.2020.00654/full
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