Regulatory T Cell-Related Gene Biomarkers in the Deterioration of Atherosclerosis
Background: Regulatory T cells (Tregs) have shown to be protective against the development of atherosclerosis, a major pathological cause for cardiovascular events. Here, we aim to explore the roles of Tregs-related genes in atherosclerosis deterioration.Methods and Results: We downloaded the gene e...
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2021-05-01
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doaj-5953914cb5a749d1a18bae1d6d399fe82021-05-20T04:20:20ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2021-05-01810.3389/fcvm.2021.661709661709Regulatory T Cell-Related Gene Biomarkers in the Deterioration of AtherosclerosisMeng Xia0Qingmeng Wu1Pengfei Chen2Cheng Qian3Department of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, ChinaHealthcare-Associated Infections Control Center, The Affiliated Chinese Medicine Hospital of Southwest Medical University, Luzhou, ChinaDepartment of Gastroenterology, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, ChinaDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, ChinaBackground: Regulatory T cells (Tregs) have shown to be protective against the development of atherosclerosis, a major pathological cause for cardiovascular events. Here, we aim to explore the roles of Tregs-related genes in atherosclerosis deterioration.Methods and Results: We downloaded the gene expression profile of 29 atherosclerotic samples from the Gene Expression Omnibus database with an accession number of GSE28829. The abundance of Tregs estimated by the CIBERSORT algorithm was negatively correlated with the atherosclerotic stage. Using the limma test and correlation analysis, a total of 159 differentially expressed Tregs-related genes (DETregRGs) between early and advanced atherosclerotic plaques were documented. Functional annotation analysis using the DAVID tool indicated that the DETregRGs were mainly enriched in inflammatory responses, immune-related mechanisms, and pathways such as complement and coagulation cascades, platelet activation, leukocyte trans-endothelial migration, vascular smooth muscle contraction, and so on. A protein-protein interaction network of the DETregRGs was then constructed, and five hub genes (PTPRC, C3AR1, CD53, TLR2, and CCR1) were derived from the network with node degrees ≥20. The expression patterns of these hub DETregRGs were further validated in several independent datasets. Finally, a single sample scoring method was used to build a gene signature for the five DETregRGs, which could distinguish patients with myocardial infarction from those with stable coronary disease.Conclusion: The results of this study will improve our understanding about the Tregs-associated molecular mechanisms in the progression of atherosclerosis and facilitate the discovery of novel biomarkers for acute cardiovascular events.https://www.frontiersin.org/articles/10.3389/fcvm.2021.661709/fullregulatory T cellsatherosclerosisprogressionbiological networkgenes |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Meng Xia Qingmeng Wu Pengfei Chen Cheng Qian |
spellingShingle |
Meng Xia Qingmeng Wu Pengfei Chen Cheng Qian Regulatory T Cell-Related Gene Biomarkers in the Deterioration of Atherosclerosis Frontiers in Cardiovascular Medicine regulatory T cells atherosclerosis progression biological network genes |
author_facet |
Meng Xia Qingmeng Wu Pengfei Chen Cheng Qian |
author_sort |
Meng Xia |
title |
Regulatory T Cell-Related Gene Biomarkers in the Deterioration of Atherosclerosis |
title_short |
Regulatory T Cell-Related Gene Biomarkers in the Deterioration of Atherosclerosis |
title_full |
Regulatory T Cell-Related Gene Biomarkers in the Deterioration of Atherosclerosis |
title_fullStr |
Regulatory T Cell-Related Gene Biomarkers in the Deterioration of Atherosclerosis |
title_full_unstemmed |
Regulatory T Cell-Related Gene Biomarkers in the Deterioration of Atherosclerosis |
title_sort |
regulatory t cell-related gene biomarkers in the deterioration of atherosclerosis |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cardiovascular Medicine |
issn |
2297-055X |
publishDate |
2021-05-01 |
description |
Background: Regulatory T cells (Tregs) have shown to be protective against the development of atherosclerosis, a major pathological cause for cardiovascular events. Here, we aim to explore the roles of Tregs-related genes in atherosclerosis deterioration.Methods and Results: We downloaded the gene expression profile of 29 atherosclerotic samples from the Gene Expression Omnibus database with an accession number of GSE28829. The abundance of Tregs estimated by the CIBERSORT algorithm was negatively correlated with the atherosclerotic stage. Using the limma test and correlation analysis, a total of 159 differentially expressed Tregs-related genes (DETregRGs) between early and advanced atherosclerotic plaques were documented. Functional annotation analysis using the DAVID tool indicated that the DETregRGs were mainly enriched in inflammatory responses, immune-related mechanisms, and pathways such as complement and coagulation cascades, platelet activation, leukocyte trans-endothelial migration, vascular smooth muscle contraction, and so on. A protein-protein interaction network of the DETregRGs was then constructed, and five hub genes (PTPRC, C3AR1, CD53, TLR2, and CCR1) were derived from the network with node degrees ≥20. The expression patterns of these hub DETregRGs were further validated in several independent datasets. Finally, a single sample scoring method was used to build a gene signature for the five DETregRGs, which could distinguish patients with myocardial infarction from those with stable coronary disease.Conclusion: The results of this study will improve our understanding about the Tregs-associated molecular mechanisms in the progression of atherosclerosis and facilitate the discovery of novel biomarkers for acute cardiovascular events. |
topic |
regulatory T cells atherosclerosis progression biological network genes |
url |
https://www.frontiersin.org/articles/10.3389/fcvm.2021.661709/full |
work_keys_str_mv |
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