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Exploring the Role of Epicardial Adipose Tissue in Coronary Artery Disease From the Difference of Gene Expression
OBJECTIVES: Epicardial adipose tissue (EAT) is closely adjacent to the coronary arteries and myocardium, its role as an endocrine organ to affect the pathophysiological processes of the coronary arteries and myocardium has been increasingly recognized. However, the specific gene expression profiles...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042318/ https://www.ncbi.nlm.nih.gov/pubmed/33859569 http://dx.doi.org/10.3389/fphys.2021.605811 |
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author | Wang, Qian-Chen Wang, Zhen-Yu Xu, Qian Li, Ruo-Bing Zhang, Guo-Gang Shi, Rui-Zheng |
author_facet | Wang, Qian-Chen Wang, Zhen-Yu Xu, Qian Li, Ruo-Bing Zhang, Guo-Gang Shi, Rui-Zheng |
author_sort | Wang, Qian-Chen |
collection | PubMed |
description | OBJECTIVES: Epicardial adipose tissue (EAT) is closely adjacent to the coronary arteries and myocardium, its role as an endocrine organ to affect the pathophysiological processes of the coronary arteries and myocardium has been increasingly recognized. However, the specific gene expression profiles of EAT in coronary artery disease (CAD) has not been well characterized. Our aim was to investigate the role of EAT in CAD at the gene level. METHODS: Here, we compared the histological and gene expression difference of EAT between CAD and non-CAD. We investigated the gene expression profiles in the EAT of patients with CAD through the high-throughput RNA sequencing. We performed bioinformatics analysis such as functional enrichment analysis and protein-protein interaction network construction to obtain and verify the hub differentially expressed genes (DEGs) in the EAT of CAD. RESULTS: Our results showed that the size of epicardial adipocytes in the CAD group was larger than in the control group. Our findings on the EAT gene expression profiles of CAD showed a total of 747 DEGs (fold change >2, p value <0.05). The enrichment analysis of DEGs showed that more pro-inflammatory and immunological genes and pathways were involved in CAD. Ten hub DEGs (GNG3, MCHR1, BDKRB1, MCHR2, CXCL8, CXCR5, CCR8, CCL4L1, TAS2R10, and TAS2R41) were identified. CONCLUSION: Epicardial adipose tissue in CAD shows unique gene expression profiles and may act as key regulators in the CAD pathological process. |
format | Online Article Text |
id | pubmed-8042318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80423182021-04-14 Exploring the Role of Epicardial Adipose Tissue in Coronary Artery Disease From the Difference of Gene Expression Wang, Qian-Chen Wang, Zhen-Yu Xu, Qian Li, Ruo-Bing Zhang, Guo-Gang Shi, Rui-Zheng Front Physiol Physiology OBJECTIVES: Epicardial adipose tissue (EAT) is closely adjacent to the coronary arteries and myocardium, its role as an endocrine organ to affect the pathophysiological processes of the coronary arteries and myocardium has been increasingly recognized. However, the specific gene expression profiles of EAT in coronary artery disease (CAD) has not been well characterized. Our aim was to investigate the role of EAT in CAD at the gene level. METHODS: Here, we compared the histological and gene expression difference of EAT between CAD and non-CAD. We investigated the gene expression profiles in the EAT of patients with CAD through the high-throughput RNA sequencing. We performed bioinformatics analysis such as functional enrichment analysis and protein-protein interaction network construction to obtain and verify the hub differentially expressed genes (DEGs) in the EAT of CAD. RESULTS: Our results showed that the size of epicardial adipocytes in the CAD group was larger than in the control group. Our findings on the EAT gene expression profiles of CAD showed a total of 747 DEGs (fold change >2, p value <0.05). The enrichment analysis of DEGs showed that more pro-inflammatory and immunological genes and pathways were involved in CAD. Ten hub DEGs (GNG3, MCHR1, BDKRB1, MCHR2, CXCL8, CXCR5, CCR8, CCL4L1, TAS2R10, and TAS2R41) were identified. CONCLUSION: Epicardial adipose tissue in CAD shows unique gene expression profiles and may act as key regulators in the CAD pathological process. Frontiers Media S.A. 2021-03-30 /pmc/articles/PMC8042318/ /pubmed/33859569 http://dx.doi.org/10.3389/fphys.2021.605811 Text en Copyright © 2021 Wang, Wang, Xu, Li, Zhang and Shi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Wang, Qian-Chen Wang, Zhen-Yu Xu, Qian Li, Ruo-Bing Zhang, Guo-Gang Shi, Rui-Zheng Exploring the Role of Epicardial Adipose Tissue in Coronary Artery Disease From the Difference of Gene Expression |
title | Exploring the Role of Epicardial Adipose Tissue in Coronary Artery Disease From the Difference of Gene Expression |
title_full | Exploring the Role of Epicardial Adipose Tissue in Coronary Artery Disease From the Difference of Gene Expression |
title_fullStr | Exploring the Role of Epicardial Adipose Tissue in Coronary Artery Disease From the Difference of Gene Expression |
title_full_unstemmed | Exploring the Role of Epicardial Adipose Tissue in Coronary Artery Disease From the Difference of Gene Expression |
title_short | Exploring the Role of Epicardial Adipose Tissue in Coronary Artery Disease From the Difference of Gene Expression |
title_sort | exploring the role of epicardial adipose tissue in coronary artery disease from the difference of gene expression |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042318/ https://www.ncbi.nlm.nih.gov/pubmed/33859569 http://dx.doi.org/10.3389/fphys.2021.605811 |
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