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Macrophages-Related Genes Biomarkers in the Deterioration of Atherosclerosis

BACKGROUND: The macrophages are involved in all stages of cardiovascular diseases, demonstrating the correlation between inflammation, atherosclerosis, and myocardial infarction (MI). Here, we aim to investigate macrophages-related genes in the deterioration of atherosclerosis. METHODS: GSE41571 was...

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Autores principales: Zheng, Yue, Qi, Bingcai, Gao, Wenqing, Qi, Zhenchang, Liu, Yanwu, Wang, Yuchao, Feng, Jianyu, Cheng, Xian, Luo, Zhiqiang, Li, Tong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282674/
https://www.ncbi.nlm.nih.gov/pubmed/35845072
http://dx.doi.org/10.3389/fcvm.2022.890321
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author Zheng, Yue
Qi, Bingcai
Gao, Wenqing
Qi, Zhenchang
Liu, Yanwu
Wang, Yuchao
Feng, Jianyu
Cheng, Xian
Luo, Zhiqiang
Li, Tong
author_facet Zheng, Yue
Qi, Bingcai
Gao, Wenqing
Qi, Zhenchang
Liu, Yanwu
Wang, Yuchao
Feng, Jianyu
Cheng, Xian
Luo, Zhiqiang
Li, Tong
author_sort Zheng, Yue
collection PubMed
description BACKGROUND: The macrophages are involved in all stages of cardiovascular diseases, demonstrating the correlation between inflammation, atherosclerosis, and myocardial infarction (MI). Here, we aim to investigate macrophages-related genes in the deterioration of atherosclerosis. METHODS: GSE41571 was downloaded and the abundance of immune cells was estimated by utilizing the xCell. By utilizing the limma test and correlation analysis, differentially expressed macrophages-related genes (DEMRGs) were documented. The functional pathways and the protein–protein interaction (PPI) network were analyzed and the hub DEMRGs were obtained. The hub DEMRGs and their interactions were analyzed using NetworkAnalyst 3.0 and for validation, the expressions of hub DEMRGs were analyzed using the GSE135055 and GSE116250 datasets as well as atherosclerosis and MI mice model. RESULTS: A total of 509 differentially expressed genes (DEGs) were correlated with the abundance of macrophages and were identified as DEMRGs (Pearson correlation coefficients (PCC) > 0.6), which were mainly enriched in extracellular structure organization, lysosomal membrane, MHC protein complex binding, and so on. After screening out, 28 hub DEMRGs were obtained with degrees ≥20, including GNAI1 (degree = 113), MRPS2 (degree = 56), HCK (degree = 45), SOCS3 (degree = 40), NET1 (degree = 28), and so on. After validating using Gene Expression Omnibus (GEO) datasets and the atherosclerosis and MI mice model, eight proteins were validated using ApoE-/- and C57 mice. The expression levels of proteins, including SYNJ2, NET1, FZD7, LCP2, HCK, GNB2, and PPP4C were positively correlated to left ventricular ejection fraction (LVEF), while that of EIF4EBP1 was negatively correlated to LVEF. CONCLUSION: The screened hub DEMRGs, SYNJ2, NET1, FZD7, LCP2, HCK, GNB2, EIF4EBP1, and PPP4C, may be therapeutic targets for treatment and prediction in the patients with plaque progression and MI recurrent events. The kit of the eight hub DEMRGs may test plaque progression and MI recurrent events and help in the diagnosis and treatment of MI-induced heart failure (HF), thus decreasing mortality and morbidity.
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spelling pubmed-92826742022-07-15 Macrophages-Related Genes Biomarkers in the Deterioration of Atherosclerosis Zheng, Yue Qi, Bingcai Gao, Wenqing Qi, Zhenchang Liu, Yanwu Wang, Yuchao Feng, Jianyu Cheng, Xian Luo, Zhiqiang Li, Tong Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: The macrophages are involved in all stages of cardiovascular diseases, demonstrating the correlation between inflammation, atherosclerosis, and myocardial infarction (MI). Here, we aim to investigate macrophages-related genes in the deterioration of atherosclerosis. METHODS: GSE41571 was downloaded and the abundance of immune cells was estimated by utilizing the xCell. By utilizing the limma test and correlation analysis, differentially expressed macrophages-related genes (DEMRGs) were documented. The functional pathways and the protein–protein interaction (PPI) network were analyzed and the hub DEMRGs were obtained. The hub DEMRGs and their interactions were analyzed using NetworkAnalyst 3.0 and for validation, the expressions of hub DEMRGs were analyzed using the GSE135055 and GSE116250 datasets as well as atherosclerosis and MI mice model. RESULTS: A total of 509 differentially expressed genes (DEGs) were correlated with the abundance of macrophages and were identified as DEMRGs (Pearson correlation coefficients (PCC) > 0.6), which were mainly enriched in extracellular structure organization, lysosomal membrane, MHC protein complex binding, and so on. After screening out, 28 hub DEMRGs were obtained with degrees ≥20, including GNAI1 (degree = 113), MRPS2 (degree = 56), HCK (degree = 45), SOCS3 (degree = 40), NET1 (degree = 28), and so on. After validating using Gene Expression Omnibus (GEO) datasets and the atherosclerosis and MI mice model, eight proteins were validated using ApoE-/- and C57 mice. The expression levels of proteins, including SYNJ2, NET1, FZD7, LCP2, HCK, GNB2, and PPP4C were positively correlated to left ventricular ejection fraction (LVEF), while that of EIF4EBP1 was negatively correlated to LVEF. CONCLUSION: The screened hub DEMRGs, SYNJ2, NET1, FZD7, LCP2, HCK, GNB2, EIF4EBP1, and PPP4C, may be therapeutic targets for treatment and prediction in the patients with plaque progression and MI recurrent events. The kit of the eight hub DEMRGs may test plaque progression and MI recurrent events and help in the diagnosis and treatment of MI-induced heart failure (HF), thus decreasing mortality and morbidity. Frontiers Media S.A. 2022-06-30 /pmc/articles/PMC9282674/ /pubmed/35845072 http://dx.doi.org/10.3389/fcvm.2022.890321 Text en Copyright © 2022 Zheng, Qi, Gao, Qi, Liu, Wang, Feng, Cheng, Luo and Li. 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 Cardiovascular Medicine
Zheng, Yue
Qi, Bingcai
Gao, Wenqing
Qi, Zhenchang
Liu, Yanwu
Wang, Yuchao
Feng, Jianyu
Cheng, Xian
Luo, Zhiqiang
Li, Tong
Macrophages-Related Genes Biomarkers in the Deterioration of Atherosclerosis
title Macrophages-Related Genes Biomarkers in the Deterioration of Atherosclerosis
title_full Macrophages-Related Genes Biomarkers in the Deterioration of Atherosclerosis
title_fullStr Macrophages-Related Genes Biomarkers in the Deterioration of Atherosclerosis
title_full_unstemmed Macrophages-Related Genes Biomarkers in the Deterioration of Atherosclerosis
title_short Macrophages-Related Genes Biomarkers in the Deterioration of Atherosclerosis
title_sort macrophages-related genes biomarkers in the deterioration of atherosclerosis
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282674/
https://www.ncbi.nlm.nih.gov/pubmed/35845072
http://dx.doi.org/10.3389/fcvm.2022.890321
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