Investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic stroke

ObjectiveClinical associations between coronavirus disease (COVID-19) and ischemic stroke (IS) have been reported. This study aimed to investigate the shared genes between COVID-19 and IS and explore their regulatory mechanisms.MethodsPublished datasets for COVID-19 and IS were downloaded. Common di...

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Main Authors: Hao Wu, Fei Han
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-04-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2023.1151946/full
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author Hao Wu
Fei Han
author_facet Hao Wu
Fei Han
author_sort Hao Wu
collection DOAJ
description ObjectiveClinical associations between coronavirus disease (COVID-19) and ischemic stroke (IS) have been reported. This study aimed to investigate the shared genes between COVID-19 and IS and explore their regulatory mechanisms.MethodsPublished datasets for COVID-19 and IS were downloaded. Common differentially expressed genes (DEGs) in the two diseases were identified, followed by protein–protein interaction (PPI) network analysis. Moreover, overlapping module genes associated with the two diseases were investigated using weighted correlation network analysis (WGCNA). Through intersection analysis of PPI cluster genes and overlapping module genes, hub-shared genes associated with the two diseases were obtained, followed by functional enrichment analysis and external dataset validation. Moreover, the upstream miRNAs and transcription factors (TFs) of the hub-shared genes were predicted.ResultsA total of 91 common DEGs were identified from the clusters of the PPI network, and 129 overlapping module genes were screened using WGCNA. Based on further intersection analysis, four hub-shared genes in IS and COVID-19 were identified, including PDE5A, ITGB3, CEACAM8, and BPI. These hub-shared genes were remarkably enriched in pathways such as ECM-receptor interaction and focal adhesion pathways. Moreover, ITGB3, PDE5A, and CEACAM8 were targeted by 53, 32, and 3 miRNAs, respectively, and these miRNAs were also enriched in the aforementioned pathways. Furthermore, TFs, such as lactoferrin, demonstrated a stronger predicted correlation with the hub-shared genes.ConclusionThe four identified hub-shared genes may participate in crucial mechanisms underlying both COVID-19 and IS and may exhibit the potential to be biomarkers or therapeutic targets for the two diseases.
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spelling doaj.art-2ad3dfd0853c42c4aaa821bcb15a75112023-04-05T04:51:12ZengFrontiers Media S.A.Frontiers in Neurology1664-22952023-04-011410.3389/fneur.2023.11519461151946Investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic strokeHao Wu0Fei Han1Department of Anesthesiology, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Science, Beijing, ChinaDepartment of Neurology, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Science, Beijing, ChinaObjectiveClinical associations between coronavirus disease (COVID-19) and ischemic stroke (IS) have been reported. This study aimed to investigate the shared genes between COVID-19 and IS and explore their regulatory mechanisms.MethodsPublished datasets for COVID-19 and IS were downloaded. Common differentially expressed genes (DEGs) in the two diseases were identified, followed by protein–protein interaction (PPI) network analysis. Moreover, overlapping module genes associated with the two diseases were investigated using weighted correlation network analysis (WGCNA). Through intersection analysis of PPI cluster genes and overlapping module genes, hub-shared genes associated with the two diseases were obtained, followed by functional enrichment analysis and external dataset validation. Moreover, the upstream miRNAs and transcription factors (TFs) of the hub-shared genes were predicted.ResultsA total of 91 common DEGs were identified from the clusters of the PPI network, and 129 overlapping module genes were screened using WGCNA. Based on further intersection analysis, four hub-shared genes in IS and COVID-19 were identified, including PDE5A, ITGB3, CEACAM8, and BPI. These hub-shared genes were remarkably enriched in pathways such as ECM-receptor interaction and focal adhesion pathways. Moreover, ITGB3, PDE5A, and CEACAM8 were targeted by 53, 32, and 3 miRNAs, respectively, and these miRNAs were also enriched in the aforementioned pathways. Furthermore, TFs, such as lactoferrin, demonstrated a stronger predicted correlation with the hub-shared genes.ConclusionThe four identified hub-shared genes may participate in crucial mechanisms underlying both COVID-19 and IS and may exhibit the potential to be biomarkers or therapeutic targets for the two diseases.https://www.frontiersin.org/articles/10.3389/fneur.2023.1151946/fullCOVID-19ischemic strokeprotein–protein interactionweighted correlation network analysisfunctional enrichment analysis
spellingShingle Hao Wu
Fei Han
Investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic stroke
Frontiers in Neurology
COVID-19
ischemic stroke
protein–protein interaction
weighted correlation network analysis
functional enrichment analysis
title Investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic stroke
title_full Investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic stroke
title_fullStr Investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic stroke
title_full_unstemmed Investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic stroke
title_short Investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic stroke
title_sort investigation of shared genes and regulatory mechanisms associated with coronavirus disease 2019 and ischemic stroke
topic COVID-19
ischemic stroke
protein–protein interaction
weighted correlation network analysis
functional enrichment analysis
url https://www.frontiersin.org/articles/10.3389/fneur.2023.1151946/full
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AT feihan investigationofsharedgenesandregulatorymechanismsassociatedwithcoronavirusdisease2019andischemicstroke