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pmid:35128085

Common genetic aspects between COVID-19 and sarcoidosis: A network-based approach using gene expression data.

Md Roman Mogal · Sagarika Adhikary Sompa · Asadullah Junayed · Md Rashel Mahmod · Md Zainul Abedin · Md Asaduzzaman Sikder

Biochemistry and biophysics reports · 2022 doi:10.1016/j.bbrep.2022.101219

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35128085
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science-record
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2026-11-01T17:36:53Z
updated_at
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state
complete
title
Common genetic aspects between COVID-19 and sarcoidosis: A network-based approach using gene expression data.
doi
10.1016/j.bbrep.2022.101219
pmid
35128085
authors array · 6 items
[0]
Md Roman Mogal
[1]
Sagarika Adhikary Sompa
[2]
Asadullah Junayed
[3]
Md Rashel Mahmod
[4]
Md Zainul Abedin
[5]
Md Asaduzzaman Sikder
journal
Biochemistry and biophysics reports
year
2022
abstract
The pandemic situation of novel coronavirus disease 2019 (COVID-19) is a global threat on our current planet, with its rapid spread and high mortality rate. Sarcoidosis patients are at high risk to COVID-19 severity for having lung injuries as well as treating with immunosuppressive agents. So, physicians are in dilemma whether they should use immunosuppressive agents or not for the patients with sarcoidosis history and COVID-19 infection. Therefore, common factors should be identified to provide effective treatment. For determining the common genes between COVID-19 and sarcoidosis, GSE164805 and GSE18781 were retrieved from the Gene Expression Omnibus (GEO) database. Common upregulated genes were identified by using R language to investigate their involved pathways and gene ontologies (GO). With the aid of the STRING Cytoscape plugin tool, protein-protein interactions (PPIs) network was constructed. From the PPIs network, Hub genes and essential modules were detected by using Cytohubba, and MCODE respectively. For hub genes, TFs, TFs-miRNA, and drug, interaction networks were built through the NetworkAnalyst web platform. A total of 34 common upregulated genes were identified and among them, five hub genes, including TET2, MUC5AC, VDR, NFE2L2, and BCL6 were determined. In addition, a cluster having VDR and NFE2L2 was detected from the PPIs network. Moreover, 32 transcription factors and 9 miRNA were recognized for hub genes. Furthermore, vitamin D and some of its analogous compounds were obtained from the drug interaction network. In conclusion, hub genes identified in this study might have potential roles in modulating COVID-19 infection and sarcoidosis. However, further studies are required to corroborate this study.
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For identifying common differentially expressed genes (DEGs) from both datasets, GEO2R (https://www.ncbi.nlm.nih.gov/geo/geo2r/) was applied. GEO2R is used to identify DEGs, using GEOquery and limma R packages from the Bioconductor project, having compared two or more groups of samples [16]. In order to control the false discovery rate, Benjamini-Hochberg was conducted [17].
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sections[4] "Identification of common upregulated genes" paragraph 2
quote
For identifying common differentially expressed genes (DEGs) from both datasets, GEO2R (https://www.ncbi.nlm.nih.gov/geo/geo2r/) was applied. GEO2R is used to identify DEGs, using GEOquery and limma R packages from the Bioconductor project, having compared two or more groups of samples [16]. In order to control the false discovery rate, Benjamini-Hochberg was conducted [17].
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sections[25] "Data availability" paragraph 2
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No data was used for the research described in the article.
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The study identified 34 common upregulated genes between COVID-19 and sarcoidosis and five hub genes: TET2, MUC5AC, VDR, NFE2L2, and BCL6.
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sections[0] "Abstract" paragraph 1
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A total of 34 common upregulated genes were identified and among them, five hub genes, including TET2, MUC5AC, VDR, NFE2L2, and BCL6 were determined.
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sections[0] "Abstract" paragraph 5
quote
34 common upregulated genes were identified from GSE164805 and GSE18781 datasets.
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The study identified 34 common upregulated genes between COVID-19 and sarcoidosis and five hub genes: TET2, MUC5AC, VDR, NFE2L2, and BCL6.
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The transcriptional profiles of severe COVID-19
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GSM465934
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GSM465935
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GSM465936
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GSM465937
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GSM465941
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GSM465942
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GSM465944
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GSM465946
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GSM465951
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GSM465956
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GSM465957
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GSM465958
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GSM465959
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GSM465960
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GSM465961
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55
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570
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Homo sapiens
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Gene Expression in Inflammatory Diseases
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For identifying common differentially expressed genes (DEGs) from both datasets, GEO2R (https://www.ncbi.nlm.nih.gov/geo/geo2r/) was applied. GEO2R is used to identify DEGs, using GEOquery and limma R packages from the Bioconductor project, having compared two or more groups of samples [16]. In order to control the false discovery rate, Benjamini-Hochberg was conducted [17].
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Sarcoidosis patients are at high risk to COVID-19 severity for having lung injuries as well as treating with immunosuppressive agents. So, physicians are in dilemma whether they should use immunosuppressive agents or not for the patients with sarcoidosis history and COVID-19 infection. Therefore, common factors should be identified to provide effective treatment. For determining the common genes between COVID-19 and sarcoidosis, GSE164805 and GSE18781 were retrieved from the Gene Expression Omnibus (GEO) database. Common upregulated genes were identified by using R language to investigate their involved pathways and gene ontologies (GO). With the aid of the STRING Cytoscape plugin tool, protein-protein interactions (PPIs) network was constructed. From the PPIs network, Hub genes and essential modules were detected by using Cytohubba, and MCODE respectively. For hub genes, TFs, TFs-miRNA, and drug, interaction networks were built through the NetworkAnalyst web platform. A total of 34 common upregulated genes were identified and among them, five hub genes, including TET2, MUC5AC, VDR, NFE2L2, and BCL6 were determined. In addition, a cluster having VDR and NFE2L2 was detected from the PPIs network. Moreover, 32 transcription factors and 9 miRNA were recognized for hub genes. Furthermore, vitamin D and some of its analogous compounds were obtained from the drug interaction network. In conclusion, hub genes identified in this study might have potential roles in modulating COVID-19 infection and sarcoidosis. However, further studies are required to corroborate this study.", "claims": [{"id": "claim-method", "statement": "For identifying common differentially expressed genes (DEGs) from both datasets, GEO2R (https://www.ncbi.nlm.nih.gov/geo/geo2r/) was applied. GEO2R is used to identify DEGs, using GEOquery and limma R packages from the Bioconductor project, having compared two or more groups of samples [16]. 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