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pmid:38022551

Bioinformatics analyses of gene expression profile to identify pathogenic mechanisms for COVID-19 infection and cutaneous lupus erythematosus.

Zhenyu Gao · Xinchao Zhai · Guoqing Yan · Yao Tian · Xia Huang · Qingchao Wu · Lin Yuan · Linchong Su

Frontiers in immunology · 2023 doi:10.3389/fimmu.2023.1268912

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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title
Bioinformatics analyses of gene expression profile to identify pathogenic mechanisms for COVID-19 infection and cutaneous lupus erythematosus.
doi
10.3389/fimmu.2023.1268912
pmid
38022551
authors array · 8 items
[0]
Zhenyu Gao
[1]
Xinchao Zhai
[2]
Guoqing Yan
[3]
Yao Tian
[4]
Xia Huang
[5]
Qingchao Wu
[6]
Lin Yuan
[7]
Linchong Su
journal
Frontiers in immunology
year
2023
abstract
Objective: The global mortality rates have surged due to the ongoing coronavirus disease 2019 (COVID-19), leading to a worldwide catastrophe. Increasing incidents of patients suffering from cutaneous lupus erythematosus (CLE) exacerbations after either contracting COVID-19 or getting immunized against it, have been observed in recent research. However, the precise intricacies that prompt this unexpected complication are yet to be fully elucidated. This investigation seeks to probe into the molecular events inciting this adverse outcome. Method: Gene expression patterns from the Gene Expression Omnibus (GEO) database, specifically GSE171110 and GSE109248, were extracted. We then discovered common differentially expressed genes (DEGs) in both COVID-19 and CLE. This led to the creation of functional annotations, formation of a protein-protein interaction (PPI) network, and identification of key genes. Furthermore, regulatory networks relating to these shared DEGs and significant genes were constructed. Result: We identified 214 overlapping DEGs in both COVID-19 and CLE datasets. The following functional enrichment analysis of these DEGs highlighted a significant enrichment in pathways related to virus response and infectious disease in both conditions. Next, a PPI network was constructed using bioinformatics tools, resulting in the identification of 5 hub genes. Finally, essential regulatory networks including transcription factor-gene and miRNA-gene interactions were determined. Conclusion: Our findings demonstrate shared pathogenesis between COVID-19 and CLE, offering potential insights for future mechanistic investigations. And the identification of common pathways and key genes in these conditions may provide novel avenues for research.
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In our quest to identify the DEGs separating COVID-19 and HC subjects within the GSE171110 dataset, we adopted the use of limma packages within the R programming language.
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/geo/under the accession numbers GSE109248/GSE171110.
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We identified 214 overlapping DEGs in both COVID-19 and CLE datasets.
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We identified 214 overlapping DEGs in both COVID-19 and CLE datasets.
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Genome-wide analysis of gene expression of cutaneous lupus and cutaneous psoriasis lesions
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38022551", "kind": "science-record", "revision": 4, "content_hash": "sha256:c61a8463816ca4240aaee0a51dd423569836eced9e4a64b7c46a480bed4c4303", "created_at": "2026-11-01T19:02:56Z", "updated_at": "2026-11-01T22:53:10Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Bioinformatics analyses of gene expression profile to identify pathogenic mechanisms for COVID-19 infection and cutaneous lupus erythematosus.", "doi": "10.3389/fimmu.2023.1268912", "pmid": "38022551", "authors": ["Zhenyu Gao", "Xinchao Zhai", "Guoqing Yan", "Yao Tian", "Xia Huang", "Qingchao Wu", "Lin Yuan", "Linchong Su"], "journal": "Frontiers in immunology", "year": 2023, "abstract": "Objective: The global mortality rates have surged due to the ongoing coronavirus disease 2019 (COVID-19), leading to a worldwide catastrophe. Increasing incidents of patients suffering from cutaneous lupus erythematosus (CLE) exacerbations after either contracting COVID-19 or getting immunized against it, have been observed in recent research. However, the precise intricacies that prompt this unexpected complication are yet to be fully elucidated. This investigation seeks to probe into the molecular events inciting this adverse outcome.\nMethod: Gene expression patterns from the Gene Expression Omnibus (GEO) database, specifically GSE171110 and GSE109248, were extracted. We then discovered common differentially expressed genes (DEGs) in both COVID-19 and CLE. This led to the creation of functional annotations, formation of a protein-protein interaction (PPI) network, and identification of key genes. Furthermore, regulatory networks relating to these shared DEGs and significant genes were constructed.\nResult: We identified 214 overlapping DEGs in both COVID-19 and CLE datasets. The following functional enrichment analysis of these DEGs highlighted a significant enrichment in pathways related to virus response and infectious disease in both conditions. Next, a PPI network was constructed using bioinformatics tools, resulting in the identification of 5 hub genes. Finally, essential regulatory networks including transcription factor-gene and miRNA-gene interactions were determined.\nConclusion: Our findings demonstrate shared pathogenesis between COVID-19 and CLE, offering potential insights for future mechanistic investigations. 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