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

被引:1
|
作者
Gao, Zhenyu [1 ,2 ]
Zhai, Xinchao [1 ,2 ]
Yan, Guoqing [1 ,2 ]
Tian, Yao [1 ,2 ]
Huang, Xia [1 ,2 ]
Wu, Qingchao [1 ,2 ]
Yuan, Lin [1 ]
Su, Linchong [1 ,2 ]
机构
[1] Hubei Minzu Univ, Hubei Prov Key Lab Occurrence & Intervent Rheumat, Minda Hosp, Enshi, Peoples R China
[2] Hubei Minzu Univ, Minda Hosp, Dept Rheumatol & Immunol, Enshi, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
COVID-19; cutaneous lupus erythematosus; differentially expressed genes; regulatory network; pathogenic mechanisms; SKIN; ASSOCIATION; DIFFERENTIATION; DERMATOMYOSITIS; ACTIVATION; PROTEIN; MDA5;
D O I
10.3389/fimmu.2023.1268912
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
ObjectiveThe 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.MethodGene 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.ResultWe 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.ConclusionOur 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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页数:11
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