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pmid:36059966

Exploring the pathogenesis of diabetic kidney disease by microarray data analysis.

Haiyan Cao · Xiaosheng Rao · Junya Jia · Tiekun Yan · Dong Li

Frontiers in pharmacology · 2022 doi:10.3389/fphar.2022.932205

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

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title
Exploring the pathogenesis of diabetic kidney disease by microarray data analysis.
doi
10.3389/fphar.2022.932205
pmid
36059966
authors array · 5 items
[0]
Haiyan Cao
[1]
Xiaosheng Rao
[2]
Junya Jia
[3]
Tiekun Yan
[4]
Dong Li
journal
Frontiers in pharmacology
year
2022
abstract
Diabetic kidney disease (DKD) is a major complication of diabetes mellitus, and the leading contributor of end-stage renal disease. Hence, insights into the molecular pathogenesis of DKD are urgently needed. The purpose of this article is to reveal the molecular mechanisms underlying the pathogenesis of DKD. The microarray datasets of GSE30528 and GSE30529 were downloaded from the NCBI Gene Expression Omnibus (GEO) database to identify the common differentially expressed genes (DEGs) between the glomerular DKD (GDKD) and tubular DKD (TDKD), respectively. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were performed to analyze the function and pathways of the common DEGs. After constructing the protein-protein interaction (PPI) network and subnetwork analysis, three types of analyses were performed, namely, identification of hub genes, analysis of the coexpressed network, and exploration of transcription factors (TFs). Totally, 348 and 463 DEGs were identified in GDKD and TDKD, respectively. Then, 66 common DEGs (63 upregulated DEGs and three downregulated DEGs) were obtained in DKD patients. GO and KEGG pathway analyses revealed the importance of inflammation response, immune-related pathways, and extracellular matrix-related pathways, especially chemokines and cytokines, in DKD. Fifteen hub genes from the 66 common DEGs, namely, IL10RA, IRF8, LY86, C1QA, C1QB, CD53, CD1C, CTSS, CCR2, CD163, CCL5, CD48, RNASE6, CD52, and CD2 were identified. In summary, through the microarray data analysis, the common functions and hub genes greatly contribute to the elucidation of the molecular pathogenesis associated with DKD.
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Based on the GEOquery package and Limma package of R software, GEO2R enables the users to analyze and visualize the DEGs (Diboun et al., 2006).
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Based on the GEOquery package and Limma package of R software, GEO2R enables the users to analyze and visualize the DEGs (Diboun et al., 2006).
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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 in the article/Supplementary Material.
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In summary, through the microarray data analysis, the common functions and hub genes greatly contribute to the elucidation of the molecular pathogenesis associated with DKD.
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In summary, through the microarray data analysis, the common functions and hub genes greatly contribute to the elucidation of the molecular pathogenesis associated with DKD.
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In summary, through the microarray data analysis, the common functions and hub genes greatly contribute to the elucidation of the molecular pathogenesis associated with DKD.
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In silico nano-dissection: defining cell type specificity at transcriptional level in human disease (tubulointerstitium)
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2026-11-01T18:06:44Z
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e pathogenesis of diabetic kidney disease by microarray data analysis.
[1]
isms underlying the pathogenesis of DKD. The microarray datasets of GSE30528 and GSE30529 were downl
[2]
CD2 were identified. In summary, through the microarray data analysis, the common functions and hub
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Based on the GEOquery package and Limma package of R software, GEO2R enables the users to analyze and visualize the DEGs (Diboun et al., 2006).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36059966", "kind": "science-record", "revision": 5, "content_hash": "sha256:261e69f0212d18e0e52521180231446c907784561c4a8f09a511ec36110dcdba", "created_at": "2026-11-01T18:15:15Z", "updated_at": "2026-11-01T22:49:59Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Exploring the pathogenesis of diabetic kidney disease by microarray data analysis.", "doi": "10.3389/fphar.2022.932205", "pmid": "36059966", "authors": ["Haiyan Cao", "Xiaosheng Rao", "Junya Jia", "Tiekun Yan", "Dong Li"], "journal": "Frontiers in pharmacology", "year": 2022, "abstract": "Diabetic kidney disease (DKD) is a major complication of diabetes mellitus, and the leading contributor of end-stage renal disease. Hence, insights into the molecular pathogenesis of DKD are urgently needed. The purpose of this article is to reveal the molecular mechanisms underlying the pathogenesis of DKD. The microarray datasets of GSE30528 and GSE30529 were downloaded from the NCBI Gene Expression Omnibus (GEO) database to identify the common differentially expressed genes (DEGs) between the glomerular DKD (GDKD) and tubular DKD (TDKD), respectively. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were performed to analyze the function and pathways of the common DEGs. After constructing the protein-protein interaction (PPI) network and subnetwork analysis, three types of analyses were performed, namely, identification of hub genes, analysis of the coexpressed network, and exploration of transcription factors (TFs). Totally, 348 and 463 DEGs were identified in GDKD and TDKD, respectively. Then, 66 common DEGs (63 upregulated DEGs and three downregulated DEGs) were obtained in DKD patients. GO and KEGG pathway analyses revealed the importance of inflammation response, immune-related pathways, and extracellular matrix-related pathways, especially chemokines and cytokines, in DKD. Fifteen hub genes from the 66 common DEGs, namely, IL10RA, IRF8, LY86, C1QA, C1QB, CD53, CD1C, CTSS, CCR2, CD163, CCL5, CD48, RNASE6, CD52, and CD2 were identified. 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