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pmid:31277135
Identification of miRNAs-genes regulatory network in diabetic nephropathy based on bioinformatics analysis.
Fengying Yang · Zhenhai Cui · Hongjun Deng · Ying Wang · Yang Chen · Huiqing Li · Li Yuan
Medicine · 2019 doi:10.1097/MD.0000000000016225
Paper
complete
Experiment
partial
Data
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Analysis
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Execution
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Complete file
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The aim of this study was to explore potential miRNAs-genes regulatory network and biomarkers for the pathogenesis of DN using bioinformatics methods.Gene expression profiling data related to DN (GSE1009) was obtained from the Gene Expression Omnibus (GEO) database, and then differentially expressed genes (DEGs) between DN patients and normal individuals were screened using GEO2R, followed by a series of bioinformatics analyses, including identifying key genes, conducting pathway enrichment analysis, predicting and identifying key miRNAs, and establishing regulatory relationships between key miRNAs and their target genes.A total of 600 DEGs associated with DN were identified. An additional 7 key DEGs, including 6 downregulated genes, such as vascular endothelial growth factor α (VEGFA) and COL4A5, and 1 upregulated gene (CCL19), were identified in another dataset (GSE30528) from glomeruli samples. Pathway analysis showed that the down- and upregulated DEGs were enriched in 14 and 6 pathways, respectively, with 7 key genes mainly involved in extracellular matrix-receptor interaction, PI3K/Akt signaling, focal adhesion, and Rap1 signaling. The relationships between miRNAs and target genes were constructed, showing that miR-29 targeted COL4A and VEGFA, miR-200 targeted VEGFA, miR-25 targeted ITGAV, and miR-27 targeted EGFR.MiR-29 and miR-200 may play important roles in DN. VEGFA and COL4A5 were targeted by miR-29 and VEGFA by miR-200, which may mediate multiple signaling pathways leading to the pathogenesis and development of DN.", "claims": [{"id": "claim-method", "statement": "The online analysis tool GEO2R[13] was used to preprocess and analyze the microarray data and screen for DEGs associated with DN. The screening conditions were P value <.01 and |logFC| ≥1.5. 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