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• W3097365903 abstract "Coronary heart disease (CHD) is common in patients with diabetes mellitus (DM), however, the relevant mechanism remains elusive. The whole blood gene expression profiles of healthy control, patients with DM, patients with DM and CHD (DMCHD) were used to performed weight gene correlation network analysis (WGCNA) to identify the gene modules associated with the progress from DM to DMCHD. The candidate module was significantly involved in immune- and T cell activity-related biological process. GSEA results suggested that lysosome and apoptosis were enriched in DM and DMCHD samples. The protein-protein-KEGG pathway network may reveal the potential transcriptional regulatory network involving in DM-related atherosclerosis. Nineteen genes (RTKN, DCP1B, PDZD4, CACNA2D2, TSEN54, PVRIG, PLEKHF1, NKG7, ZAP70, NUDCD3, SLAMF6, CCDC107, NAG6, ZDHHC14, EOMES, VIL2, WDR54, DMAP1and PMPCA) were considered as DM-related atherogenesis genes (DRAGs). The Gene Set Variation Analysis (GSVA) score of the DRAG set was increased in the progress from DM to DMCHD. ROC curve analysis showed that ZAP70, TSEN54 and PLEKHF1 may be potential blood circulation biomarkers for DMCHD in patients with DM. In conclusion, we identified nineteen hallmark genes involving in diabetes mellitus-related atherogenesis and constructed a potential transcriptional regulatory network involving in DM-related atherosclerosis." @default.
• W3097365903 created "2020-11-09" @default.
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• W3097365903 date "2020-10-28" @default.
• W3097365903 modified "2023-10-18" @default.
• W3097365903 title "Comprehensive Identification of Key Genes Involved in Development of Diabetes Mellitus-Related Atherogenesis Using Weighted Gene Correlation Network Analysis" @default.
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• W3097365903 doi "https://doi.org/10.3389/fcvm.2020.580573" @default.
• W3097365903 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7655645" @default.
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