Identification of key genes and pathways associated with dilated cardiomyopathy development by bioinformatics analysis / 西安交通大学学报(医学版)

【Objective】 To explore the potential biomarkers and related enrichment pathways of dilated cardiomyopathy （DCM） by bioinformatics methods. 【Methods】 The data sets related to DCM in GEO database were searched， and microarray data sets GSE42955 and GSE1869 of human cardiomyocytes were extracted. Then， the differentially expressed genes （DEGS） were analyzed using R language， and the protein-protein interaction network was analyzed to identify the core genes and core modules of differential expression. The gene ontology database （GO） enrichment and Kyoto Gene and Genome Encyclopedia （KEGG） pathway analyses were performed. The data sets related to DCM in ArrayExpress database were searched， and the human cardiomyocytes microarray data set E-TABM-480 was extracted to verify the expressions of core genes and modules. 【Results】 We identified 10 DEGS， namely， DZIP3， FBXO32， BTBD6， FBXL5， ASB8， COMMD1， LTN1， FBXO21， RCHY1 and ARIH2， and the core DEG was DZIP3. After GO and KEGG analyses， the GO and KEGG of the above DEGS were mainly related to the ubiquitin-proteasome system. 【Conclusion】 Bioinformatics analysis shows that the ubiquitin-proteasome system plays an important role in the pathogenesis of DCM， and the mechanism remains to be further studied.

SUPEROXIDE DISMUTASE ACTIVITY AND MEMBRANE LIPIDSCOMPOSITION OF ERYTHROCYTES IN PATIENTS WITH DILATEDCARDIOMYOPATHY / 药物分析学报

Objective To further confirm the role of lipid-peroxidation caused by oxygen free radicals injury played in the pathogenesis of dilsted cardiomypathy. Methods The superoxide dismutase activities and lipids composi tion of erythrocytes in 18 patients with dilated cardiomyopathy and 16 healthy controls were measured. Results ① Su peroxide dismutase(SOD) activites of erythrocytes were lower in dilated cardiomyopathy(DCM) patients than that in healthy controls (P ＜0. 001). ②The lipids composition of erythrocytes has changed in the DCM patients compared with healthy controls: total lipids changed little (P＞0. 05); total phospholipids were lower, but not significantly (P ＞0.05); total cholesterol increased significantly (P ＜0. 05). The cholesterol to phospholipids molecular ratio of erythrocyte membrane has increased remarkably (P＞0. 05). Conclusion It can be supposed that decreased SOD ac tivities play an important role in the damage of membrane system and the pathogensis of DCM.