Prediction of co-expression genes and integrative analysis of gene microarray and proteomics profile of Keshan diseaseVisa övriga samt affilieringar
2018 (Engelska)Ingår i: Scientific Reports, E-ISSN 2045-2322, Vol. 8, artikel-id 231
Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
Keshan disease (KD) is a kind of endemic cardiomyopathy which has a high mortality. However, molecular mechanism in the pathogenesis of KD remains poorly understood. Serum samples were collected from 112 KD patients and 112 normal controls. Gene microarray was used to screen differently expressed genes. Genevestigator was applied to forecast co-expression genes of significant gene. iTRAQ proteomics analysis was used to verify significant genes and their co-expression genes. GO, COG, IPA and STRING were applied to undertake function categorization, pathway and network analysis separately. We identified 32 differentially expressed genes; IDH2, FEM1A, SSPB1 and their respective 30 co-expression genes; 68 differential proteins in KD. Significant proteins were categorized into 23 biological processes, 16 molecular functions, 16 cellular components, 15 function classes, 13 KD pathways and 1 network. IDH2, FEM1A, SSBP1, CALR, NDUFS2, IDH3A, GAPDH, TCA Cycle II (Eukaryotic) pathway and NADP repair pathway may play important roles in the pathogenesis of KD.
Ort, förlag, år, upplaga, sidor
London: Nature Publishing Group, 2018. Vol. 8, artikel-id 231
Nyckelord [en]
Keshan disease, cardiomyopathy, protoemics, gene array, integrative analysis
Nationell ämneskategori
Kardiologi Cell- och molekylärbiologi
Forskningsämne
kardiologi; molekylärbiologi
Identifikatorer
URN: urn:nbn:se:umu:diva-143903DOI: 10.1038/s41598-017-18599-xISI: 000419668400005PubMedID: 29321553Scopus ID: 2-s2.0-85040316779OAI: oai:DiVA.org:umu-143903DiVA, id: diva2:1173772
2018-01-142018-01-142023-03-23Bibliografiskt granskad