Discovery of Key Genes in Dermatomyositis Based on the Gene Expression Omnibus Database

被引:7
|
作者
Xie, Shuoshan [1 ]
Luo, Hui [1 ]
Zhang, Huali [2 ]
Zhu, Honglin [1 ]
Zuo, Xiaoxia [1 ]
Liu, Sijia [1 ]
机构
[1] Cent S Univ, Dept Rheumatol, Xiangya Hosp, Changsha 410000, Hunan, Peoples R China
[2] Cent S Univ, Dept Pathophysiol, Xiangya Sch Med, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
dermatomyositis; microarray; bioinformatics; human skeletal muscle cell; INTERFERON-INDUCIBLE GENE; RIG-I; INFLAMMATORY MYOPATHIES; DISEASE-ACTIVITY; POLYMYOSITIS; BLOOD; PROTEIN; CANCER; CELLS; RNA;
D O I
10.1089/dna.2018.4256
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to identify biomarkers of dermatomyositis (DM). The analysis was conducted by retrieving DM-related cDNA microarray data sets from public databases. Gene ontology, Kyoto encyclopedia of genes and genomes, and protein-protein interaction analyses were performed, together with quantitative PCR-based detection of biomarkers in muscle tissue after stimulation with serum from patients with DM or healthy controls. Our analysis of five microarray data sets identified 20 common differentially expressed genes that are closely associated with DM. PCR analysis showed that mRNAs of IFITM2, LY6E, DDX58, and IFI6 were expressed at significantly higher levels in the muscle tissue of patients with DM than in normal muscle tissues. These mRNAs were also upregulated in human skeletal muscle cells stimulated with the serum from patients with DM. The results of integrated analyses of the DM microarray data and the mRNA levels of genes showed significant differences between the muscle tissues of DM patients and controls, which could indicate key pathogenic genes and novel therapeutic targets for DM.
引用
收藏
页码:982 / 992
页数:11
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