دورية أكاديمية

Meta-Analysis of Polymyositis and Dermatomyositis Microarray Data Reveals Novel Genetic Biomarkers

التفاصيل البيبلوغرافية
العنوان: Meta-Analysis of Polymyositis and Dermatomyositis Microarray Data Reveals Novel Genetic Biomarkers
المؤلفون: Jaeseung Song, Daeun Kim, Juyeon Hong, Go Woon Kim, Junghyun Jung, Sejin Park, Hee Jung Park, Jong Wha J. Joo, Wonhee Jang
المصدر: Genes, Vol 10, Iss 11, p 864 (2019)
بيانات النشر: MDPI AG, 2019.
سنة النشر: 2019
المجموعة: LCC:Genetics
مصطلحات موضوعية: polymyositis, dermatomyositis, meta-analysis, multiple-phenotype analysis, Genetics, QH426-470
الوصف: Polymyositis (PM) and dermatomyositis (DM) are both classified as idiopathic inflammatory myopathies. They share a few common characteristics such as inflammation and muscle weakness. Previous studies have indicated that these diseases present aspects of an auto-immune disorder; however, their exact pathogenesis is still unclear. In this study, three gene expression datasets (PM: 7, DM: 50, Control: 13) available in public databases were used to conduct meta-analysis. We then conducted expression quantitative trait loci analysis to detect the variant sites that may contribute to the pathogenesis of PM and DM. Six-hundred differentially expressed genes were identified in the meta-analysis (false discovery rate (FDR) < 0.01), among which 317 genes were up-regulated and 283 were down-regulated in the disease group compared with those in the healthy control group. The up-regulated genes were significantly enriched in interferon-signaling pathways in protein secretion, and/or in unfolded-protein response. We detected 10 single nucleotide polymorphisms (SNPs) which could potentially play key roles in driving the PM and DM. Along with previously reported genes, we identified 4 novel genes and 10 SNP-variant regions which could be used as candidates for potential drug targets or biomarkers for PM and DM.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2073-4425
80108644
Relation: https://www.mdpi.com/2073-4425/10/11/864; https://doaj.org/toc/2073-4425
DOI: 10.3390/genes10110864
URL الوصول: https://doaj.org/article/41956d801086449c99386a3b9253848e
رقم الأكسشن: edsdoj.41956d801086449c99386a3b9253848e
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20734425
80108644
DOI:10.3390/genes10110864