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骨关节炎滑膜与软骨相比独特的基因表达谱:对公开可获取的微阵列数据集的分析。

Unique gene expression profile in osteoarthritis synovium compared with cartilage: analysis of publicly accessible microarray datasets.

作者信息

Park Robin, Ji Jong Dae

机构信息

Division of Rheumatology, College of Medicine, Korea University, 126-1, Anam-Dong 5-Ga, Sungbuk-Ku, Seoul, 136-705, South Korea.

出版信息

Rheumatol Int. 2016 Jun;36(6):819-27. doi: 10.1007/s00296-016-3451-1. Epub 2016 Mar 4.

Abstract

The purpose of this study was to identify a gene expression signature in osteoarthritis (OA) synovium and genomic pathways likely to be involved in the pathogenesis of OA. Four publicly accessible microarray studies from synovium of OA patients were integrated, and a transcriptomic and network-based meta-analysis was performed. Based on pathways according to the Kyoto Encyclopedia of Genes and Genomes, functional enrichment analysis was performed. Meta-analysis results of OA synovium were compared to two previously published studies of OA cartilage to determine the relative number of common and specific DEGs of the cartilage and synovium. According to our meta-analysis, a total of 1350 genes were found to be differentially expressed in the synovium of OA patients as compared to that of healthy controls. Pathway analysis found 41 significant pathways in the total DEGs, and 22 and 16 pathways in the upregulated and downregulated DEGs, respectively. Cell adhesion molecules and cytokine-cytokine receptor interaction were the most significant pathway in the upregulated and downregulated DEGs, respectively. Comparison of meta-analysis results of OA synovium with results of two previous studies of OA cartilage identified 85 common genes and 1632 cartilage-specific DEGs and 1265 synovium-specific DEGs in the first study; and 142 common genes, and 856 cartilage-specific DEGs and 1208 synovium-specific DEGs in the second study. Our results show a small overlap between the DEGs of the synovium compared to DEGs of the cartilage, suggesting different pathogenic mechanisms that are specific to the synovium.

摘要

本研究的目的是确定骨关节炎(OA)滑膜中的基因表达特征以及可能参与OA发病机制的基因组途径。整合了四项来自OA患者滑膜的公开可获取的微阵列研究,并进行了基于转录组和网络的荟萃分析。根据京都基因与基因组百科全书的途径进行了功能富集分析。将OA滑膜的荟萃分析结果与之前发表的两项关于OA软骨的研究进行比较,以确定软骨和滑膜中共同和特异性差异表达基因(DEG)的相对数量。根据我们的荟萃分析,与健康对照相比,共发现1350个基因在OA患者的滑膜中差异表达。通路分析在总DEG中发现了41条显著通路,上调和下调的DEG中分别有22条和16条通路。细胞粘附分子和细胞因子-细胞因子受体相互作用分别是上调和下调DEG中最显著的通路。将OA滑膜的荟萃分析结果与之前两项OA软骨研究的结果进行比较,在第一项研究中确定了85个共同基因、1632个软骨特异性DEG和1265个滑膜特异性DEG;在第二项研究中确定了142个共同基因、856个软骨特异性DEG和1208个滑膜特异性DEG。我们的结果表明,滑膜的DEG与软骨的DEG之间存在小的重叠,这表明滑膜存在特异性的不同致病机制。

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