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使用生物信息学分析鉴定骨关节炎滑膜炎相关的通路和基因。

Identification of pathways and genes associated with synovitis in osteoarthritis using bioinformatics analyses.

机构信息

Department of Orthopaedic Surgery, Jinling Hospital(Nanjing General Hospital of Nanjing Military Region), The First School of Clinical Medicine, Southern Medical University(Guangzhou), 305 East Zhongshan Road, Nanjing, 210002, Jiangsu Province, China.

Department of Orthopaedic Surgery, Hainan Provincial People's Hospital, Haikou, 570311, Hainan Province, China.

出版信息

Sci Rep. 2018 Jul 3;8(1):10050. doi: 10.1038/s41598-018-28280-6.

Abstract

Synovitis in osteoarthritis (OA) is a very common condition. However, its underlying mechanism is still not well understood. This study aimed to explore the molecular mechanisms of synovitis in OA. The gene expression profile GSE82107 (downloaded from the Gene Expression Omnibus database) included 10 synovial tissues of the OA patients and 7 synovial tissues of healthy people. Subsequently, differentially expressed gene (DEG) analysis, GO (gene ontology) enrichment analysis, pathway analysis, pathway network analysis, and gene signal network analysis were performed using Gene-Cloud of Biotechnology Information (GCBI). A total of 1,941 DEGs consisting of 1,471 upregulated genes and 470 downregulated genes were determined. Genes such as PSMG3, LRP12 MIA-RAB4B, ETHE1, SFXN1, DAZAP1, RABEP2, and C9orf16 were significantly regulated in synovitis of OA. In particular, the MAPK signalling pathway, apoptosis, and pathways in cancer played the most important roles in the pathway network. The relationships between these pathways were also analysed. Genes such as NRAS, SPHK2, FOS, CXCR4, PLD1, GNAI2, and PLA2G4F were strongly implicated in synovitis of OA. In summary, this study indicated that several molecular mechanisms were implicated in the development and progression of synovitis in OA, thus improving our understanding of OA and offering molecular targets for future therapeutic advances.

摘要

骨关节炎(OA)中的滑膜炎是一种非常常见的病症。然而,其潜在的机制仍未被很好地理解。本研究旨在探索 OA 中滑膜炎的分子机制。基因表达谱 GSE82107(从基因表达综合数据库中下载)包括 10 例 OA 患者的滑膜组织和 7 例健康人的滑膜组织。随后,使用生物技术信息基因云(GCBI)进行差异表达基因(DEG)分析、GO(基因本体论)富集分析、通路分析、通路网络分析和基因信号网络分析。确定了 1941 个差异表达基因,其中包括 1471 个上调基因和 470 个下调基因。PSMG3、LRP12、MIA-RAB4B、ETHE1、SFXN1、DAZAP1、RABEP2 和 C9orf16 等基因在 OA 滑膜炎中受到显著调节。特别是 MAPK 信号通路、细胞凋亡和癌症通路在通路网络中起着最重要的作用。还分析了这些通路之间的关系。NRAS、SPHK2、FOS、CXCR4、PLD1、GNAI2 和 PLA2G4F 等基因强烈参与 OA 滑膜炎。总之,本研究表明,几个分子机制参与了 OA 中滑膜炎的发展和进展,从而提高了我们对 OA 的认识,并为未来的治疗进展提供了分子靶点。

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