Zhu Xianyang, Guo Wen
Department of Orthopedics, Taizhou People's Hospital, Taizhou, China.
Public Health Genomics. 2021;24(5-6):267-279. doi: 10.1159/000517308. Epub 2021 Aug 2.
This study aimed to screen and validate the crucial genes involved in osteoarthritis (OA) and explore its potential molecular mechanisms.
Four expression profile datasets related to OA were downloaded from the Gene Expression Omnibus (GEO). The differentially expressed genes (DEGs) from 4 microarray patterns were identified by the meta-analysis method. The weighted gene co-expression network analysis (WGCNA) method was used to investigate stable modules most related to OA. In addition, a protein-protein interaction (PPI) network was built to explore hub genes in OA. Moreover, OA-related genes and pathways were retrieved from Comparative Toxicogenomics Database (CTD).
A total of 1,136 DEGs were identified from 4 datasets. Based on these DEGs, WGCNA further explored 370 genes included in the 3 OA-related stable modules. A total of 10 hub genes were identified in the PPI network, including AKT1, CDC42, HLA-DQA2, TUBB, TWISTNB, GSK3B, FZD2, KLC1, GUSB, and RHOG. Besides, 5 pathways including "Lysosome," "Pathways in cancer," "Wnt signaling pathway," "ECM-receptor interaction" and "Focal adhesion" in CTD and enrichment analysis and 5 OA-related hub genes (including GSK3B, CDC42, AKT1, FZD2, and GUSB) were identified.
In this study, the meta-analysis was used to screen the central genes associated with OA in a variety of gene expression profiles. Three OA-related modules (green, turquoise, and yellow) containing 370 genes were identified through WGCNA. It was discovered through the gene-pathway network that GSK3B, CDC42, AKT1, FZD2, and GUSB may be key genes related to the progress of OA and may become promising therapeutic targets.
本研究旨在筛选和验证骨关节炎(OA)相关的关键基因,并探索其潜在的分子机制。
从基因表达综合数据库(GEO)下载了4个与OA相关的表达谱数据集。通过荟萃分析方法鉴定了来自4种微阵列模式的差异表达基因(DEG)。采用加权基因共表达网络分析(WGCNA)方法研究与OA最相关的稳定模块。此外,构建了蛋白质-蛋白质相互作用(PPI)网络以探索OA中的枢纽基因。此外,还从比较毒理基因组学数据库(CTD)中检索了OA相关基因和通路。
从4个数据集中共鉴定出1136个DEG。基于这些DEG,WGCNA进一步探索了3个与OA相关的稳定模块中包含的370个基因。在PPI网络中总共鉴定出10个枢纽基因,包括AKT1、CDC42、HLA-DQA2、TUBB、TWISTNB、GSK3B、FZD2、KLC1、GUSB和RHOG。此外,在CTD中鉴定出5条通路,包括“溶酶体”、“癌症通路”、“Wnt信号通路”、“细胞外基质-受体相互作用”和“粘着斑”,并进行了富集分析,以及5个与OA相关的枢纽基因(包括GSK3B、CDC42、AKT1、FZD2和GUSB)。
在本研究中,荟萃分析用于在各种基因表达谱中筛选与OA相关的核心基因。通过WGCNA鉴定出3个与OA相关的模块(绿色、蓝绿色和黄色),包含370个基因。通过基因-通路网络发现,GSK3B、CDC42、AKT1,、FZD2和GUSB可能是与OA进展相关的关键基因,可能成为有前景的治疗靶点。