Identification and Validation of Pivotal Genes in Osteoarthritis Combined with WGCNA Analysis.

IF 4.1 2区 医学 Q2 IMMUNOLOGY Journal of Inflammation Research Pub Date : 2025-01-31 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S504717
Chengzhuo Yang, Xinhua Chen, Jin Liu, Wenhao Wang, Lihua Sun, Youhong Xie, Qing Chang
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Abstract

Introduction: The prevalence of osteoarthritis (OA), the most common chronic joint condition, is increasing due to the aging population and escalating obesity rates, leading to a significant impact on human health and well-being. Thus, analyzing the key targets of OA through bioinformatics can help discover new biomarkers to improve its diagnosis.

Methods: The microarray and RNA-seq results were screened from the Gene Expression Omnibus (GEO) database. Functional enrichment analyses, protein-protein interaction (PPI) analysis, and weighted gene co-expression network analysis (WGCNA) of the DEGs were performed. RT-qPCR and WB were further performed to verify the hub gene expression in OA rat.

Results: In this study, 35 key genes were identified through differential expression analysis and weighted gene co-expression network analysis (WGCNA) using the GSE169077 and GSE114007 datasets. Enrichment analysis revealed that these key genes were predominantly enriched in the HIF-1 signaling pathway, ECM-receptor interaction, and FoxO signaling pathway. Through the integration of protein-protein interaction (PPI) analysis, validation in animal models and ROC curve analysis, four pivotal genes (GADD45B, CLDN5, HILPDA and CDKN1B) were finally identified.

Conclusion: In conclusion, these identified key genes could serve as novel targets for predicting and treating OA, offering fresh insights into its etiology and pathogenesis.

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结合WGCNA分析骨关节炎关键基因的鉴定与验证。
引言:骨关节炎(OA)是最常见的慢性关节疾病,由于人口老龄化和肥胖率的上升,其患病率正在增加,对人类健康和福祉产生了重大影响。因此,通过生物信息学分析OA的关键靶点,有助于发现新的生物标志物,提高OA的诊断水平。方法:从Gene Expression Omnibus (GEO)数据库中筛选微阵列和RNA-seq结果。对deg进行功能富集分析、蛋白-蛋白相互作用(PPI)分析和加权基因共表达网络分析(WGCNA)。进一步采用RT-qPCR和WB方法验证OA大鼠中枢基因的表达。结果:本研究使用GSE169077和GSE114007数据集,通过差异表达分析和加权基因共表达网络分析(WGCNA)鉴定出35个关键基因。富集分析显示,这些关键基因主要富集于HIF-1信号通路、ecm受体相互作用通路和FoxO信号通路。通过整合蛋白-蛋白相互作用(PPI)分析、动物模型验证和ROC曲线分析,最终鉴定出GADD45B、CLDN5、HILPDA和CDKN1B四个关键基因。结论:这些鉴定的关键基因可作为预测和治疗OA的新靶点,为OA的病因和发病机制提供新的认识。
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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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