Department of Orthopedic, The Second Affiliated Hospital, Zhejiang University School of Medicine, #88 Jiefang Road, Hangzhou City, 310001, Zhejiang Province, People's Republic of China.
Key Laboratory of Motor System Disease Research and Precision Therapy of Zhejiang Province, Hangzhou City, Zhejiang Province, China.
Sci Rep. 2023 Jul 24;13(1):11972. doi: 10.1038/s41598-023-39258-4.
Osteonecrosis of the femoral head (ONFH) is a multifactorial disease leading to severely limited function. By far, the etiology and pathogenesis of ONFH are not fully understood, and surgery is the only effective way to treat ONFH. This study aims to identify hub genes and therapeutic drugs in ONFH. Two gene expression profiles were downloaded from the gene expression omnibus database, and the hub genes and candidate drugs for ONFH were identified through integrated bioinformatics analysis and cross-validated by literature mining. A total of 159 DEGs were identified. PTGS2, LRRK2, ANXA5, IGF1R, MCL1, TIMP2, LYN, CD68, CBL, and RUNX2 were validated as 10 hub genes, which has considerable implications for future genetic research and related research fields of ONFH. Our findings indicate that 85 drugs interact with ONFH, with most drugs exhibiting a positive impact on ONFH by promoting osteogenesis and angiogenesis or inhibiting microcirculation embolism, rather than being anti-inflammatory. Our study provides novel insights into the pathogenesis, prevention, and treatment of ONFH.
股骨头坏死(ONFH)是一种多因素疾病,导致严重的功能受限。到目前为止,ONFH 的病因和发病机制尚未完全阐明,手术是治疗 ONFH 的唯一有效方法。本研究旨在鉴定 ONFH 的枢纽基因和治疗药物。从基因表达综合数据库中下载了两个基因表达谱,通过综合生物信息学分析鉴定枢纽基因和 ONFH 的候选药物,并通过文献挖掘进行交叉验证。共鉴定出 159 个差异表达基因。PTGS2、LRRK2、ANXA5、IGF1R、MCL1、TIMP2、LYN、CD68、CBL 和 RUNX2 被验证为 10 个枢纽基因,这对未来的遗传研究和 ONFH 的相关研究领域具有重要意义。我们的研究结果表明,有 85 种药物与 ONFH 相互作用,大多数药物通过促进成骨和血管生成或抑制微循环栓塞对 ONFH 产生积极影响,而不是抗炎作用。本研究为 ONFH 的发病机制、预防和治疗提供了新的见解。