Asadzadeh Azizeh, Moattar Fatemeh Shams, Moshfegh Azam
Department of Biology, Faculty of Science, Nour Danesh Institute of Higher Education, Meymeh, Isfahan, Iran.
Department of Microbiology, Faculty of Basic Sciences, Lahijan Branch, Islamic Azad University, Lahijan, Iran.
Dent Res J (Isfahan). 2025 Jan 24;22:3. doi: 10.4103/drj.drj_288_24. eCollection 2025.
Peri-implantitis is implant-associated inflammation that leads to irreversible loss of surrounding bone. Early diagnosis increases the success of peri-implantitis treatment. Despite various studies associated with this most common complication, early detection of the onset of peri-implantitis remains a major challenge. Molecular biomarkers are applicable detectors for the early detection of numerous diseases and monitoring their development. The present study aimed to predict interactome networks of up/down regulated proteins and analyze drug-gene interaction in peri-implantitis to identify the diagnostic and druggable genes.
In this study, a suitable gene expression profile related to peri-implantitis was retrieved from Gene Expression Omnibus. Screening differentially expressed genes (DEGs) was carried out based on the cut-off criteria |log2 (fold change)|>2 and < 0.05. Interactome networks were constructed and analyzed by the STRING database (Version: 12.0) and the Cytoscape software (version: 3.9.1). Finally, to investigate drug-gene interaction, detected hub genes were analyzed by DGIdb (version: 5.0.6).
A total of 216 genes were identified as DEGs (129 down-regulated and 87 up-regulated genes) in peri-implantitis. Regarding Cytoscape analysis, FCGR3B, CSF3R, AQP9, TREM1, and P2RY13 were the top 5 hub nodes of up-regulated DEGs, and CXCL10, OASL, IFIT1, RSAD2, and ISG15 were the top 5 hub nodes of down-regulated DEGs. Among these key nods, AQP9, CSF3R, CXCL10, IFIT1, ISG15, OASL, and, FCGR3B were therapeutic targets and had approved drugs.
In this research, seven genes have been identified as druggable genes in peri-implantitis which can be used to treat and diagnose this disease. However, these results and identified genes need to be validated by clinical or experimental methods.
种植体周围炎是一种与种植体相关的炎症,会导致周围骨组织不可逆的丧失。早期诊断可提高种植体周围炎治疗的成功率。尽管有各种关于这种最常见并发症的研究,但种植体周围炎发病的早期检测仍然是一项重大挑战。分子生物标志物是用于多种疾病早期检测和监测其发展的适用检测手段。本研究旨在预测上调/下调蛋白的相互作用组网络,并分析种植体周围炎中的药物-基因相互作用,以确定诊断和可药物治疗的基因。
在本研究中,从基因表达综合数据库中检索了与种植体周围炎相关的合适基因表达谱。基于|log2(倍数变化)|>2且<0.05的截断标准进行差异表达基因(DEG)的筛选。通过STRING数据库(版本:12.0)和Cytoscape软件(版本:3.9.1)构建并分析相互作用组网络。最后,为研究药物-基因相互作用,通过DGIdb(版本:5.0.6)分析检测到的枢纽基因。
在种植体周围炎中总共鉴定出216个差异表达基因(129个下调基因和87个上调基因)。关于Cytoscape分析,FCGR3B、CSF3R、AQP九、TREM1和P2RY13是上调差异表达基因的前5个枢纽节点,而CXCL10、OASL、IFIT1、RSAD2和ISG15是下调差异表达基因的前5个枢纽节点。在这些关键节点中,AQP9、CSF3R、CXCL10、IFIT1、ISG15、OASL和FCGR3B是治疗靶点且有获批药物。
在本研究中,七个基因已被鉴定为种植体周围炎中的可药物治疗基因,可用于治疗和诊断该疾病。然而,这些结果和鉴定出的基因需要通过临床或实验方法进行验证。