Yi Jing-Rui, Zeng Bang, Liu Jian-Feng, Man Qi-Wen
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University, Wuhan, China.
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University, Wuhan, China.
J Stomatol Oral Maxillofac Surg. 2025 Jun;126(3):102105. doi: 10.1016/j.jormas.2024.102105. Epub 2024 Oct 2.
This study aimed to explore active ingredients in Polygonum cuspidatum with potential effects on odontogenic keratocysts (OKCs) using network pharmacological approach and bioinformatic gene analysis. The active ingredients and targets of P. cuspidatum were selected from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) database, and the ingredient-target network was constructed using Cytoscape software. Differentially expressed genes (DEGs) of OKC were selected and Gene Ontology (GO) enrichment analysis were performed through bioinformatic analysis using Gene Expression Omnibus (GEO) dataset GSE38494. The STRING database platform was used to draw protein-protein interaction network diagram, then the hub gene analysis was performed by Cytoscape software. AutoDock Vina software was used to perform molecular docking verification of the effects of the active ingredients on potential core targets. Finally, we use OKC nude animal model to testify the potential effects of P. cuspidatum. Ten active ingredients of P. cuspidatum were obtained. A total of 205 drug targets and 38 potential core targets of P. cuspidatum were confirmed in OKCs. The hub genes included PPARG, SPP1, COL3A1, MMP2, HMOX1, CCL2, CXCL10, VCAM1, RUNX2 and IRF1. Molecular docking showed that the key active ingredients including luteolin and quercetin which exhibited good docking activity with key target proteins (VCAM1, HMOX1 and MMP2). GO enrichment revealed that the pathways of P. cuspidatum acting on OKCs included the response to toxic substance, response to nutrient levels and response to xenobiotic stimulus. P. cuspidatum treatment in OKC could significantly down-regulate COL3A1 and MMP2 expressions in vivo and vitro. Our study indicated that P. cuspidatum is a potential therapeutic candidate for OKCs.
本研究旨在运用网络药理学方法和生物信息学基因分析,探索虎杖中对牙源性角化囊肿(OKCs)具有潜在作用的活性成分。虎杖的活性成分和靶点从中药系统药理学数据库与分析平台(TCMSP)数据库中选取,并使用Cytoscape软件构建成分-靶点网络。选取OKC的差异表达基因(DEGs),并通过使用基因表达综合数据库(GEO)数据集GSE38494进行生物信息学分析,进行基因本体(GO)富集分析。利用STRING数据库平台绘制蛋白质-蛋白质相互作用网络图,然后通过Cytoscape软件进行枢纽基因分析。使用AutoDock Vina软件对活性成分对潜在核心靶点的作用进行分子对接验证。最后,我们使用OKC裸鼠动物模型验证虎杖的潜在作用。获得了虎杖的10种活性成分。在OKCs中确认了虎杖总共205个药物靶点和38个潜在核心靶点。枢纽基因包括PPARG、SPP1、COL3A1、MMP2、HMOX1、CCL2、CXCL10、VCAM1、RUNX2和IRF1。分子对接表明,包括木犀草素和槲皮素在内的关键活性成分与关键靶蛋白(VCAM1、HMOX1和MMP2)表现出良好的对接活性。GO富集显示,虎杖作用于OKCs的途径包括对有毒物质的反应、对营养水平的反应和对外源生物刺激的反应。虎杖治疗OKC可在体内和体外显著下调COL3A1和MMP2的表达。我们的研究表明,虎杖是OKCs的一种潜在治疗候选药物。