首页|基于网络药理学和分子对接技术对三物黄芩汤治疗肝癌的机制分析及实验观察

基于网络药理学和分子对接技术对三物黄芩汤治疗肝癌的机制分析及实验观察

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目的 通过网络药理学和分子对接技术分析三物黄芩汤治疗肝癌的潜在作用机制,并通过动物实验进行初步验证。方法 运用TCMSP数据库筛选三物黄芩汤的有效化合物,运用Drug bank、Pharm mapper、Uniport、PubMed等数据库获得三物黄芩汤的作用靶点,运用Gene cards和TCGA数据库获得肝细胞癌相关靶点,与上述三物黄芩汤作用靶点取交集后得到"药物-疾病"靶点,运用String数据库构建蛋白相互作用网络,运用David和KEGG数据库进行GO、KEGG富集分析,运用Cytoscape软件构建相应网络。运用Discovery studios软件进行分子对接,对上述网络药理学结果进行验证。采用C57小鼠肝脏原位荷瘤模型,观察三物黄芩汤干预对肝癌细胞增殖、转移的影响,并观察肝癌细胞IL-6 分子表达的变化。结果 三物黄芩汤有效成分 81个,核心成分 10个,作用靶点 249个,肝癌样本与正常样本差异靶点1420个,两者交集59个。蛋白相互作用网络频数分析显示,三物黄芩汤治疗肝细胞癌的机制与ESR1、MYC、JUN、IL-6、MMP9、EGF等靶点有关。GO和KEGG富集分析表明以IL-6为核心的IL-17 signaling pathway、TNF signaling pathway、Toll-like receptor signaling pathway等多条信号通路可能发挥重要作用。分子对接结果显示,药效分子Acacetin、Wogonin、Baicalein、Oroxylin a、Beta-sitosterol、8-Isopentenyl-kaempferol、Formononetin、Luteolin、Quercetin、Stigmasterol可与IL-6蛋白结合,进一步证实了上述结果。动物实验表明,三物黄芩汤可抑制肝种植瘤的大小和肺部转移,癌细胞IL-6含量降低,初步验证了三物黄芩汤的抗肝癌作用和机制。结论 本研究通过网络药理学和分子对接技术发现IL-6是三物黄芩汤治疗肝癌的关键靶点,进一步通过动物实验表明三物黄芩汤可降低肝癌组织IL-6表达量发挥治疗肝癌作用,为三物黄芩汤的抗肝癌应用提供理论依据。
A Network Pharmacology-and Molecular Docking-Based Analysis of the Anti-Hepatoma Mechanisms of Sanwu Huangqin Decoction with Experimental Validation
Objective Exploring the mechanisms of Sanwu Huangqin Decoction in the treatment of liver tumors based on network pharmacology and molecular docking technologies and experimental observations.Methods TCMSP database was used to screen the effective compounds contained in Sanwu Huangqin decoction,Drug bank,Pharm mapper,Uniport,PubMed and other databases were used to obtain the action targets of Sanwu Huangqin decoction,gene cards and TCGA databases were used to obtain the related targets of hepatocellular carcinoma,and the"drug-disease"target genes were obtained after the intersection with the action targets of Sanwu Huangqin decoction,and the protein interaction network was constructed using string database,David and KEGG databases were used for go and KEGG enrichment analysis,Cytoscape software was used to build the corresponding network,and discovery studios software was used for molecular docking to verify the above network pharmacology related results.The effects of Sanwu Huangqin decoction on the proliferation,the metastasis and the expression of IL-6 of cancer cells were observed.Results 81 effective components and 10 key components of Sanwu Huangqin decoction,249 targets,1420 differential targets between tumor samples and normal samples were obtained,and 59 overlapping targets were obtained.Frequency analysis of protein interaction network:the potential mechanism of Sanwu Huangqin Decoction in treating hepatocellular carcinoma is related to ESR1,Myc,Jun,IL-6,MMP9,EGF,etc.Through GO and KEGG enrichment analysis,IL-17 signaling pathway,TNF signaling pathway,Toll like receptor signaling pathway may play important roles.The results of molecular docking showed that acacetin,wogonin,baicalein,oroxylin a,beta sitosterol,8-isoopenenyl-kaempferol,formononetin,luteolin,quercetin,and stigmastrol bound to IL-6 protein,which further confirmed the above results.Animal experiments showed that Sanwu Huangqin decoction could inhibit the tumor size and the pulmonary metastasis,and the content of IL-6 in cancer cells was decreased,which preliminarily verified the anti-tumor effects and mechanism of Sanwu Huangqin decoction.Conclusion In this study,we found that IL-6 was the key target of Sanwu Huangqin decoction by network pharmacology and molecular docking technology.Sanwu Huangqin decoction could reduce the content of IL-6 in tumor tissues to inhibit liver cancer in vivo.These results provided a theoretical basis for the application of Sanwu Huangqin decoction in the treatment of liver cancer.

Sanwu Huangqin DecoctionHepatocellular carcinomaNetwork pharmacologyVirtual dockingIL-6

王华真、何磊、孟祥宇、谢圆魁

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驻马店市第二人民医院 驻马店 463000

三物黄芩汤 肝癌 网络药理学 分子对接 IL-6

驻马店市第二人民医院院内项目

2021-ZMDSPH-002

2024

世界科学技术-中医药现代化
中科院科技政策与管理科学研究所,中国高技术产业发展促进会

世界科学技术-中医药现代化

CSTPCD北大核心
影响因子:1.175
ISSN:1674-3849
年,卷(期):2024.26(3)
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