首页|基于网络药理学及分子对接研究黄芪-党参治疗胃癌的分子生物学机制

基于网络药理学及分子对接研究黄芪-党参治疗胃癌的分子生物学机制

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目的 采用网络药理学及分子对接研究黄芪-党参有效成分治疗胃癌的分子生物学机制。方法 采用中药系统药理学数据库与分析平台检索并收集黄芪与党参的活性成分及其对应靶点。通过人类孟德尔遗传数据库和人类基因组注释数据库收集与胃癌相关靶点,并与药物成分所对应的靶点相比较,筛选出相同部分,即获得黄芪-党参与胃癌重合的潜在靶点。采用可视化Cytoscape3。9。0软件建立对药物与疾病靶点相映射得到黄芪-党参治疗胃癌的作用靶点,运用STRING软件构建"化合物-靶点"作用网络与蛋白质相互作用网络,筛选发挥治疗作用的关键成分与关键靶点,对关键靶点进行基因本体和京都基因与基因组百科全书富集分析获知其潜在的作用机制。结果 共筛选出黄芪-党参63个候选活性成分,主要发挥抗胃癌的活性成分有木犀草素、槲皮素、山柰酚、异鼠李素等6个,主要作用靶点有CCND1、MYC、TP53、FOS、MCL1、CDK4、RUNX2等13个。主要集中于有丝分裂细胞周期的调控、DNA转录的激活、多种肽酶活性等生物学过程,以及磷酸肌醇-3激酶/蛋白激酶B信号通路、P53信号通路等生物学通路。分子对接结果表明药物有效成分与对应靶点均具有较强的结合活性。结论 黄芪-党参有效活性成分通过调控细胞凋亡、介导磷酸肌醇-3激酶/蛋白激酶B等信号通路抑制胃癌细胞增殖,促进癌细胞凋亡发挥抗胃癌作用,具有多成分、多靶点、多通路的作用机制。
Study on molecular biological mechanism of Astragalus membranaceus-Codonopsis pilosula in the treatment of gastric cancer based on network pharmacology and molecular docking
Objective To study the molecular biology mechanism of the effective ingredients of Astrag-alus membranaceus-Codonopsis pilosula in the treatment of gastric cancer by network pharmacology and mo-lecular docking.Methods The active ingredients and corresponding targets of Astragalus membranaceus-Codonopsis pilosula were collected from the database of Traditional Chinese Medicine Systems Pharmacology.The targets related to gastric cancer were collected from the Online Mendelian Inheritance in Man and Gene-Cards databases,and the same parts were screened out by comparing with the corresponding targets of drug components,that is,potential targets for overlapping Astragalus membranaceus-Codonopsis pilosula and gas-tric cancer were obtained.The visual Cytoscape3.9.0 software was used to establish the mapping between drugs and disease targets to obtain the action targets of Astragalus membranaceus-Codonopsis pilosula in the treatment of gastric cancer.The STRING software was used to construct the"compound target"action net-work and protein interaction network to screen the key components and key targets that played a role in the treatment of gastric cancer.Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analy-sis were used to analyze the potential mechanisms of key targets.Results A total of 63 candidate active ingre-dients of Astragalus membranaceus-Codonopsis pilosula were screened out,and six active ingredients were mainly luteolin,quercetin,kaempferol and isorhamnetin,and 13 main targets were CCND1,MYC,TP53,FOS,MCL1,CDK4 and RUNX2.It mainly focused on biological processes such as the regulation of the mitotic cell cycle,the activation of DNA transcription,and multiple peptidase activities,and mainly focuses on the biologi-cal pathways such as phosphatidylinositol 3 kinase/protein kinase B signaling pathway and P53 signaling path-way.Molecular docking results showed that the active compounds of the drugs had strong binding activity with their corresponding targets.Conclusion The active components of Astragalus membranaceus-Codonop-sis pilosula inhibit the proliferation of gastric cancer cells and promote the apoptosis of cancer cells by regula-ting cell apoptosis and mediating phosphatidylinositol 3 kinase/protein kinase B signaling pathway,which has a multi-component,multi-target and multi-pathway mechanism.

Gastric tumorAstragalus membranaceusCodonopsis pilosulaNetwork pharmacologyMolecular docking

罗春苗、覃敏珍、鲍美霜、姚敦卫、朱博杰、凌春丰

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百色市人民医院消化内科二区,广西百色 533000

百色市人民医院中医科,广西百色 533000

胃肿瘤 黄芪 党参 网络药理学 分子对接

广西壮族自治区卫生健康委员会自筹经费科研课题

Z20211090

2024

现代医药卫生
重庆市卫生信息中心

现代医药卫生

影响因子:0.758
ISSN:1009-5519
年,卷(期):2024.40(4)
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