首页|四逆散防治胃癌前病变的网络药理学研究

四逆散防治胃癌前病变的网络药理学研究

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目的:通过网络药理学深入了解《伤寒论》经方四逆散治疗胃癌前病变(PLGC)的物质基础及其可能机制.方法:使用中药系统药理分析平台(TCMSP)数据库搜寻和筛选四逆散中药物的有效活性成分及其对应的靶点,并结合GeneCard和OMIM数据库,探索与PLGC相关的靶点.运用EXCEL软件取两者共有靶点,再运用Cytoscape软件绘制"四逆散活性成分-交集靶点-胃癌前病变"网络图;使用String平台获取蛋白质相互作用的网络图,并同时运用Cytoscape软件筛选出核心靶点并具现化为"四逆散治疗PLGC的关键靶点"网络图;利用David平台对所获靶点进行基因本体论(GO)功能和京都基因与基因组百科全书(KEGG)富集分析.结果:预测出四逆散中治疗PLGC的活性成分有 118 种,其对应 808 个靶点,疾病靶点有 2362 个,四逆散与PLGC交集靶点共有 298 个.从PPI核心网络利用 BC、CC、DC的中位值筛选出了 53 个关键靶点,进一步进行GO功能富集、KEGG通路富集分析.GO功能富集获得 1062 个生物过程,主要和细胞生长增殖、凋亡转化、以及基因转录调控生物过程密切相关.KEGG富集通路 298 条,筛选出前 20 条显示其在癌症通路、表皮生长因子信号通路、CKAP4 信号通路、胃泌素信号通路等有明显富集.结论:四逆散治疗PLGC可能是通过毛蕊异黄酮、柚皮素、华良姜素等黄酮类化合物调节癌症通路、表皮生长因子信号通路、CKAP4 信号通路、胃泌素信号通路等,发挥改善胃部微环境、减轻黏膜炎症损伤、抑制细胞的恶性生长等作用以治疗PLCG.为临床运用经方治疗PLGC提供一定的参考依据.
Network Pharmacology Study on the Prevention and Treatment of Gastric Cancer Precancerous Lesions by Si Ni San
Objective:To gain a deeper understanding of the material basis and possible mechanism of the treatment of gastric precancerous lesions(PLGC)with Sinisan,a prescription in Treatise on Febrile Diseases,through network pharmacology.Methods:The effective active ingredients and their corresponding targets in Sinisan were searched and screened using the Traditional Chinese Medicine System Pharmacology Analysis Platform(TCMSP)database,and the targets related to PLGC were explored by combining GeneCard and OMIM databases.EXCEL software was used to ob-tain the common targets of the two,and then Cytoscape software was used to draw a network diagram of"Sinisan active ingredients-intersection targets-gastric precancerous lesions";the String platform was used to obtain the network diagram of protein interactions,and the Cytoscape software was used to screen out the core targets and visualize them into a network diagram of"Sinisan key targets for the treatment of PLGC";David platform was used to perform gene ontology(GO)function and Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analysis on the obtained targets.Results:It was predicted that there were 118 active ingredients in Sini San for the treatment of PLGC,cor-responding to 808 targets,2362 disease targets,and 298 targets intersecting Sini San and PLGC.53 key targets were screened out from the PPI core network using the median values of BC,CC,and DC,and further GO functional enrich-ment and KEGG pathway enrichment analysis were performed.GO functional enrichment obtained 1062 biological processes,which were mainly closely related to cell growth and proliferation,apoptosis transformation,and gene tran-scription regulation biological processes.There were 298 KEGG enriched pathways,and the top 20 were screened out,showing that they were significantly enriched in cancer pathways,epidermal growth factor signaling pathways,CKAP4 signaling pathways,gastrin signaling pathways,etc.Conclusion:Sinisan can treat PLGC by regulating cancer pathways,epidermal growth factor signaling pathways,CKAP4 signaling pathways,gastrin signaling pathways,etc.through flavo-noids such as calycosin,naringenin,and galangin,thereby improving gastric microenvironment,reducing mucosal in-flammatory damage,and inhibiting the malignant growth of cells to treat PLGC.This provides a certain reference for the clinical application of traditional Chinese medicine prescriptions to treat PLGC.

Network pharmacologySinisangastric precancerous lesionsenrichment analysis

彭楚杰、阳国彬、邹莹

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湖北中医药大学 湖北 武汉 430065

湖北省襄阳市中医医院,襄阳市中医药研究所 湖北 襄阳 441000

网络药理学 四逆散 胃癌前病变 富集分析

2024

中医药临床杂志
中华中医药学会

中医药临床杂志

影响因子:0.636
ISSN:1672-7134
年,卷(期):2024.36(11)