The mechanism of Weiqi decoction treating gastric cancer: a work based on network pharmacology and experimental verification.

IF 2.7 3区 生物学
Xu Huang, Zhihong Pan, Lei Shen, Huan Chen, Chang Chen, Tingting Lv, Yuzhou Mei
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引用次数: 0

Abstract

Background: Weiqi Decoction (WQD) is an empirical prescription traditionally used in China for the treatment of precancerous gastric cancer (GC) lesions. This study aimed to elucidate the potential pharmacological mechanisms of WQD in GC therapy.

Methods: Active ingredients, corresponding targets, and GC-related genes were identified using public databases. A protein-protein interaction (PPI) network was constructed via the STRING database, and functional enrichment analyses were conducted using the DAVID platform. Gene expression and survival analyses were performed using the GEPIA database. Molecular docking was conducted with AutoDock Vina and visualized using PyMOL. The effects of WQD on GC cell viability, proliferation, migration, and invasion were evaluated through CCK-8, colony formation, and Transwell assays.

Results: WQD contained 43 active ingredients targeting 751 potential genes, including 458 GC-related targets. Quercetin, luteolin, and kaempferol were identified as key active compounds. PPI network analysis revealed nine core targets, including TP53 and SRC, which may mediate the anti-GC effects of WQD. GO enrichment analysis indicated involvement in 726 biological processes, 91 cellular components, and 177 molecular functions, while KEGG pathway analysis suggested modulation of the AGE-RAGE, PI3K-Akt, and HIF-1 signaling pathways. GEPIA database analysis confirmed that EP300, HSP90AA1, HSP90AB1, SRC, and TP53 were highly expressed in GC. Molecular docking demonstrated strong binding affinities between the key active compounds and core targets. In vitro experiments further validated that WQD extract inhibited GC cell viability, proliferation, migration, and invasion.

Conclusion: WQD exhibits therapeutic potential against GC by regulating multiple targets and signaling pathways. These findings provide mechanistic insights into the pharmacological actions of WQD in GC treatment.

胃气汤治疗胃癌的机制:基于网络药理学的研究与实验验证。
背景:胃气汤(WQD)是中国传统治疗胃癌前病变的经验方。本研究旨在阐明WQD在GC治疗中的潜在药理机制。方法:利用公共数据库对有效成分、相应靶点及gc相关基因进行鉴定。通过STRING数据库构建蛋白-蛋白相互作用(PPI)网络,并使用DAVID平台进行功能富集分析。使用GEPIA数据库进行基因表达和生存分析。使用AutoDock Vina进行分子对接,并使用PyMOL进行可视化。通过CCK-8、菌落形成和Transwell试验评估WQD对GC细胞活力、增殖、迁移和侵袭的影响。结果:WQD含有43种有效成分,靶向751个潜在基因,其中gc相关靶点458个。槲皮素、木犀草素和山奈酚为主要活性成分。PPI网络分析揭示了9个核心靶点,包括TP53和SRC,它们可能介导WQD的抗gc作用。氧化石墨烯富集分析表明,氧化石墨烯参与了726个生物过程、91个细胞成分和177个分子功能,而KEGG通路分析表明,氧化石墨烯参与了AGE-RAGE、PI3K-Akt和HIF-1信号通路的调节。GEPIA数据库分析证实,EP300、HSP90AA1、HSP90AB1、SRC、TP53在GC中高表达。分子对接表明,关键活性化合物与核心靶点之间具有很强的结合亲和力。体外实验进一步验证了WQD提取物对胃癌细胞活力、增殖、迁移和侵袭的抑制作用。结论:WQD通过调节多种靶点和信号通路,具有治疗胃癌的潜力。这些发现为WQD在GC治疗中的药理作用提供了机制见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hereditas
Hereditas Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.80
自引率
3.70%
发文量
0
期刊介绍: For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.
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