Mechanism research on inhibition of gastric cancer in vitro by the extract of Pinellia ternata based on network pharmacology and cellular metabolomics.

IF 1.7 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Open Medicine Pub Date : 2025-02-18 eCollection Date: 2025-01-01 DOI:10.1515/med-2024-1131
Fan Feng, Ping Hu, Jun Chen, Lei Peng, Luyao Wang, Xingkui Tao, Chaoqun Lian
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引用次数: 0

Abstract

Background and purpose: Gastric cancer is a kind of malignant tumor with high incidence and high mortality, which has strong tumor heterogeneity. A classic Chinese medicine, Pinellia ternata (PT), was shown to exert therapeutic effects on gastric cancer cells. However, its chemical and pharmacological profiles remain to be elucidated. In the current study, we aimed to reveal the mechanism of PT in treating gastric cancer cells through metabolomic analysis and network pharmacology.

Methods: Metabolomic analysis of two strains of gastric cancer cells treated with the Pinellia ternata extract (PTE) was used to identify differential metabolites, and the metabolic pathways were enriched by MetaboAnalyst. Then, network pharmacology was applied to dig out the potential targets against gastric cancer cells induced by PTE. The integrated network of metabolomics and network pharmacology was constructed based on Cytoscape.

Results: The PTE was confirmed to significantly inhibit cell proliferation, migration, and invasion of HGC-27 and BGC-823 cells. The results of cellular metabolomics showed that 61 metabolites were differently expressed in gastric cancer cells of the experimental and control groups. Through pathway enrichment analysis, 16 metabolites were found to be involved in the glycerophospholipid metabolism, purine metabolism, sphingolipid metabolism, and tryptophan metabolism. Combined with network pharmacology, seven bioactive compounds were found in PT, and the networks of bioactive compound-target gene-metabolic enzyme-metabolite interactions were constructed.

Conclusions: In conclusion, this study revealed the complicated mechanisms of PT against gastric cancer. Our work provides a novel paradigm to identify the potential mechanisms of pharmacological effects derived from a natural compound.

基于网络药理学和细胞代谢组学的半夏提取物体外抑制胃癌的机制研究。
背景与目的:胃癌是一种高发病率、高死亡率的恶性肿瘤,具有较强的肿瘤异质性。经典中药半夏(Pinellia ternata, PT)被证明对胃癌细胞有治疗作用。然而,其化学和药理特征仍有待阐明。在本研究中,我们旨在通过代谢组学分析和网络药理学来揭示PT治疗胃癌细胞的机制。方法:对两株经半夏提取物(PTE)处理的胃癌细胞进行代谢组学分析,鉴定差异代谢物,并用MetaboAnalyst富集代谢途径。然后,应用网络药理学方法挖掘PTE诱导胃癌细胞的潜在靶点,基于Cytoscape构建代谢组学与网络药理学的整合网络。结果:PTE对HGC-27、BGC-823细胞的增殖、迁移、侵袭均有明显抑制作用。细胞代谢组学结果显示,实验组和对照组胃癌细胞中有61种代谢物表达不同。通过通路富集分析,发现16种代谢物参与了甘油磷脂代谢、嘌呤代谢、鞘脂代谢和色氨酸代谢。结合网络药理学,在PT中发现了7种生物活性化合物,构建了生物活性化合物-靶基因-代谢酶-代谢物相互作用的网络。结论:本研究揭示了PT抗胃癌的复杂机制。我们的工作提供了一个新的范例,以确定来自天然化合物的药理作用的潜在机制。
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
Open Medicine
Open Medicine Medicine-General Medicine
CiteScore
3.00
自引率
0.00%
发文量
153
审稿时长
20 weeks
期刊介绍: Open Medicine is an open access journal that provides users with free, instant, and continued access to all content worldwide. The primary goal of the journal has always been a focus on maintaining the high quality of its published content. Its mission is to facilitate the exchange of ideas between medical science researchers from different countries. Papers connected to all fields of medicine and public health are welcomed. Open Medicine accepts submissions of research articles, reviews, case reports, letters to editor and book reviews.
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