Mechanism research on inhibition of gastric cancer

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Tác giả: Jun Chen, Fan Feng, Ping Hu, Chaoqun Lian, Lei Peng, Xingkui Tao, Luyao Wang

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: Poland : Open medicine (Warsaw, Poland) , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 664886

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, METHODS: Metabolomic analysis of two strains of gastric cancer cells treated with the 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.
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