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基于网络药理学和分子对接技术,山奈酚通过靶向AKT/GSK3β信号通路抑制胃癌细胞的侵袭和转移。

Kaempferol inhibited invasion and metastasis of gastric cancer cells by targeting AKT/GSK3β pathway based on network pharmacology and molecular docking.

作者信息

Gao Xia-Qing, Li Hai-Long, Wang Meng, Yang Chun-Ting, Su Rong, Shao Li-Hua

机构信息

The First Clinical Medical College, Gansu University of Chinese Medicine, Lanzhou 730000, China.

Key Laboratory of Gansu Provincial Prescription Mining and Innovative Translational Laboratory, Gansu University of Chinese Medicine, Lanzhou 730000, China.

出版信息

J Asian Nat Prod Res. 2025 Mar;27(3):421-441. doi: 10.1080/10286020.2024.2387756. Epub 2024 Aug 12.

Abstract

This study aims to explore the mechanisms of the inhibitory effect of kaempferol on the invasion and metastasis of gastric cancer (GC) cells through network pharmacology prediction and experimental verification. It identifies core targets via PPI network analysis and finds that kaempferol binds to these targets well. experiments showed that kaempferol could inhibit the proliferation, colony formation, migration and invasion of GC cells. Western blotting indicated kaempferol may reduce AKT and GSK3β phosphorylation, leading to lower expression of invasion-related genes SRC, MMP9, CXCR4, KDR, and MMP2. Overall, kaempferol may prevent migration and invasion of GC cells via the AKT/GSK3β signaling pathway.

摘要

本研究旨在通过网络药理学预测和实验验证,探索山奈酚对胃癌(GC)细胞侵袭和转移的抑制作用机制。通过蛋白质-蛋白质相互作用(PPI)网络分析确定核心靶点,并发现山奈酚与这些靶点结合良好。实验表明,山奈酚可抑制GC细胞的增殖、集落形成、迁移和侵袭。蛋白质免疫印迹法表明,山奈酚可能降低AKT和GSK3β的磷酸化水平,导致侵袭相关基因SRC、MMP9、CXCR4、KDR和MMP2的表达降低。总体而言,山奈酚可能通过AKT/GSK3β信号通路阻止GC细胞的迁移和侵袭。

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