外科理论与实践 ›› 2026, Vol. 31 ›› Issue (01): 70-76.doi: 10.16139/j.1007-9610.2026.01.12

• 论著 • 上一篇    下一篇

人参皂苷RG3通过PI3K/AKT/mTOR信号通路抑制胆囊癌细胞上皮间质转化

周忻1, 王路兵2, 章波2()   

  1. 1 上海中医药大学附属曙光医院检验科, 上海 200135
    2 上海健康医学院附属崇明医院普外科, 上海 202150
  • 收稿日期:2025-04-29 出版日期:2026-02-25 发布日期:2026-04-21
  • 通讯作者: 章波,E-mail: 15821992397@163.com
  • 作者简介:作者贡献/Authors’ contributions

    周忻、章波负责实验设计和操作以及文章撰写,王路兵负责实验结果统计和文献查阅。

  • 基金资助:
    上海市崇明区“可持续发展科技创新行动计划”项目(CKY2022-17)

Ginsenoside RG3 inhibits epithelial-mesenchymal transition of gallbladder cancer cells through PI3K/AKT/mTOR signaling pathway

ZHOU Xin1, WANG Lubing2, ZHANG Bo2()   

  1. 1 Department of Laboratory Medicine, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200135, China
    2 Department of Hepatobiliary Surgery, Chongming Hospital Affiliated to Shanghai University of Medicine and Health Sciences, Shanghai 202150, China
  • Received:2025-04-29 Online:2026-02-25 Published:2026-04-21

摘要:

目的:探索人参皂苷RG3抑制胆囊癌细胞的具体机制。方法:应用细胞计数试剂盒-8(CCK-8)实验,验证人参皂苷RG3对胆囊癌细胞活性的影响。通过细胞划痕实验和Transwell实验验证其对胆囊癌细胞迁移和侵袭的影响。通过蛋白质印迹实验验证其对上皮间质转化(EMT)相关蛋白质以及磷脂酰肌醇-3-激酶/蛋白激酶B/哺乳动物雷帕霉素靶蛋白[PI3K/PKB(AKT)/mTOR]信号通路相关蛋白质的影响。结果:人参皂苷RG3显著抑制胆囊癌细胞的活性,抑制细胞迁移的速率和Transwell实验中穿过小室的细胞数目。蛋白质印迹实验表明人参皂苷RG3显著降低磷酸化PI3K/AKT/mTOR蛋白的水平,上调E-钙黏着蛋白的表达水平,抑制N-钙黏着蛋白和波形蛋白的表达水平,最终抑制胆囊癌细胞EMT进程。结论:人参皂苷RG3抑制胆囊癌细胞活性,还通过调控PI3K/AKT/mTOR信号通路抑制胆囊癌细胞的EMT进程,抑制胆囊癌细胞迁移和侵袭。

关键词: 胆囊癌, 信号通路, 上皮间质转化, 人参皂苷RG3

Abstract:

Objective To explore the specific mechanism of Ginsenoside Rg3 inhibiting gallbladder cancer (GBC)cells. Methods Cell counting kit-8(CCK-8) assay was used to examine the effect of Ginsenoside Rg3 on the viability of GBC cells. The effect of Ginsenoside Rg3 on the migration and invasion of gallbladder cancer cells was verified by cell scratch assay and Transwell assay. Western blot was used to verify the effect of Ginsenoside Rg3 on epithelial-mesenchymal transition (EMT)-related proteins and phosphatidylinositol 3-kinase / protein kinase B (AKT) / mammalian target of rapamycin [PI3K/PKB(AKT)/mTOR] signaling pathway-related proteins. Results Ginsenoside Rg3 significantly inhibited the viability of GBC cells. Ginsenoside Rg3 significantly inhibited the rate of cell migration and the number of cells passing through the Transwell assay. Western blot showed that Ginsenoside Rg3 could significantly reduce the level of phosphorylated PI3K/AKT/mTOR protein, increase the expression level of E-cadherin, and inhibit the expression levels of N-cadherin and vimentin in gallbladder cancer cells, and finally inhibit the EMT process. Conclusions Ginsenoside RG3 inhibits the activity of gallbladder cancer cells, also suppresses the EMT process by regulating the PI3K/AKT/mTOR signaling pathway and inhibits the migration and invasion of gallbladder cancer cells.

Key words: Gallbladder cancer, Signaling pathway, Epithelial-mesenchymal transition(EMT), Ginsenoside Rg3

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