首页|复方葛根汤调控IL-6/STAT3和铁死亡通路抑制在体结肠癌发展

复方葛根汤调控IL-6/STAT3和铁死亡通路抑制在体结肠癌发展

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目的 探究复方葛根汤在体抗结肠癌的分子机制.方法 建立HCT116细胞荷瘤小鼠模型,每日以1.0g·kg-1的剂量灌胃给予复方葛根汤或等体积生理盐水,每3日测量一次体重和瘤体大小,连续给药23 d;Western blot检测铁死亡通路、IL-6通路和细胞迁移相关蛋白.结果 与对照组相比,复方葛根汤显著抑制HCT116细胞衍生瘤体增长,显著上调铁死亡相关蛋白 ACSL4、PTGS2,而明显下调 SLC7A11、GPX4,还显著下调 IL-6、p-STAT3/STAT3 比及其下游蛋白MMP2、TWIST和MMP7水平.结论 复方葛根汤能显著抑制体内结肠癌发展,其机制可能为通过抑制IL-6/STAT3和诱导铁死亡通路.
Inhibition effect of Compound Gegen decoction on the development of colon cancer in vivo by regulating IL-6/STAT3 and ferroptosis pathway
Objective To determine the molecular mechanism of Compound Gegen decoction(CGD)inhibiting colon cancer in vivo.Methods The HCT116 cell-derived tumor bearing mouse model was established and daily given CGD or equal volume saline intragastrically at the dose of 1.0 g·kg-1 for 23 days,and the weight and tumor size were measured once every three days.The ferroptosis pathway,IL-6 pathway and cell migration-related proteins were detected by Western blot.Results Compared with the control group,CGD greatly inhibited the growth of HCT116 cell-derived tumor in vivo.Ferroptosis-related proteins ACSL4 and PTGS2 were much up-regulated,while SLC7A11 and GPX4 were obviously down-regulated,and IL-6,p-STAT3/STAT3 ratio and its downstream proteins MMP2,TWIST and MMP7 were all greatly down-regulated.Conclusion CGD can inhibit the growth of colon cancer in vivo,whose mechanism may be through inhibiting IL-6/STAT3 and inducing ferroptosis pathway.

Compound Gegen decoctioncolon cancer in vivoIL-6/STAT3 pathwayferroptosis

钱玲、赵斌、饶江泉、徐恩惠、陈慧、杨潮、罗小泉、陈来

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江西中医药大学,南昌 330004

江西省癌症技术转化工程研究中心,南昌 330004

江西省中药药理重点实验室,南昌 330004

复方葛根汤 在体结肠癌 IL-6/STAT3通路 铁死亡

江西省卫生与健康委员会科技项目江西省科技计划江西省中医药局科技项目

20221141920212BCD460052022B1051

2024

中南药学
湖南省药学会

中南药学

CSTPCD
影响因子:0.736
ISSN:1672-2981
年,卷(期):2024.22(4)
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