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薯蓣皂苷元通过调节DAXX亚细胞定位激活JNK/p38信号通路诱导MCF-7细胞凋亡

王佳, 高世磊, 张丽菡, 张璐, 孙旭, 李华华, 刘怀民

王佳, 高世磊, 张丽菡, 张璐, 孙旭, 李华华, 刘怀民. 薯蓣皂苷元通过调节DAXX亚细胞定位激活JNK/p38信号通路诱导MCF-7细胞凋亡[J]. 肿瘤防治研究. DOI: 10.3971/j.issn.1000-8578.20240980
引用本文: 王佳, 高世磊, 张丽菡, 张璐, 孙旭, 李华华, 刘怀民. 薯蓣皂苷元通过调节DAXX亚细胞定位激活JNK/p38信号通路诱导MCF-7细胞凋亡[J]. 肿瘤防治研究. DOI: 10.3971/j.issn.1000-8578.20240980
Jia WANG, Shi-lei GAO, Li-han ZHANG, Lu ZHANG, Xu SUN, Hua-hua LI, Huai-min LIU. Diosgenin Induces Apoptosis of MCF-7 Cells by Regulating DAXX Subcellular Localization and Activating JNK/p38 Signaling Pathway[J]. Cancer Research on Prevention and Treatment. DOI: 10.3971/j.issn.1000-8578.20240980
Citation: Jia WANG, Shi-lei GAO, Li-han ZHANG, Lu ZHANG, Xu SUN, Hua-hua LI, Huai-min LIU. Diosgenin Induces Apoptosis of MCF-7 Cells by Regulating DAXX Subcellular Localization and Activating JNK/p38 Signaling Pathway[J]. Cancer Research on Prevention and Treatment. DOI: 10.3971/j.issn.1000-8578.20240980

薯蓣皂苷元通过调节DAXX亚细胞定位激活JNK/p38信号通路诱导MCF-7细胞凋亡

基金项目: 河南省自然科学基金;国家自然科学基金

Diosgenin Induces Apoptosis of MCF-7 Cells by Regulating DAXX Subcellular Localization and Activating JNK/p38 Signaling Pathway

  • 摘要: 目的 探讨薯蓣皂苷元对乳腺癌细胞增殖和凋亡的影响及潜在的分子机制。方法 以低、中、高剂量的薯蓣皂苷元作用于乳腺癌细胞MCF-7,MMT法检测细胞增殖力;流式细胞术检测细胞凋亡;核-浆蛋白分离法和免疫荧光检测死亡结构域相关蛋白(DAXX)亚细胞定位;qRT-PCR和western blot检测DAXX和c-Jun N末端激酶通路(JNK)相关蛋白表达水平。结果 薯蓣皂苷元可以显著抑制MCF-7细胞增殖、促进其凋亡,且呈现出一定的浓度依赖性,薯蓣皂苷元能够促进DAXX由细胞核进入细胞浆,并且上调细胞表面死亡受体(Fas)表达,提高JNK和丝裂原活化蛋白激酶(p38)的磷酸化水平,激活JNK/p38信号通路。结论 薯蓣皂苷元抑制乳腺癌细胞MCF-7细胞增殖并促进其凋亡,其作用机制可能与调节DAXX亚细胞定位、激活JNK/p38信号通路有关。

     

    Abstract: Objective To investigate the effect of diosgenin on proliferation and apoptosis of breast cancer cells and its potential molecular mechanism. Methods The breast cancer cell line MCF-7 was treated with low, medium and high doses of diosgenin, the cell proliferation was detected by MMT method. Flow cytometry was used to detect cell apoptosis. Nuclear cytoplasmic protein separation method and immunofluorescence were applied to detect the subcellular localization of death associated protein (DAXX). qRT-PCR and western blot were used to detect the expression of DAXX and c-Jun N-terminal kinase pathway (JNK) related protein. Results diosgenin significantly inhibit the proliferation of MCF-7 cells and promote their apoptosis with concentration dependence. Diosgenin promoted DAXX moving from nucleus into cytoplasm, upregulated the expression of cell surface death receptor (Fas), increased the phosphorylation levels of JNK and mitogen activated protein kinase (p38), and activated the JNK/p38 signaling pathway. Conclusion Diosgenin inhibits the proliferation and apoptosis of breast cancer cell line MCF-7, whose mechanism might be related to the regulation of DAXX subcellular localization and the activation of JNK/p38 signaling pathway.

     

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出版历程
  • 收稿日期:  2024-10-08
  • 修回日期:  2025-01-17
  • 录用日期:  2025-02-19
  • 网络出版日期:  2025-03-04

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