ISSN 1004-6879

CN 13-1154/R

 

Journal of Chengde Medical University ›› 2022, Vol. 39 ›› Issue (6): 451-455.

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Effects of PU-H71 on Apoptosis and Cycle of HCT-15 Cells in Colorectal Cancer

TIAN Duo-duo1, DENG Cheng1, ZHAO Xue-rong1, WANG Jian-ping1, ZHENG Hua-chuan2, XIAO Li-jun1,*, ZHAO En-hong2   

  1. 1. Basic Medical Institute Chengde Medical University, Chengde, Hebei, 067000, China;
    2. Affiliated Hospital of Chengde Medical University, Chengde, Hebei, 067000, China
  • Received:2021-11-30 Online:2022-12-10 Published:2023-04-10

PU-H71对结直肠癌HCT-15细胞凋亡和周期的影响

田朵朵1, 邓程1, 赵学荣1, 王建平1, 郑华川2, 肖丽君1,*, 赵恩宏2   

  1. 1.承德医学院基础医学院,河北承德 067000;
    2.承德医学院附属医院
  • 通讯作者: *
  • 基金资助:
    河北省教育厅课题(ZD20180004,QN2016017,QN2020208); 河北省医学科学研究课题(20160009,20211467,20210691); 承德医学院校级课题(202014,201806)

Abstract: Objective To study the effects of PU-H71 on the proliferation, apoptosis, cycle and other biological behaviors of colorectal cancer HCT-15 cells, and to explore the mechanism of apoptosis and cycle at the molecular level. Methods HCT-15 cells were cultured in vitro. The effects of PU-H71 at different time and concentration on the proliferation of HCT-15 cells were examined by MTT assay. The apoptosis and cell cycle of HCT-15 cells were examined by flow cytometry assay, western blot was used to detect the expression of apoptosis and cycle-related factors. Results After 24h and 48h treatment, PU-H71 showed significant inhibitory effect on colorectal cancer HCT-15 cells in time and concentration dependent manner. After treatment with PU-H71 at two concentrations of 50μg/L and 75μg/L without drug for 24h, the apoptosis rate of HCT-15 cells increased and the proportion of G2 phase cells increased. The protein expression levels of STAT3 and JAK2 were significantly decreased, the protein expression levels of CyclinD1 and Bcl-2 were decreased, and the protein expression levels of Cytc, Caspase9, Caspase3, and Bax were up-regulated. Conclusion PU-H71 can significantly inhibit the proliferation of colorectal cancer HCT-15 cells, arrest the cell cycle in G2 phase and induce cell apoptosis. PU-H71 may regulate the mitochondrial signaling pathway by negatively regulating the JAK-STAT3 pathway, thus affecting the expression of apoptosis and cyclic-related factors.

Key words: PU-H71, HCT-15, cell apoptosis, cell cycle, colorectal cancer

摘要: 目的 探究PU-H71对结直肠癌HCT-15细胞增殖、凋亡、周期等生物学行为的影响,在分子水平探讨HCT-15细胞凋亡和周期的作用机制。方法 体外培养人结直肠腺癌HCT-15细胞,MTT检测不同时间点和浓度的PU-H71对结直肠癌HCT-15细胞增殖的作用;流式细胞术检测细胞凋亡和周期;Western blot 检测相关因子的表达水平。结果 PU-H71作用24h和48h后,对结直肠癌HCT-15细胞有显著的抑制作用,并有明显的时间和浓度依赖性;设置不同浓度组作用24h后,HCT-15细胞凋亡率上升且处于G2期的细胞增多;STAT3和JAK2蛋白的表达水平明显下降,周期及凋亡相关因子CyclinD1和Bcl-2蛋白表达水平下降,Cytc、Caspase9、Caspase3、Bax蛋白表达水平上调。结论 PU-H71对结直肠癌HCT-15细胞的增殖有明显的抑制作用,使细胞G2周期阻滞并诱导凋亡。PU-H71有可能通过负向调控JAK-STAT3途径来调控线粒体信号通路,以此影响凋亡和周期相关因子的表达。

关键词: PU-H71, HCT-15细胞, 细胞凋亡, 细胞周期

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