基础医学与临床 ›› 2020, Vol. 40 ›› Issue (3): 340-345.

• 研究论文 • 上一篇    下一篇

牛磺酸联合SN50协同抑制人肝癌细胞系HepG2的增殖

雷巧丽1*, 饶奇斌2, 林泽文1   

  1. 1.深圳市龙华区人民医院, 广东 深圳 518109;
    2.深圳市罗湖医院集团, 广东 深圳 518023
  • 收稿日期:2019-04-12 修回日期:2019-09-27 出版日期:2020-03-05 发布日期:2020-03-02
  • 通讯作者: *2095742729@qq.com
  • 基金资助:
    深圳市科技创新基础研究项目(JCYJ201704221524)

Taurine combined with SN50 inhibits the proliferation of human hepatocellular carcinoma cell line HepG2

LEI Qiao-li1*, RAO Qi-bin2, LIN Ze-wen1   

  1. 1. Shenzhen Longhua District People's Hospital, Shenzhen 518109;
    2. Shenzhen Luohu Hospital Group, Shenzhen 518023,China
  • Received:2019-04-12 Revised:2019-09-27 Online:2020-03-05 Published:2020-03-02
  • Contact: *2095742729@qq.com

摘要: 目的 探讨牛磺酸联合NF-κB信号通路抑制剂SN50对肝癌细胞系HepG2增殖的影响及其机制。方法 将HepG2细胞分为对照组、牛磺酸组(给予150 mmol/L牛磺酸处理24 h)、抑制剂组(给予36 μmol/L SN50处理24 h)和牛磺酸+抑制剂组;用MTT法、克隆形成实验和流式细胞仪分别检测细胞的增殖和凋亡;Western blot和RT-qPCR检测细胞中cyclin D1、Bcl-2蛋白和mRNA的表达情况。结果 与对照组相比,经150 mmol/L牛磺酸或36 μmol/L SN50处理24 h后,HepG2细胞的生存率和集落形成率均明显降低,凋亡率明显升高,细胞中cyclin D1和Bcl-2蛋白和mRNA表达均明显受到抑制(P<0.05)。同时,SN50增强了牛磺酸对HepG2细胞的增殖和cyclin D1、Bcl-2表达的抑制作用以及对细胞凋亡的促进作用。结论 牛磺酸联合NF-κB信号通路抑制剂协同抑制肝癌细胞系HepG2的增殖。

关键词: 肝癌, 牛磺酸, NF-κB信号通路, 细胞增殖, 凋亡

Abstract: Objective To investigate the effect of taurine combined with NF-κB signaling pathway inhibitor SN50 on the proliferation of hepatocellular carcinoma cells line HepG2 and its mechanism. Methods The expression of p-IκBα and IκBα proteins in hepatoma cells line HepG2 was detected by Western blot after the treatment with 150 mmol/L taurine for 24 hours. HepG2 cells were randomly divided into control group (untreated), taurine group (treated with 150 mmol/L taurine for 24 hours), inhibitor group (treated with 36 μmol/L SN50 for 24 hours) and taurine + inhibitor group (treated with 150 mmol/L taurine and 36 μmol/L SN50 for 24 hours), cell proliferation and apoptosis were examined by MTT, colony forming test and flow cytometry respectively,and cyclin D1, Bcl-2 protein and mRNA were detected by Western blot and RT-qPCR. Results After treatment with 150 mmol/L taurine for 24 hours, the expression of p-IκBα protein in HepG2 cells decreased in a time-dependent manner (P<0.05). After treatment with 150 mmol/L taurine or 36 μmol/l SN50 for 24 hours, the survival rate and cloning rate of HepG2 cells significantly decreased, the apoptosis rate significantly increased, and the expressions of cyclin D1 and Bcl-2 protein and mRNA were significantly inhibited as compared with the control group, all the differences were statistically significant(P<0.05).At the same time, SN50 enhanced the inhibitory effect of taurine on the proliferation of HepG2 cells, the expression of cyclin D1 and Bcl-2, and the promotion of apoptosis. Conclusions Combined efforts of taurine with NF-κB signaling pathway inhibitor SN50 inhibit strongly the proliferation of hepatoma cells line HepG2 through NF-κB signaling pathway.

Key words: hepatocellular carcinoma, taurine, NF-κB signaling pathway, cell proliferation, apoptosis

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