基础医学与临床 ›› 2011, Vol. 31 ›› Issue (7): 767-772.

• 研究论文 • 上一篇    下一篇

姜黄素通过下调IκBα磷酸化抑制食管鳞癌细胞的体外增殖

田芳1,柴玉荣2,江亚南3,张晓艳2   

  1. 1. 郑州大学基础医学院病理生理学教研室
    2. 郑州大学基础医学院
    3. 郑州大学基础医学院病理生理教研室
  • 收稿日期:2010-06-17 修回日期:2010-08-30 出版日期:2011-07-05 发布日期:2011-07-05
  • 通讯作者: 田芳 E-mail:tianfang715@yahoo.com.cn
  • 基金资助:
    河南省医学科技攻关项目(编号:200803005);郑州市科技攻关项目(编号:0910SGYS33389-7)

The effect of curcumin through suppression of IκBα phosphorylation on proliferation of Esophageal Squamous Cell Carcinoma cell lines

Fang TIAN1,Yu-rong CHAI2,Ya-nan JIANG3,Xiao-yan ZHANG2   

  1. 1. School of Basic Medicine, Zhengzhou University
    2.
    3. Basic Medical College, Zhengzhou University
  • Received:2010-06-17 Revised:2010-08-30 Online:2011-07-05 Published:2011-07-05
  • Contact: Fang TIAN E-mail:tianfang715@yahoo.com.cn

摘要: 目的 探讨姜黄素是否能够通过下调IκBα的磷酸化,抑制食管鳞癌细胞的增殖并对其细胞周期产生影响。方法 MTT法检测姜黄素作用下食管鳞癌细胞的增殖;Western blot法检测EC9706和Eca109细胞在姜黄素作用下pIκBα和细胞周期蛋白cyclinD1的表达情况。两种细胞中加入姜黄素培养72h,或联合5-FU培养72h,流式细胞仪检测细胞周期。结果 EC9706和Eca109细胞的存活率均随着姜黄素浓度的增加逐渐下降;姜黄素作用下EC9706和Eca109细胞中pIκBα和cyclinD1蛋白的表达水平随着时间的延长逐渐下降,且G0/G1期的细胞开始增加,S期的细胞逐渐减少;当姜黄素联合使用5-FU时,G0/G1期的细胞明显增加, S期的细胞明显减少。结论 姜黄素通过下调IκBα及cyclinD1的表达,抑制食管鳞癌细胞的增殖,或许有望成为食管癌治疗中的一个辅助用药。

关键词: 食管鳞癌, 姜黄素, NF-κB, IκBα, cyclin D1

Abstract: Objective This study was to detect whether curcumin inhibits NF-κB signaling pathway through suppression IκBα phosphorylation and evaluate the effects on proliferation and cell cycle in EC9706 and Eca109 cell lines. Methods ESCC cells were treated with different concentrations of curcumin and then the number of viable cells were determined by MTT. Cytoplasmic extracts or whole cell extracts were examined for the expression of pIκBα and cyclinD1 using Western Blotting after treated with curcumin at different time. ESCC cells were treated with curcumin, 5-FU or combinations thereof for 72h. The cells were stained with PI and analyzed cell cycle by flow cytometry. Results The results showed that curcumin inhibited two ESCC cells growth in a concentration-dependent manner. The Western blotting results indicated that curcumin inhibited IκBα phosphorylation and downregulated the expression of cyclinD1 in the two ESCC cell lines in a time-dependent manner. CyclinD1 was declined in the forepart of curcumin-treated cells. Curcumin-treated cells showed an increase in the percentage of cells in the G0/G1 phase and a decrease in the percentage of cells in the S phase. While combination with 5-FU, the results were more prominence. Conclusion Therefore, curcumin inhibits the phosphorylation of IκBα and downregulates the activation of NF-κB signaling pathway, leading to suppression of proliferation in ESCC cell. Therefore, curcumin may prove useful in the treatment of ESCC because it is a pharmacologically safe compound without side effects.

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