癌变·畸变·突变 ›› 2008, Vol. 20 ›› Issue (6): 445-448.doi: 10.3969/j.issn.1004-616x.2008.06.007

• 论著 • 上一篇    下一篇

香加皮宝霍甙-Ⅰ诱导人食管癌细胞Eca-109凋亡的实验研究

刘晓霞1,单保恩2,陈育民1,任风芝3,商晓辉1   

  1. 1.河北工程大学医学院,河北 邯郸 056029;2.河北医科大学第四医院科研中心,河北 石家庄 050011;3. 华北制药集团新药研究开发有限责任公司,河北 石家庄 050015
  • 收稿日期:2008-04-30 修回日期:2008-05-09 出版日期:2008-11-30 发布日期:2008-11-30

Effect of Baohuoside-Ⅰ on Apoptosis of Human Esophageal Carcinoma Cell Eca-109

LIU Xiao-xia1, SHAN Bao-en2,, CHEN Yu-min1, REN Feng-zhi3, SHANG Xiao-hui1   

  1. 1. Medical College of Hebei University of Engineering, Handan 056029 Hebei, China; 2. Research Center, Fourth Hospital of Hebei Medical University, Shijiazhuang 050011 Hebei, China; 3. New Drug Research and Development Co. Ltd. of North China Pharmaceutical Corporation, Shijiazhuang 050015, Hebei, China
  • Received:2008-04-30 Revised:2008-05-09 Online:2008-11-30 Published:2008-11-30

摘要: 背景与目的: 研究香加皮宝霍甙-Ⅰ诱导人食管癌细胞Eca-109的凋亡作用及其作用机制。 材料与方法: 采用MTT法分析不同浓度(12.5、25、50 μg/ml)宝霍甙-Ⅰ分别作用Eca-109细胞24 h、48 h、72 h后,对细胞增殖的抑制作用;经不同浓度(12.5、25、50 μg/ml)宝霍甙-Ⅰ作用Eca-109细胞48 h后,用流式细胞术分析细胞凋亡率及凋亡相关蛋白Survivin的表达;用透射电镜观察凋亡细胞的超微结构变化;用RT-PCR技术检测Survivin mRNA的表达。 结果: 不同浓度宝霍甙-Ⅰ均可明显抑制Eca-109细胞的增殖 (P均<0.05)且随浓度的增加和作用时间的延长抑制作用增强,作用48 h后的半数抑制浓度IC50为24.8 μg/ml。不同浓度宝霍甙-Ⅰ作用48 h后,均可诱导Eca-109细胞凋亡,50 μg/ml时细胞凋亡率达55.26%,且导致Eca-109细胞发生凋亡特征性超微结构改变,并使Eca-109细胞Survivin mRNA和蛋白表达水平均明显降低(P<0.01)。 结论: 香加皮宝霍甙-Ⅰ可抑制Eca-109细胞增殖,诱导细胞凋亡,该作用可能与下调细胞Survivin表达有关。

关键词: 食管癌, 香加皮宝霍甙-Ⅰ, 细胞凋亡, 基因表达

Abstract: BACKGROUND AND AIM: Effect of baohuoside-Ⅰ from Cortex Periplocae on apoptosis of human esophageal carcinoma cell Eca-109 and its mechanism were studied. MATERIALS AND METHODS: After treatment with baohuoside-Ⅰ at different concentrations (12.5, 25, 50 μg/ml)for 24 h, 48 h, 72 h, the inhibitory effect on proliferation of Eca-109 cells was analyzed by MTT method.After treatment with baohuoside-Ⅰ under different concentrations(12.5、25、50 μg/ml) for 48 h, cell apoptotic ratio and expression of Eca-109 cells Survivin protein of were measured with flow cytometry (FCM); the ultrastructure was examined by transmission electron microscope; the expression of Survivin mRNA was detected by RT-PCR. RESULTS: Baohuoside-Ⅰ significantly inhibited proliferation of Eca-109 cells, and in concentration- dependent manner(P all<0.05), the IC50 was 24.8 μg/ml. After treatment with different concentrations of Baohuoside-Ⅰfor 48 h, cell apoptosis of Eca-109 cells was induced significantly (the apoptotic ratio is 55.26% treated with 50 μg/ml of baohuoside-Ⅰ) and showing characteristic ultrastructural changes of apoptosis. Expression levels of Survivin mRNA and protein were decreased significantly(P<0.01). CONCLUSION: Baohuoside-Ⅰ of Cortex Periplocae could inhibit the proliferation and induce apoptosis of Eca-109 cell. This effect was associated with down-regulation of Survivin mRNA expression.

Key words: human esophageal carcinoma, baohuoside-, apoptosis, gene expression