首页 | 本学科首页   官方微博 | 高级检索  
检索        

依地福新对Hela细胞生长的抑制作用及其机制研究
引用本文:张辉,喻莉萍,周菊锋,何笃贵,李林珍,王彬,罗桐秀,李强国.依地福新对Hela细胞生长的抑制作用及其机制研究[J].中国药房,2008,19(22):1705-1707.
作者姓名:张辉  喻莉萍  周菊锋  何笃贵  李林珍  王彬  罗桐秀  李强国
作者单位:湘南学院,郴州市,423000
摘    要:目的:观察依地福新对人宫颈癌Hela细胞的体外生长抑制作用,并进一步探讨其作用机制。方法:细胞中分别加入不同浓度的依地福新(0.5、1.0、5.0、10.0μmol.L-1)处理96h,并设立未加依地福新的对照组。应用MTT法检测细胞增殖活性;流式细胞仪检测细胞周期分布;染色法检测细胞凋亡率。结果:与对照组比较,不同浓度依地福新处理Hela细胞24~96h后,细胞增殖显著受到抑制,并呈浓度及时间依赖性;1.0、5.0、10.0μmol.L-1浓度依地福新处理72h后,Hela细胞G0/G1期细胞数量显著增加,S期细胞数量显著降低(P<0.01);各浓度组细胞凋亡率均显著增加(P<0.01)。结论:依地福新对Hela细胞具有生长抑制作用,其机制可能与阻滞细胞周期及诱导凋亡有关。

关 键 词:依地福新  Hela细胞  凋亡

Effect of Edelfosine on the Proliferation of Hela Cells and Its Mechanism
ZHANG Hui,YU Li-ping,ZHOU Ju-feng,HE Du-gui,LI Lin-zhen,WANG Bin,LUO Tong-xiu,LI Qiang-guo.Effect of Edelfosine on the Proliferation of Hela Cells and Its Mechanism[J].China Pharmacy,2008,19(22):1705-1707.
Authors:ZHANG Hui  YU Li-ping  ZHOU Ju-feng  HE Du-gui  LI Lin-zhen  WANG Bin  LUO Tong-xiu  LI Qiang-guo
Institution:(Xiangnan University, Chenzhou 423000, China)
Abstract:OBJECTIVE: To investigate the effect of edelfosine on the proliferation of Hela cells and its mechanism. METHODS: Hela cells were treated with edelfosine at doses of 0 (control), 0.5, 1.0, 5.0, 10.0 μmol·L^-1 for 96 h. MTT assay, flow cytometry, and staining were performed to determine the cell proliferation activity, cell cycle, and apoptotic rate. RESULTS: As compared with control, the cell proliferation activity of Hela cells was inhibited in a dose and time dependent manner after being treated by edelfosine for 24--96 h. After being treated by edelfosine (1.0, 5.0, 10.0 μmol·L^-1) for 72 h, the number of Hela cells significantly increased in G0/G1 phase but decreased in S phase (P 〈 0.01); and the apoptotic rate of Hela cells in different concentrations of edelfosine increased significantly (P 〈 0.01). CONCLUSION: Edelfosine could inhibit the growth of Hela cells by blocking cell cycle and inducing apoptosis.
Keywords:Edelfosine  Hela cell  Apoptosis
本文献已被 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号