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苦参碱诱导人肺鳞癌SK-MES-1细胞凋亡作用及其可能机制
引用本文:金晨慈,蒋龙翔. 苦参碱诱导人肺鳞癌SK-MES-1细胞凋亡作用及其可能机制[J]. 温州医学院学报, 2010, 40(1): 39-42
作者姓名:金晨慈  蒋龙翔
作者单位:温州市中西医结合医院,呼吸科,浙江,温州,325000
摘    要:目的:探讨苦参碱(MT)诱导人肺鳞癌细胞株SK-MES-1凋亡作用及其抗肿瘤机制。方法:培养人肺鳞癌细胞株SK-MES-1,用不同浓度的MT处理SK-MES-1细胞,用MTT法检测MT对SK-MES-1细胞生长增殖的抑制作用;流式细胞术检测细胞凋亡率和细胞周期;流式细胞术检测细胞相关凋亡蛋白Bcl-2、bax、caspase-3表达。结果:MT抑制SK-MES-1细胞增殖和诱导SK-MES-1细胞的凋亡作用均呈剂量和时间依赖性。与对照组相比,苦参碱处理后的SK-MES-1细胞G0/G1期百分比明显增高,S期细胞比例下降。Bax和capase-3表达增强,Bcl-2表达下调。结论:MT在体外能抑制人肺鳞癌细胞株SK-MES-1增殖,诱导细胞凋亡,其诱导作用具有明显的量效和时效关系,可能与抑制Bcl-2活性、激活bax和capase-3有关。

关 键 词:苦参碱  肺鳞癌  细胞凋亡  SK-MES-1

Matrine-induced apoptosis in human lung squamous cell carcinoma SK-MES-1 cells and the possible mechanism
JIN Chenci,JIANG Longxiang. Matrine-induced apoptosis in human lung squamous cell carcinoma SK-MES-1 cells and the possible mechanism[J]. Journal of Wenzhou Medical College, 2010, 40(1): 39-42
Authors:JIN Chenci  JIANG Longxiang
Affiliation:. Department of Respiratory Medicine,Wenzhou Integrated TCM & Western Medicine Hospital,Wenzhou,325000
Abstract:Objective:To explore the effects of matrine on the cell cycle and apoptosis in human lung squamous cell carcinoma SK-MES-1 cells and explore the possible mechanisms.Methods:The effect of matrine on cell proliferation was assessed using MTT assay.The cell cycle arrest and the apoptosis rate induced by matrine were determined with flow cytometry.The expression of caspase-3,Bcl-2 and Bax proteins were assayed by flow cytometry.Results:Matrine inhibited the proliferation of SK-MES-1 cells in a dose-and time-dependent manner.Compared with the control group,the matrine-treated cells showed increased cell percentage arrested in G0/G1 phase with decreased S-phase cells.After treatment of 48 hours,the apoptosis rate was increased.The expression of caspase-3 and Bax increased.The expression of Bcl-2 decreased.Conclusion:Matrine can inhibit SK-MES-1 cell proliferation,cause cell cycle arrest at G0/G1 phase,and induce apoptosis in a dose-and time-dependent manner,which may be related to activation of caspase-3 and Bax and suppression of Bcl-2.
Keywords:SK-MES-1
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