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蟾毒灵对人乳腺癌MDA-MB-231细胞增殖和凋亡的作用

Effect of bufalin on proliferation and apoptosis of human breast cancer MDA-MB-231 cells
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摘要 目的探讨蟾毒灵在体外对人乳腺癌MDA-MB-231细胞增殖和凋亡的作用及初步机制。方法以不同浓度的蟾毒灵处理MDA-MB-231细胞,MTT法检测细胞存活率,流式细胞术检测细胞凋亡水平,2',7'-二氯荧光黄双乙酸盐法测定活性氧(ROS)水平,RT-PCR检测细胞凋亡相关基因Bax和Bcl-2mRNA表达水平。结果蟾毒灵可剂量依赖性地降低MDA-MB-231细胞的存活率,诱导细胞凋亡(P<0.01)。蟾毒灵处理细胞后,细胞内ROS水平增加(P<0.01),Bax mRNA表达增加,而Bcl-2 mRNA表达减少(P<0.05或P<0.01)。结论蟾毒灵在体外能抑制人乳腺癌MDA-MB-231细胞的增殖,诱导细胞凋亡,该作用可能与其升高细胞内ROS水平、上调Bax/Bcl-2的比例有关。 Objective To investigate the effect of bufalin on human breast cancer MDA-MB-231 cells proliferation and apoptosis in vitro and its related molecular mechanism.Methods After MDA-MB-231 cells were cultured and treated with different concentrations of bufalin,the cell survival rate was measured by MTT,the cell apoptosis was analyzed by flow cytometry,the content of reactive oxygen species(ROS)was examined by 2',7'-dichlorofluorescein diacetate assay,and the mRNA expressions of Bax and Bcl-2 were detected by RT-PCR,respectively.Results With bufalin treatment,the survival rate of MDA-MB-231 cells was decreased in a dose-dependent manner and the apoptosis was induced (P〈0.01).Bufalin could increase the level of ROS(P〈0.01),and upregulate the expression of Bax and downregulate the expression of Bcl-2 at the mRNA level(P〈0.05 or P〈0.01).Conclusion Bufalin is able to inhibit the proliferation and induce apoptosis of MDA-MB-231 cells in vitro,and the possible mechanism may be related with the effect of increasing ROS level and upregulating the ratio of Bax/Bcl-2.
作者 李静 LI Jing(Wuxi Higher Health Vocational Technology School, Wuxi 214028, CHINA)
出处 《江苏医药》 CAS 2017年第23期1674-1677,共4页 Jiangsu Medical Journal
关键词 蟾毒灵 乳腺癌 细胞凋亡 细胞增殖 Bufalin Breast cancer Cell apoptosis Cell proliferation
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  • 1赵建斌,崔勤,王文亮,蒋永培.蟾毒灵诱导人急性早幼粒细胞性白血病细胞凋亡的实验观察[J].解放军药学学报,2004,20(3):161-163. 被引量:15
  • 2张德芹,张建军,钟赣生,王景霞,胡素敏,高学敏.芪蓝糖脂宁胶囊对糖尿病合并高脂血症大鼠肝细胞凋亡及Bax、Bcl-2蛋白表达的影响[J].中华中医药杂志,2005,20(4):211-213. 被引量:24
  • 3[1]Zou H, Li Y, Liu X et al. An Apaf-1.cytochrome C multimeric complex is a functional apoptosome that activates procaspase-9. J Biol Chem, 1999; 274 (17): 11549~56
  • 4[2]Hu Y, Benedict MA, Ding L et al. Role of cytochrome C and dATP/ATP hydrolysis in Apaf-1-mediated caspase-9 activation and apoptosis. EMBO J, 1999; 18 (13): 3586~95
  • 5[3]Saleh A, Srinivasula SM, Acharya S et al. Cytochrome C and dATP-mediated oligomerization of Apaf-1 is a prerequisite for procaspase-9 activation. J Biol Chem, 1999; 274 (25): 17941~5
  • 6[4]Enari M, Sakahira H, Yokoyama H et al. A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD. Nature, 1998; 391 (6662): 43~50
  • 7[5]Liu X, Kim CN, Yang J et al. Induction of apoptotic program in cell-free extracts:Requirement for dATP and cytochrome C. Cell, 1996; 86 (1): 147~57
  • 8[6]Pandey P, Saleh A, Nakazawa A et al. Negative regulation of cytochrome C-mediated oligomerization of Apaf-1 and activation of procaspase-9 by heat shock protein 90. EMBO J, 2000; 19 (16): 4310~22
  • 9[7]Goldstein JC, Waterhouse NJ, Juin P et al. The coordinate release of cytochrome C during apoptosis is rapid, complete and kinetically invariant. Nat Cell Biol, 2000; 2 (3): 156~62
  • 10[8]Marzo I, Brenner C, Zamzami N et al. Bax and adenine nucleotide translocator cooperate in the mitochondrial control of apoptosis. Science, 1998; 281 (5385): 2027~31

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