ZHANG Xue-mei,YANG Xiu-rong,WU Hua,ZHANG Zhen-wei,XIANYU Zhi-qun.The apoptotic pathway of breast cancer multidrug resistant cells[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(15):1475-1478.
ZHANG Xue-mei,YANG Xiu-rong,WU Hua,ZHANG Zhen-wei,XIANYU Zhi-qun.The apoptotic pathway of breast cancer multidrug resistant cells[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(15):1475-1478.DOI:
The apoptotic pathway of breast cancer multidrug resistant cells
导致其线粒体功能下降的浓度,观察细胞形态学和线粒体超微结构的改变。应用DNA凝胶电泳、Annexin Ⅴ和PI双标记流式细胞术检测细胞凋亡发生,Rh123共聚焦显微镜检测线粒体膜电位和P-gp功能,Western blot检测细胞色素C(Cyto C)的释放状况。 结果 4 mmol/L H
2
O
2
引起MCF-7/Adr线粒体整体功能不可逆的进行性下降,线粒体空化,嵴肿胀。MCF-7/Adr凋亡率(96.52%)显著高于MCF-7/wt(18.57%,P<0.01)。凋亡DNA电泳仅见800、1 600 bp 2个分子片段。MCF-7/Adr线粒体数量较MCF-7/wt减少,MCF-7/Adr膜电位下降。4 mmol/L H
Objective To investigate the possible apoptotic pathway in breast cancer daunorubicin-resistant subline
MCF-7/Adr cell line. Methods Drug-resistance cell line MCF-7/Adr expressing functional P-gp and its wild type MCF-7/wt cell line were used for comparison. The concentration of hydrogen peroxide (H
2
O
2
) that may lead to loss of mitochondrial function was determined using MTT assay. The cell morphology and the mitochondrial ultrasr
ucture were observed by invert and transmission electron microscopy
respectively. The apoptosis of the two cell lines was determined with DNA gel electrophoresis and Annexin V and PI double-stained flow cytometry. Mitochondrial membrane potential (MMP) and the function of P-gp were assessed with rhodamine 123 (Rh123) staining intensity by confocal microscopy. The release of cytochrome C from mitochondria was observed by Western blotting. Results The mitochondrial function of MCF-7/Adr was irreversibly damaged at the concentration of 4 mmol/L H
2
O
2
. The mitochondria were vacuolated and their cristae were swollen. The percentage of MCF-7/Adr cell apoptosis was significantly higher than that of MCF-7/wt
96.52% and 18.57%
respectively (P0.01). Only 800 and 1 600 Da DNA fragmentation was seen. The number of mitochondria and membrane potential of MCF-7/Adr mitochondria decreased as compared with those of MCF-7/wt. H
2
O
2
at the concentration of 4 mmol/L induced release of cytochrome C from MCF-7/Adr mitochondria to cytoplasma
but little was detected in MCF-7/wt. Conclusion MCF-7/Adr cells expressing functional P-gp are more sensitive to H
2
O
2
-mediated mitochondrial apoptosis. It may attribute to the changes of mitochondrial structure and function in MCF-7/Adr cells. These may suggest that some way which may modify mitochondrial characteristics may be benificial to overcome the multidrug resistance related to P-gp.
Protective effect of equol on mitochondrial damage induced by high glucose and fat in osteoblasts
Protective effect of citrus flavone against acute hypoxia in cultured human intestinal smooth muscle cells and the mechanism
Cinobufacini-induced apoptosis in human neuroblastoma SH-SY5Y cells
Ultrasound irradiation microbubble verapamil reverses multidrug resistance of neuroblastoma cells in vitro
Comparative proteomic analysis on cerebral cortex mitochondria between ischemic and normal cerebral contex in rats
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