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三黄煎剂调节Aurora激酶A促进乳腺癌细胞凋亡的实验研究
作者姓名:许岩磊  陈曦琰  陈绪  卞卫和  姚昶  朱小纾  陈佳静
作者单位:1.南京中医药大学附属医院,江苏 南京?210029
摘    要:目的?探讨三黄煎剂对乳腺癌MCF-7、MDA-MB-231细胞凋亡的影响及Aurora激酶A(Aurora A)蛋白表达及功能的影响,并探讨其内在机制。方法?采用CCK-8法检测三黄煎剂对乳腺癌细胞MCF-7、MDA-MB-231增殖的影响。AnnexinV-FITC/PI法检测MCF-7、MDA-MB-231细胞凋亡率。q-PCR法检测MCF-7、MDA-MB-231细胞Aurora A、p53的mRNA表达水平。Western Blot法检测MCF-7、MDA-MB-231细胞凋亡相关蛋白的表达及Aurora A蛋白的表达。结果?三黄煎剂对MCF-7、MDA-MB-231细胞增殖抑制率呈浓度梯度依赖增长(P<0.05),给药48?h疗效好于24?h(P<0.05),与给药72?h无统计学差异(P>0.05)。三黄煎剂能够诱导MCF-7、MDA-MB-231细胞凋亡,并上调c-PARP、c-Caspase 3、Bax蛋白的表达,下调Bcl-2蛋白的表达,呈浓度梯度依赖。三黄煎剂能够下调Aurora A蛋白及mRNA的表达、上调p53蛋白及mRNA的表达。结论?三黄煎剂能够通过下调Aurora A蛋白及mRNA的表达,抑制Aurora A的生物活性,抑制MCF-7、MDA-MB-231细胞增殖,诱导其凋亡。 

关 键 词:三黄煎剂    Aurora  A    乳腺癌细胞    凋亡
收稿时间:5/3/2015 12:00:00 AM
修稿时间:2015/8/11 0:00:00

San Huang Decoction Promotes Apoptosis of Breast Cancer Cells Through Regulating Aurora Kinase A
Authors:XU Yan-lei  CHEN Xi-yan  CHEN Xu  BIAN Wei-he  YAO Chang  ZHU Xiao-shu  CHEN Jia-jing
Institution:1.The Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, China2.The School of Science and Health, The University of West Sydney, 2750, Australia
Abstract:OBJECTIVE?To explore the effect of San Huang decoction on the apoptosis of breast cancer cells and the effect on the mRNA and protein expression and function of Aurora kinase A and discuss the underlying mechanism of San Huang induced apoptosis. METHODS?The inhibition of breast cancer cells proliferation was determined by CCK-8 assay. The apoptosis of breast cancer cells was detected by AnnexinV-FITC/PI Staining. The expression of mRNA of Aurora A was examined by q-PCR analysis. The expression of apoptosis-related proteins and Aurora A were determined by Western Blot analysis. RESULTS?San Huang decoction inhibited the proliferation of breast cancer cells in a does-dependent manner(P<0.05). The effect of inhibition caused by San Huang decoction 48 hours after delivering to breast cancer cells was better than 24 hours(P<0.05) , although similar as 72 hours(P>0.05). San Huang decoction was also found to induce apoptosis in both MCF-7 and MDA-MB-231 cell lines in a dose-dependent manner. Consistent with cellular results, San Huang decoction treatment significantly increased the apoptosis-related protein level of cleaved-PARP(c-PARP), cleaved-Caspase 3(c-Caspase 3) and Bax, down-regulated Bcl-2 in a does-dependent manner. Meanwhile, San Huang decoction decreased the mRNA and protein level of Aurora A and increased those of p53 in a does-dependent manner. CONCLUSION?San Huang decoction at the first time was able to promote the apoptosis of breast cancer cells via inducing the suppression of Aurora A. 
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