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机构地区:[1]中国医科大学附属第一医院肿瘤研究所二室,辽宁沈阳110001
出 处:《中国血液流变学杂志》2011年第2期222-226,共5页Chinese Journal of Hemorheology
摘 要:目的研究TRAIL联合白藜芦醇(Res)对乳腺癌MDA-MB-231细胞DR和caspase表达的影响。方法MTT法检测细胞增殖;流式细胞术检测细胞凋亡及细胞表面DR4、DR5蛋白的表达;分光光度法检测caspase-3、caspase-8相对活性;荧光定量PCR检测DR4、DR5及caspase-3、caspase-8 mRNA的表达。结果50μmol/L和100μmo/L,Res分别与50ng/mL TRAIL联合作用后,对MDA-MB-231细胞增殖的抑制率及细胞凋亡率分别与单独应用相应浓度的Res和TRAIL比较,均存在显著差异(P〈0.01)。50μmol/L和100μmol/LRes分别与50ng/mLT RAIL联合作用后,caspase-3、caspase-8的相对活性与对照组及单用TRAIL、Res比较均明显增强,差异显著(P〈0.01)。Res作用后,细胞表面DR4、DR5荧光指数与对照组比较明显增强。荧光定量PCR结果显示与对照组比较.Res作用后DR4、DR5mRNA表达上调;与单独用药比较,TRAIL联合Resetcagpase-3、easpase-8 mRNA表达上调。结论TRAIL和Res联合应用对诱导乳腺癌MDA-MB-231细胞凋亡具有明显的协同效果,其作用机制可能与增加DR和caspase活性有关。Objective To explore the mechanism of TRAIL combined with resveratrol inducing apoptosis in MDA-MB-231 breast cancer cell line. Methods The proliferation was detected by MTT assay.Apoptosis of cells and the expression of DR4 and DR5 on the surface of MDA-MB-231 cell were examined by flow cytometry. The relative activity of caspase-3 and caspase-8 were examined by spectrophotometric method.The expression of DR4,DR5,caspase-3 and caspase-8 mRNA were measured by Real time reverse transcription-polymerase chain reaction(Real time PCR).Results After cells were exposed to 50ng/mL TRAIL combined with 50 μmol/L,100 μmol/L resveratrol for 12h,the inhibitory rate and the apoptotic percentage were increased markedly(P 〈 0.01).After cells were exposed to 50ng/mL TRAIL combined with 50 μmol/L,100 μmol/L resveratrol for 12h,the relative activities of caspase-3 and caspase-8 were advanced(P 〈 0.01).Compared with control group and one treatment factor, the fluorescence index of DR4 and DR5 on the surface of cells were increased (P 〈 0.05). And the expression of DR4,DR5,caspase-3 and caspase-8 mRNA were enhanced markedly(P 〈 0.0 l).Conelusion TRAIL and resveratrol are able to kill breast cancer MDA-MB-231 cell,respectively, while TRAIL with resveratrol together applied can have synergistic effect on MDA-MB-231 cell by increasing the DR and caspase activities.
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