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作 者:马会敏[1] 金国平[1] 王献伟[1] 单杰[1]
机构地区:[1]郑州大学基础医学院生物化学与分子生物学教研室,河南郑州450001
出 处:《河南医学研究》2007年第2期118-120,共3页Henan Medical Research
基 金:河南省科委资助项目(054022700);郑州市科委资助项目(05SGYS33211)
摘 要:目的:检测三氧化二砷(As2O3)诱导食管癌EC9706细胞凋亡过程中血红素加氧酶-1(HO-1)基因的表达,探讨HO-1的表达与化疗药物诱导肿瘤细胞凋亡的内在联系。方法:以食管癌EC9706细胞系作为研究模型,3μmol/L AS2O3作用于EC9706细胞,镜下观察细胞形态变化;MTT法绘制细胞生长曲线;以RT-PCR方法检测HO-1mRNA的表达。结果:As2O3作用于EC9706细胞4 h即可检测到HO-1基因表达升高,12 h表达水平升至最高,24 h回落到正常水平。结论:As203诱导EC9706细胞凋亡过程中,HO-1基因表达升高,呈时间依赖性变化,可能起到短暂的对抗氧化应激作用。Objective: To detect the expression of HO-1 gene in the apoptotic process of EC9706 cell induced by As2O3,and to approach the relationship between the expression of HO-1 gene and the tumor cell apoptosis induced by chemotherapeutics. Methods : EC9706 cell were treated with 3μmol/L As2O3 ,then to observe the change of cell' s appearance under microscope and record the cell growth curve using MTT method as well as detecting the expression of HO-1 mRNA with RTPCR method. Results: 4 h after cells were treated with As2O3 ,the expression of HO-1 mRNA had begin to rise . It reached the highest level at 12 h,and at 24 h,it had return to the normal level. Conclusion: In the apoptotic process of EC9706 cell induced by As2O3, the expression of HO-1 gene rises along with the time . The change may contribute to protecting tumor cells from oxidative stress temporarily.
关 键 词:食管癌EC9706细胞 血红素加氧酶-1 基因表达 三氧化二砷诱导凋亡
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