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作 者:杨彩玲[1] 张景航[2] 任铭新[3] 张应花[3] 崔卫刚[3]
机构地区:[1]新乡医学院第一附属医院口腔外科,卫辉453100 [2]新乡医学院病理科,新乡453003 [3]新乡医学院人体解剖学教研室,新乡453003
出 处:《郑州大学学报(医学版)》2014年第5期681-683,共3页Journal of Zhengzhou University(Medical Sciences)
摘 要:目的:研究埃克替尼对涎腺腺样囊性癌细胞系ACC-M细胞凋亡的影响及可能机制。方法:ACC-M细胞分为6组,即对照组,低、中、高剂量(10、20、40μmol/L)埃克替尼组,MnTMPyP组以及MnTMPyP+埃克替尼组。采用MTT法检测各组细胞的活性,Caspase-3活力检测试剂盒检测Caspase-3蛋白的活力,DCFH-DA荧光探针检测ROS水平,Western blot检测线粒体和胞质MnSOD蛋白的表达。结果:与对照组相比,埃克替尼低、中、高剂量组细胞活性降低,Caspase-3蛋白活力增强,ROS水平升高,线粒体中MnSOD蛋白表达减少,胞质中MnSOD蛋白表达增加(P均<0.05);MnTMPyP能拮抗上述变化(P均<0.05)。结论:埃克替尼可能通过ROS介导的MnSOD线粒体转位诱导ACC-M细胞凋亡。Aim:To observe the effect and mechanism of icotinib on the apoptosis induction of the salivary adenoid cystic carcinoma-M( ACC-M) cells.Methods:ACC-M cells were allocated into control group ,low-,median-,high-concen-tration(10,20,40 μmol/L) icotinib-treatment groups,MnTMPyP group and MnTMPyP +icotinib group.The cell viability of ACC-M was measured by MTT assay .The expression of Caspase-3 was assessed by Caspase-3 activity detection kit .The lev-el of ROS was assayed by the fluorescent probe using DCFH-DA.The expression of MnSOD in mitochondrion was deter-mined by Western blot analysis .Results:Compared with control group ,the cell viability of ACC-M significantly decreased in low-,median-,high-concentration icotinib groups ,the expressions of Caspase-3 and ROS increased ,the expression of Mn-SOD significantly decreased in mitochondrion while increased in cytoplasm (all P〈0.05).However,MnTMPyP reversed the effects of icotinib(all P〈0.05).Conclusion:Icotinib may induce apoptosis of ACC-M cells through ROS-mediated Mn-SOD mitochondrial translocation .
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