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作 者:金灵莉[1] 杜勇[1] 杨艳果[1] 周春芳[1] 吕飞[1] 卢光新[1]
机构地区:[1]湖北医药学院附属人民医院消化内科,湖北十堰442000
出 处:《医学新知》2013年第5期336-338,共3页New Medicine
摘 要:目的探讨蛋白激酶B(Akt)抑制剂哌立福新对食管癌细胞侵袭的作用机制。方法应用哌立福新作用于人食管癌Ecal09细胞株,通过WesternBlotting检测Akt信号通路中相关蛋白Akt、基质金属蛋白-2(MMP-2)基质金属蛋白-9(MMP-2)的表达情况。通过Transwell实验评价食管癌Ecal09细胞侵袭变化情况。结果WesternBlotting结果示:与空白对照组、DMSO组相比,哌立福新组能有效抑制食管癌Ecal09细胞中Akt、MMP-2、MMP-9蛋白的表达。Transwell侵袭实验表明:DMSO组、空白对照组、哌立福新组穿过上室的平均细胞数分别为(81.3±1.52)、(81.0±2.65)、(44.6±2.52),三组的差异具有统计学意义(F=255.1,P〈0.05)。结论哌立福新能有效抑制食管癌Eeal09细胞Akt信号通路中相关蛋白的表达,在体外显著抑制Ecal09细胞的侵袭。Objective To investigate the effects of Akt inhibitor perifosine on migration of esophageal carcinoma cells. Methods Ecal09 cells were treated with perifosine. Expressions of Akt, MMP - 2 and MMP - 9 were detected with western blotting. The effects of perifosine on Ecal09 cell migration were evaluated by Transwell migration experi- ment. Results Perifosine had obvious inhibitory effects on Akt, MMP - 2 and MMP - 9 compared with blank group and DMSO group. Transwell migration experiment showed that average cell numbers through the house in three groups were ( 81.3 ± 1.52 ), ( 81.0± 2.65 ) and (44.6 ± 2.52 ). There were significant differences among three groups ( F = 255.1, P 〈 0.05 ). Conclusion Perifosine can inhibit the expression of related proteins in Akt signaling pathway in Ecal09 cells, and inhibit the migration of Ecal09 cells in vitro.
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