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DEK表达下调通过抑制胃癌SGC-7901细胞中NF-κB信号途径诱导细胞凋亡
引用本文:张彩凤,董良鹏,夏永华,郭晓鹤,张利利,周慧聪,张兰芳,李贞娟,韩宇.DEK表达下调通过抑制胃癌SGC-7901细胞中NF-κB信号途径诱导细胞凋亡[J].中国病理生理杂志,2015,31(7):1197-1202.
作者姓名:张彩凤  董良鹏  夏永华  郭晓鹤  张利利  周慧聪  张兰芳  李贞娟  韩宇
作者单位:1. 新乡医学院第一附属医院 消化内科, 河南 卫辉 453100;
2. 新乡医学院第一附属医院 普通外科, 河南 卫辉 453100;
3. 新乡医学院第一附属医院 皮肤科, 河南 卫辉 453100
基金项目:河南省教育厅科技攻关项目(No. 2009B320008);河南省卫生厅科技攻关项目(No. 200804055);新乡医学院科研培育基金(No. 2013QN128)
摘    要:目的:研究DEK表达下调对胃癌SGC-7901细胞凋亡的影响,并分析其与NF-κB信号途径及凋亡相关蛋白表达的关系。方法:将DEK siRNA和对照siRNA转染胃癌SGC-7901细胞,并将SGC-7901细胞分为未处理组、对照siRNA组及DEK siRNA组。采用实时荧光定量PCR和Western blot检测3组胃癌SGC-7901细胞中DEK mRNA和蛋白的表达;流式细胞术检测3组SGC-7901细胞凋亡的变化;Caspase-Glo-3/9试剂盒检测3组SGC-7901细胞中caspase-3和caspase-9的活性;Western blot技术检测3组SGC-7901细胞中NF-κB信号途径关键调控蛋白p65及凋亡相关蛋白Bcl-2和Bax的表达。结果:与未处理组和对照siRNA组相比,DEK siRNA组SGC-7901细胞中DEK的mRNA和蛋白表达水平显著下调(P0.05)。DEK siRNA组SGC-7901细胞的早期凋亡率和总凋亡率均显著高于未处理组和对照siRNA组(P0.05)。最为显著的是,DEK siRNA转染细胞后,p65和Bcl-2蛋白表达下调,Bax蛋白表达上调,并伴随caspase-3和caspase-9活性上升。结论:DEK表达下调介导的SGC-7901细胞凋亡可能与NF-κB信号途径密切相关。

关 键 词:胃癌  DEK  细胞凋亡  NF-κB信号途径  
收稿时间:2014-12-29

Downregulation of DEK induces cell apoptosis via inhibition of NF-κB signaling pathway in gastric carcinoma SGC-7901 cells
ZHANG Cai-feng,DONG Liang-peng,XIA Yong-hua,GUO Xiao-he,ZHANG Li-li,ZHOU Hui-cong,ZHANG Lan-fang,LI Zhen-juan,HAN Yu.Downregulation of DEK induces cell apoptosis via inhibition of NF-κB signaling pathway in gastric carcinoma SGC-7901 cells[J].Chinese Journal of Pathophysiology,2015,31(7):1197-1202.
Authors:ZHANG Cai-feng  DONG Liang-peng  XIA Yong-hua  GUO Xiao-he  ZHANG Li-li  ZHOU Hui-cong  ZHANG Lan-fang  LI Zhen-juan  HAN Yu
Institution:1. Department of Gastroenterology, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, China;
2. Department of General Surgery, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, China;
3. Department of Dermatology, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, China
Abstract:AIM: To investigate the effect of DEK downregulation on the apoptosis of gastric carcinoma SGC-7901 cells, and to explore its associations with NF-κB signaling pathway and apoptosis related proteins. METHODS: SGC-7901 cells with different treatments were divided into 3 groups including untreated group, control siRNA group and DEK siRNA group. The expression of DEK at mRNA and protein levels in the SGC-7901 cells was detected by real-time PCR and Western blot. The cell apoptosis was examined by flow cytometry. Furthermore, the activities of caspase-3 and caspase-9 in the SGC-7901 cells were investigated by Caspase-Glo®-3/9 kit. Finally, the expression of key regulatory protein p65 of NF-κB signaling pathway and apoptosis-related proteins Bcl-2 and Bax in the SGC-7901 cells was investigated by Western blot. RESULTS: Compared with untreated group and control siRNA group, the expression of DEK at mRNA and protein levels was significantly downregulated in DEK siRNA group (P<0.05). In addition, the ratios of early phase apoptosis and total apoptosis in DEK siRNA group were markedly higher than those in untreated group and control siRNA group (P<0.05). Most notably, the decrease in p65 and Bcl-2 proteins, increase in Bax protein and the increases of caspase-3 and caspase-9 activities were observed in DEK siRNA group. CONCLUSION: Downregulation of DEK mediates cell apoptosis of gastric carcinoma may be tightly associated with NF-κB signaling pathway.
Keywords:Gastric carcinoma  DEK  Apoptosis  NF-κB signaling pathway
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