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肿瘤坏死因子相关细胞凋亡诱导配体受体-4在人胰腺癌组织中的表达
引用本文:廖泉,郭俊超,赵玉沛.肿瘤坏死因子相关细胞凋亡诱导配体受体-4在人胰腺癌组织中的表达[J].中国普外基础与临床杂志,2003,10(6):535-538.
作者姓名:廖泉  郭俊超  赵玉沛
作者单位:中国医学科学院中国协和医科大学北京协和医院外科,北京,100730
摘    要:目的:通过检测肿瘤坏死因子相关细胞凋亡诱导配体受体-4(TRAIL-R4)在胰腺癌组织中的表达,探讨胰腺癌细胞抵抗细胞凋亡的机理。方法:应用mRNA印迹法(Northern blotting)、蛋白质印迹法(Western blotting)和免疫组织化学技术,定性、定位分析TRAIL-R4在正常胰腺组织和胰腺癌组织中的表达。结果:TRAIL-R4 mRNA和蛋白在正常胰腺组织中呈弱表达或不表达,而在胰腺癌组织中呈高表达;免疫组织化学检测显示,在胰腺癌细胞中TRAIL-R4蛋白呈强染色。结论:TRAIL-R4表达水平在正常胰腺组织与胰腺癌组织中存在显著差异,提示胰腺癌细胞中可能存在对TRAIL介导的细胞凋亡抵抗新机理。

关 键 词:肿瘤坏死因子  细胞凋亡  诱导  配体  胰腺癌  表达  癌组织
文章编号:1007-9424(2003)06-0535-04
修稿时间:2003年6月5日

Expression of Tumor Necrosis Factor Related Apoptosis Inducing Ligand Receptor-4 in Human Pancreatic Cancer
LIAO Q uan,GUO J un-chao,ZHAO Y u-pei.Expression of Tumor Necrosis Factor Related Apoptosis Inducing Ligand Receptor-4 in Human Pancreatic Cancer[J].Chinese Journal of Bases and Clinics In General Surgery,2003,10(6):535-538.
Authors:LIAO Q uan  GUO J un-chao  ZHAO Y u-pei
Institution:LIAO Q uan,GUO J un-chao,ZHAO Y u-pei. Department of General Surgery,Peking Union Medical College Hospital,Beijing 100730,China
Abstract:Objective To investigate the mechanism of the resistance of pancreatic cancer cells to tumor necrosis factor related apoptosis inducing ligand (TRAIL)-mediated apoptosis. Methods The expression of TRAIL receptor-4 (TRAIL-R4) in normal pancreas tissue and pancreatic cancer was analyzed by using Northern blotting, Western blotting and immunohistochemistry. Results TRAIL-R4 mRNA and protein were expressed at moderate to high levels in human pancreatic cancer, but demonstrated weak to negative in the normal pancreas. Moreover, pancreatic cancer cells showed strong TRAIL-R4 immunostaining throughout the tumor mass. Conclusion TRAIL-R4 levels are significantly different in pancreatic cancer in comparison to the normal pancreas. These findings give new insights into the resistance mechanisms of pancreatic cancer cells towards TRAIL-mediated apoptosis.
Keywords:Pancreatic cancer Tumor necrosis factor related apoptosis inducing ligand receptor-4 Cell apoptosis
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