Adachi Keiko, Osaki Mitsuhiko, Kase Satoru, Takeda Ami, Ito Hisao
Division of Organ Pathology, Department of Microbiology and Pathology, Faculty of Medicine, Tottori University, 86 Nishi-cho, Yonago, Tottori 683-8503, Japan.
Int J Oncol. 2003 Sep;23(3):713-9.
The Fas-Fas ligand system is one of the factors involved in cell death signaling. Aberrations in the signaling pathways leading to Fas-mediated apoptosis in tumor cells have been reported in a variety of human malignant tumors. However, the Fas-mediated apoptotic pathway has not been sufficiently elucidated in human gastric carcinomas. We examined the apoptotic pathway induced by anti-Fas antibody using seven human gastric carcinoma cell lines. Apoptosis was induced in a delayed fashion and the apoptotic indices (AI) after 48 h were approximately 30-40% in MKN-45 and KATO-III cells, which both showed cleavage of the Bid protein and release of Cytochrome c from the mitochondria. Our data also demonstrated no significant relationship between the expressions of various apoptosis-related proteins and the sensitivity or resistance to anti-Fas antibody-induced apoptosis, as far as we examined. Furthermore, the apoptosis signal was inhibited by treatment with Caspase-9 and -3 inhibitors in MKN-45 and KATO-III. These findings suggest that anti-Fas antibody induced apoptosis through the type II signaling pathway in the human gastric carcinoma cell lines, MKN-45 and KATO-III.
Fas-Fas配体系统是参与细胞死亡信号传导的因素之一。在多种人类恶性肿瘤中,均已报道了导致肿瘤细胞中Fas介导的细胞凋亡的信号通路异常。然而,Fas介导的凋亡途径在人类胃癌中尚未得到充分阐明。我们使用七种人类胃癌细胞系研究了抗Fas抗体诱导的凋亡途径。凋亡以延迟方式诱导,48小时后的凋亡指数(AI)在MKN-45和KATO-III细胞中约为30-40%,这两种细胞均显示Bid蛋白的裂解以及细胞色素c从线粒体的释放。就我们所检测的而言,我们的数据还表明各种凋亡相关蛋白的表达与抗Fas抗体诱导的凋亡的敏感性或抗性之间没有显著关系。此外,在MKN-45和KATO-III中,用Caspase-9和-3抑制剂处理可抑制凋亡信号。这些发现表明,抗Fas抗体通过II型信号通路在人类胃癌细胞系MKN-45和KATO-III中诱导凋亡。