Nonomura N, Miki T, Yokoyama M, Imazu T, Takada T, Takeuchi S, Kanno N, Nishimura K, Kojima Y, Okuyama A
Department of Urology, Osaka University Medical School, 2-2 Yamada-oka, Suita, Osaka, 565, Japan.
Biochem Biophys Res Commun. 1996 Dec 24;229(3):945-51. doi: 10.1006/bbrc.1996.1906.
We have investigated the Fas-mediated apoptosis of cultured human renal cell carcinoma OUR-10. OUR-10 cells express Fas antigen on their cell surface and showed apoptotic cell death by stimulation with anti-Fas agonistic antibody. Cell proliferation of OUR-10 was reduced to 62% by the addition of anti-Fas antibody. The cytotoxic effect of anti-Fas antibody on OUR-10 was augmented by the pretreatment of these cells with interferon-gamma, not with interferon-alpha or with interleukin-2. Flow cytometry demonstrated that preculture of Our-10 cells with interferon-gamma increased the cell surface Fas antigen. Immunohistochemical analysis of resected tissues from the patients with renal cancer revealed stronger expression of Fas antigen on the surface of cancer cells than that of normal cells. These data suggest that Fas may be one of the possible targets for a novel approach to human kidney cancer, and the efficiency of this Fas-mediated treatment for kidney cancer could be augmented by the treatment with interferon-gamma.
我们研究了Fas介导的人肾癌细胞系OUR-10的凋亡情况。OUR-10细胞在其细胞表面表达Fas抗原,并且通过抗Fas激动性抗体刺激可出现凋亡性细胞死亡。加入抗Fas抗体后,OUR-10的细胞增殖减少至62%。用干扰素-γ预处理这些细胞可增强抗Fas抗体对OUR-10的细胞毒性作用,而干扰素-α或白细胞介素-2预处理则无此作用。流式细胞术表明,用干扰素-γ预培养Our-10细胞可增加细胞表面Fas抗原。对肾癌患者切除组织的免疫组化分析显示,癌细胞表面Fas抗原的表达强于正常细胞。这些数据表明,Fas可能是人类肾癌新治疗方法的可能靶点之一,并且用干扰素-γ治疗可增强这种Fas介导的肾癌治疗效果。