Kase S, Osaki M, Honjo S, Takeda A, Adachi K, Araki K, Ito H
Dept of Microbiology and Pathology, Faculty of Medicine, Tottori University, Yonago, Japan.
J Exp Clin Cancer Res. 2004 Jun;23(2):301-7.
It is well known that cyclooxygenase (COX) -2 is expressed in a variety of human malignant solid tumors, associated with tumor angiogenesis, cell proliferation and inhibition of apoptosis. Here, we examined the effect of NS398, a selective COX-2 inhibitor, on two human esophageal squamous cell carcinoma (SCC) cell lines, TE-1 and TE-12. Western blot analysis confirmed the expression of COX-2 in TE-12, but not in TE-1. Treatment with 100microM NS398 suppressed the cell viability in TE-12 (48.6% of control) after 48 hours, in contrast to showing no effects in TE-1. The apoptotic index was extremely low in both cell lines after the treatment. NS398 clearly increased the number of cells in the G2/M phase and decreased the cells in the G1 and S phases in TE-12, but not TE-1. A pre-G1 fraction was not noted in either cell line. Moreover, TE-12 cells showed a decrease in the expression levels of cyclin B1 and an increase in p27Kip1. These findings suggest that NS398 inhibits cell growth and induces G2/M arrest in human SCC cells expressing COX-2.
众所周知,环氧化酶(COX)-2在多种人类恶性实体瘤中表达,与肿瘤血管生成、细胞增殖及细胞凋亡抑制相关。在此,我们检测了选择性COX-2抑制剂NS398对两种人食管鳞状细胞癌(SCC)细胞系TE-1和TE-12的作用。蛋白质免疫印迹分析证实COX-2在TE-12中表达,但在TE-1中不表达。用100微摩尔NS398处理48小时后,TE-12中的细胞活力受到抑制(为对照的48.6%),相比之下,TE-1中未显示出作用。处理后两种细胞系中的凋亡指数均极低。NS398明显增加了TE-12中G2/M期的细胞数量,并减少了G1期和S期的细胞数量,但对TE-1无此作用。两种细胞系中均未观察到前G1期细胞比例。此外,TE-12细胞中细胞周期蛋白B1的表达水平降低,p27Kip1增加。这些发现表明,NS398抑制表达COX-2的人SCC细胞的生长并诱导G2/M期阻滞。