Luk Sharon Chui-Wah, Siu Stephanie Wing-Fai, Lai Chun-Kit, Wu Ying-Jye, Pang Shiu-Fun
Technology Development, CK Life Sciences Int'l Inc., 2 Dai Fu Street, Tai Po Industrial Estate, Hong Kong, China.
Int J Med Sci. 2005;2(2):64-69. doi: 10.7150/ijms.2.64. Epub 2005 Apr 1.
CKBM is a natural product that exhibits a novel anti-tumor activity through the induction of cell cycle arrest and apoptosis. We have investigated its effects on cell cycle regulation using a gastric cancer cell line, AGS. The effects of CKBM on cell proliferation, cell cycle regulation and apoptosis were analyzed using BrdU (5-bromo-2'-deoxyuridine) cell proliferation assay and flow cytometric analysis, respectively. Specific cellular protein expressions were measured using Western blot analysis. Flow cytometric analysis indicated that CKBM induced G2/M cell cycle arrest and apoptosis, whereas differential protein expressions of p21, p53 and 14-3-3sigma (stratifin) using Western blot analysis were enhanced. The differential expressions of p21, p53 and 14-3-3sigma in AGS cancer cells after CKBM treatment may play critical roles in the G2/M cell cycle arrest that blocks cell proliferation and induces apoptosis.
CKBM是一种天然产物,通过诱导细胞周期停滞和凋亡表现出新型抗肿瘤活性。我们使用胃癌细胞系AGS研究了其对细胞周期调控的影响。分别采用BrdU(5-溴-2'-脱氧尿苷)细胞增殖试验和流式细胞术分析,分析了CKBM对细胞增殖、细胞周期调控和凋亡的影响。使用蛋白质免疫印迹分析测量特定细胞蛋白表达。流式细胞术分析表明,CKBM诱导G2/M期细胞周期停滞和凋亡,而蛋白质免疫印迹分析显示p21、p53和14-3-3sigma(层粘连蛋白)的差异蛋白表达增强。CKBM处理后AGS癌细胞中p21、p53和14-3-3sigma的差异表达可能在阻止细胞增殖并诱导凋亡的G2/M期细胞周期停滞中起关键作用。