To Ann K Y, Chen George G, Chan Ursula P F, Ye Caiguo, Yun Jing P, Ho Rocky L K, Tessier Art, Merchant Juanita L, Lai Paul B S
Department of Surgery, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong.
Biochim Biophys Acta. 2011 Jan;1813(1):222-30. doi: 10.1016/j.bbamcr.2010.09.005. Epub 2010 Sep 17.
ZBP-89 can enhance tumor cells to death stimuli. However, the molecular mechanism leading to the inhibitory effect of ZBP-89 is unknown. In this study, 4 liver cell lines were used to screen for the target of ZBP-89 on cell death pathway. The identified Bak was further analyzed for its role in ZBP-89-mediated apoptosis. The result showed that ZBP-89 significantly and time-dependently induced apoptosis. It significantly upregulated the level of pro-apoptotic Bak. ZBP-89 targeted a region between -457 and -407 of human Bak promoter to stimulate Bak expression based on the findings of Bak promoter luciferase report gene assay and electrophoretic mobility shift assay. ZBP-89-induced Bak increase and ZBP-89-mediated apoptosis were markedly suppressed by Bak siRNA, confirming that Bak was specifically targeted by ZBP-89 to facilitate apoptosis. In conclusion, this study demonstrated that ZBP-89 significantly induced apoptosis of HCC cells via promoting Bak level.
ZBP - 89可增强肿瘤细胞对死亡刺激的反应。然而,导致ZBP - 89产生抑制作用的分子机制尚不清楚。在本研究中,使用4种肝癌细胞系来筛选ZBP - 89在细胞死亡途径上的靶点。对鉴定出的Bak在ZBP - 89介导的凋亡中的作用进行了进一步分析。结果表明,ZBP - 89显著且呈时间依赖性地诱导凋亡。它显著上调促凋亡蛋白Bak的水平。基于Bak启动子荧光素酶报告基因检测和电泳迁移率变动分析的结果,ZBP - 89靶向人Bak启动子- 457至- 407区域以刺激Bak表达。Bak小干扰RNA显著抑制ZBP - 89诱导的Bak增加和ZBP - 89介导的凋亡,证实Bak是ZBP - 89促进凋亡的特异性靶点。总之,本研究表明ZBP - 89通过提高Bak水平显著诱导肝癌细胞凋亡。