Author/Authors :
Chen، نويسنده , , George G. and Chan، نويسنده , , Ursula P.F. and Bai، نويسنده , , Long-Chuan and Fung، نويسنده , , King Yip and Tessier، نويسنده , , Art and To، نويسنده , , Ann K.Y. and Merchant، نويسنده , , Juanita L. and Lai، نويسنده , , Paul B.S.، نويسنده ,
Abstract :
ZBP-89 inhibits the some tumor cells but its role in HCC is unknown. We investigated effect of ZBP-89 on cell death of 5 HCC cell lines with different status of p53. We found that ZBP-89 significantly induced cell death of all HCC cells particularly those with wild-type p53. The inhibition was well correlated with the induction of caspase-6 activity. The inhibition of caspase-6 abolished the effect of ZBP-89. ZBP-89 reduced the cells in G2-M but increased them in S phase. With the changes in caspase-6 and cell cycle, ZBP-89 greatly enhanced the killing effectiveness of 5-fluorouracil or staurosporine in HCC cells.
Keywords :
caspase-6 , cell cycle , hepatocellular carcinoma , p53 , Proliferation , ZBP-89