Reactive oxygen species-mediated induction of apoptosis by a plant alkaloid 6-methoxydihydrosanguinarine in HepG2 cells

被引:40
|
作者
Yin, HQ
Kim, YH
Moon, CK
Lee, BH
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[2] Wonkwang Univ, Med Resources Res Ctr, Jeonbuk 570749, South Korea
[3] Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea
关键词
6-methoxydihydrosanguinarine (6WE); apoptosis; reactive oxygen species (ROS); p53/bax; cytochrome c; antioxidant; HepG2;
D O I
10.1016/j.bcp.2005.04.020
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have found in the previous study that 6-methoxydihydrosanguinarine (6ME). a henzophenarithridine alkaloid isolated from Hylomecon species, may have potential as a chemotherapeutic agent. However, the mechanisms of 6ME-induced cell death have not been investigated. The purpose of the present study was to determine the apoptosis-inducing potential of 6ME in human hepatocarcinoma HepG2 cells and the role of reactive oxygen species in 6ME-induced apoptosis, It can be concluded from the results that 6ME inhibits the growth of HepG2 cells in a concentration- and time-dependent manner (IC50=3.8 +/- 0.2 mu M following 6 h incubation). Treatment of HepG2 cells with 6ME resulted in the release of mitochondrial cytochrome c followed by the activation of caspase proteases, and subsequent proteolytic cleavage of poly(ADP-ribose) polymerase. 6ME increased the expression of p53 and bax and decreased the expression of bcl-2. The cytotoxic effect of 6ME is mediated by the time-dependent generation of reactive oxygen species. Our results also show that preincubation of HepG2 cells with vitamin C decreased the expression of p53 and bax and inhibited the release of cytochrome c, activation of downstream caspase and the cleavage of poly(ADP-ribose) polymerase. thus inhibiting the apoptosis inducing effect of 6ME. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:242 / 248
页数:7
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