Effect of chemopreventive agents on glutathione S-transferase P1-1 gene expression mechanisms via activating protein 1 and nuclear factor kappaB inhibition

被引:62
作者
Duvoix, A
Delhalle, S
Blasius, R
Schnekenburger, M
Morceau, F
Fougère, M
Henry, E
Galteau, MM
Dicato, M
Diederich, M
机构
[1] Hop Kirchberg, Lab Biol Mol & Cellulaire Canc, L-2540 Luxembourg, Luxembourg
[2] Fac Pharm Nancy, F-54000 Nancy, France
关键词
GSTP1-1; chemopreventive agents; carcinogenesis; drug resistance; leukemia;
D O I
10.1016/j.bcp.2004.05.032
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glutathione S-transferase P1-1 (GSTP1-1) is a phase II drug metabolism enzyme implicated in carcinogenesis and development of resistance to anti-cancer drugs. It was previously shown that both activating protein 1 (AP-1) and nuclear factor kappaB (NF-kappaB) are involved in its regulation. In the present study we examined the inhibitory effect of several chemopreventive agents on the tumor necrosis factor (TNF) alpha- or 12-O-tetradecanoylphorbol 13 acetate (TPA)-induced promoter activity of GSTP1-1, as demonstrated by transient transfection experiments in K562 and U937 leukemia cells. Our results provide evidence for a differential effect of chemopreventive agents such as beta-lapachone, emodin, sanguinarine and capsaicin, which significantly inhibit reporter gene expression as well as TNFalpha- and TPA-induced binding of AP-1 and NF-kappaB, whereas trans-anethole and silymarin do not produce any inhibitory effect. Our results demonstrate the ability of selected chemopreventive agents to decrease GSTP1-1 gene expression mechanisms and could thus contribute to reduce the incidence of glutathione related drug resistance in human leukemia. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1101 / 1111
页数:11
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