Effect of chemopreventive agents on glutathione S-transferase P1-1 gene expression mechanisms via activating protein 1 and nuclear factor kappaB inhibition
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.
机构:The Division of Infectious Diseases, Children's Hospital Research Foundation, Department of Pediatrics, University of Cincinnati College of Medicine, OH
机构:The Division of Infectious Diseases, Children's Hospital Research Foundation, Department of Pediatrics, University of Cincinnati College of Medicine, OH