Activation of signal transduction kinases by tamoxifen

被引:33
|
作者
Duh, JL
Yu, R
Jiao, JJ
Matwyshyn, GA
Li, W
Tan, TH
Kong, ANT
机构
[1] UNIV ILLINOIS,COLL PHARM,CTR PHARMACEUT BIOTECHNOL,DEPT PHARMACEUT & PHAMACODYNAM,CHICAGO,IL 60607
[2] UNIV CHICAGO,BEN MAY INST,CHICAGO,IL 60637
[3] BAYLOR COLL MED,DEPT MICROBIOL & IMMUNOL,HOUSTON,TX 77030
关键词
tamoxifen; MAP kinases; MAPK; JNK; ERK; AP-1; ARE; NF-kappa B; signal transduction;
D O I
10.1023/A:1012048626963
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose, To study the signal transduction mechanisms of tamoxifen via the activation of MAPKs, JNK and ERK in order to understand its regulation of gene expression. Methods. The effects of tamoxifen (TAM) on the activation of serine/threonine mitogen-activated protein kinase (MAPK, p42/ERK2) and the stress-activated protein kinases (p46 SAPK or c-Jun N-terminal kinase, JNK1) were evaluated using a human cervical epitheloid carcinoma HeLa cell line. Results, TAM activated both JNK1 and ERK2 activities in a time- and dose-dependent manner in HeLa cells. The activation of JNK1 was enhanced when the cells were pretreated with prooxidant H2O2. Conclusions. These studies show that TAM activates the signal transduction kinases, JNK1 and ERK2, which may play important roles in the regulation of gene expression by TAM.
引用
收藏
页码:186 / 189
页数:4
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