Yu R, Jiao J J, Duh J L, Gudehithlu K, Tan T H, Kong A N
Department of Pharmaceutics and Pharmacodynamics, College of Pharmacy, University of Illinois, Chicago 60612, USA.
Carcinogenesis. 1997 Feb;18(2):451-6. doi: 10.1093/carcin/18.2.451.
Green tea polyphenols, major constituents of green tea, are potent chemopreventive agents in a number of experimental models of cancer in animals. The mechanisms of cancer protection by these agents are not clear, but may involve modulation of the enzyme systems responsible for the detoxification of chemical carcinogens. The present studies show that a green tea polyphenol extract (GTP) induces chloramphenicol acetyltransferase (CAT) activity in human heptoma HepG2 cells transfected with a plasmid construct which contains an antioxidant-responsive element (ARE) and a minimal glutathione S-transferase Ya promoter linked to the CAT reporter gene. This indicates that GTP stimulates the transcription of Phase II detoxifying enzymes through the ARE. To explore the upstream signaling pathways leading to gene expression, we studied the involvement of the mitogen-activated protein kinases (MAPKs) extracellular signal-regulated kinase 2 (ERK2) and c-Jun N-terminal kinase 1 (JNK1). Potent activation of ERK2 was seen following treatment of HepG2 cells with different concentrations of GTP. Similar to ERK2, JNK1 was also strongly activated by treatment with GTP, although to a lesser extent and in a different dose-dependent fashion. Kinetic studies revealed that GTP activation of JNK1 was delayed and sustained, whereas ERK2 activation was rapid and transient. Furthermore, GTP treatment also increased mRNA levels of the immediate-early genes c-jun and c-fos, as determined by reverse transcriptase-coupled polymerase chain reaction. Taken together, these studies provide insights into the action of GTP and suggest that the stimulation MAPKs may be the potential signaling pathways utilized by GTP to activate ARE-dependent genes.
绿茶多酚是绿茶的主要成分,在多种动物癌症实验模型中是有效的化学预防剂。这些药剂预防癌症的机制尚不清楚,但可能涉及对负责化学致癌物解毒的酶系统的调节。目前的研究表明,一种绿茶多酚提取物(GTP)在转染了含有抗氧化反应元件(ARE)和与氯霉素乙酰转移酶(CAT)报告基因相连的最小谷胱甘肽S-转移酶Ya启动子的质粒构建体的人肝癌HepG2细胞中诱导CAT活性。这表明GTP通过ARE刺激II期解毒酶的转录。为了探索导致基因表达的上游信号通路,我们研究了丝裂原活化蛋白激酶(MAPK)细胞外信号调节激酶2(ERK2)和c-Jun氨基末端激酶1(JNK1)的参与情况。用不同浓度的GTP处理HepG2细胞后,观察到ERK2有强力激活。与ERK2类似,JNK1也被GTP处理强烈激活,尽管程度较小且呈不同的剂量依赖性方式。动力学研究表明,GTP对JNK1的激活是延迟且持续的,而ERK2的激活是快速且短暂的。此外,通过逆转录聚合酶链反应测定,GTP处理还增加了即早基因c-jun和c-fos的mRNA水平。综上所述,这些研究为GTP的作用提供了见解,并表明MAPKs的刺激可能是GTP用于激活ARE依赖性基因的潜在信号通路。