Green tea polyphenol (-)-epigallocatechin-3-gallate inhibits cyclooxygenase-2 expression in colon carcinogenesis

被引:113
作者
Peng, G
Dixon, DA
Muga, SJ
Smith, TJ
Wargovich, MJ
机构
[1] S Carolina Canc Ctr, Columbia, SC 29203 USA
[2] Univ S Carolina, Sch Med, Dept Pathol & Microbiol, Columbia, SC 29208 USA
[3] Univ S Carolina, Dept Biol Sci, Columbia, SC 29208 USA
[4] Univ S Carolina, Coll Pharm, Columbia, SC 29208 USA
关键词
EGCG; COX-2; gene expression; NF-kappa B; MAPKs; colon cancer cells;
D O I
10.1002/mc.20166
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tea, one of the most widely consumed beverages worldwide, has been shown to have anti-cancer activity in various cancers including colon cancer. It has been demonstrated that overexpression of the inducible isoform of cyclooxygenase (COX-2) occurs during colon tumorigenesis and inhibition of COX-2 by non-steroidal anti-inflammatory drugs (NSAIDs) is chemopreventive. To determine whether the anti-cancer effect associated with green tea impacted COX-2 expression levels, human colorectal cancer cell lines HT-29 and HCA-7, were treated with (-)-epigallocatechin-3-gallate (EGCG), the most abundant and effective polyphenol of green tea. EGCG significantly inhibited constitutive COX-2 mRNA and protein overexpression. The inhibitory effects of EGCG on signaling pathways controlling COX-2 expression were examined. We observed that EGCG downregulated the ERK1/2 and Akt pathways in colon cancer cells. The effect of EGCG on COX-2 expression resulted in decreased COX-2 promoter activity via inhibition of nuclear factor kappa B (NF-kappa B) activation. EGCG also promoted rapid mRNA decay mediated through the COX-2 3' untranslated region (3'UTR). In conclusion, these data suggest that inhibition of COX-2 is a mechanism for the anti-proliferative effect of green tea and emphasizes the role that dietary factors have as anti-cancer agents. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:309 / 319
页数:11
相关论文
共 47 条
[1]   Inhibition of ultraviolet B-mediated activation of nuclear factor κB in normal human epidermal keratinocytes by green tea Constituent (-)-epigallocatechin-3-gallate [J].
Afaq, F ;
Adhami, VM ;
Ahmad, N ;
Mukhtar, H .
ONCOGENE, 2003, 22 (07) :1035-1044
[2]   Green tea polyphenol epigallocatechin-3-gallate inhibits the IL-1β-induced activity and expression of cyclooxygenase-2 and nitric oxide synthase-2 in human chondrocytes [J].
Ahmed, S ;
Rahman, A ;
Hasnain, A ;
Lalonde, M ;
Goldberg, VM ;
Haqqi, TM .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (08) :1097-1105
[3]   Dietary catechins and cancer incidence among postmenopausal women: the Iowa Women's Health Study (United States) [J].
Arts, ICW ;
Jacobs Jr, DR ;
Gross, M ;
Harnack, LJ ;
Folsom, AR .
CANCER CAUSES & CONTROL, 2002, 13 (04) :373-382
[4]  
August DA, 1999, CANCER EPIDEM BIOMAR, V8, P709
[5]   Green tea and tea polyphenols in cancer prevention [J].
Chen, D ;
Daniel, KG ;
Kuhn, DJ ;
Kazi, A ;
Bhuiyan, M ;
Li, LH ;
Wang, ZG ;
Wan, SB ;
Lam, WH ;
Chan, TH ;
Dou, QP .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :2618-2631
[6]  
Chen LS, 1997, DRUG METAB DISPOS, V25, P1045
[7]  
CHO KR, 1992, CANCER, V70, P1727, DOI 10.1002/1097-0142(19920915)70:4+<1727::AID-CNCR2820701613>3.0.CO
[8]  
2-P
[9]   Mechanisms of inhibition of the Ras-MAP kinase signaling pathway in 30.7b Ras 12 cells by tea polyphenols (-)-epigallocatechin-3-gallate and theaflavin-3,3′-digallate [J].
Chung, JY ;
Park, JO ;
Phyu, H ;
Dong, ZG ;
Yang, CS .
FASEB JOURNAL, 2001, 15 (09) :2022-+
[10]  
De Lorenzo MS, 2003, CLIN CANCER RES, V9, P5036