(-)-EPIGALLOCATECHIN-3-GALLATE IN CAMELLIA-SINENSIS LEAVES FROM HIMALAYAN REGION OF SIKKIM - INHIBITORY EFFECTS AGAINST BIOCHEMICAL EVENTS AND TUMOR INITIATION IN SENCAR MOUSE SKIN

被引:73
作者
KATIYAR, SK [1 ]
AGARWAL, R [1 ]
WANG, ZY [1 ]
BHATIA, AK [1 ]
MUKHTAR, H [1 ]
机构
[1] DEPT VET AFFAIRS MED CTR,10701 EAST BLVD,CLEVELAND,OH 44106
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 1992年 / 18卷 / 01期
关键词
D O I
10.1080/01635589209514207
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently, we and others showed that the components of green tea may be useful cancer chemopreventive agents. It has been suggested that (-)-epigallocatechin-3-gallate (EGCG), the major constituent in green tea, may possess antitumor-promoting and/or anticarcinogenic effects in rodent tumor bioassay systems. During the chemical analysis of various green tea products, we found a traditionally preserved preparation of green tea used by tribes in the Himalayan region of Sikkim, India that was rich in EGCG. EGCG was isolated from this tea product, and its inhibitory effects were evaluated against the binding of topically applied H-3-labeled polycyclic aromatic hydrocarbons (PAHs) to epidermal DNA and 12-O-tetradecanoylphorbol-13-acetate (TPA) caused induction of epidermal ornithine decarboxylase (ODC) activity in Sencar mice, the short-term markers of tumor initiation and tumor promotion, respectively. Preapplication of EGCG resulted in significant inhibition (p < 0.05) in the binding of [H-3]PAH to epidermal DNA. Similarly, the topical application of EGCG resulted in significant inhibition (p < 0.005) in TPA-caused induction of epidermal ODC activity. In further studies, we assessed the anti-skin tumor-initiating effect of EGCG in Sencar mice in an initiation-promotion protocol. The application of EGCG before challenge with 7,12-dimethylbenz[a]anthracene as tumor initiator resulted in significant reduction both in percentage of mice with tumors and number of tumors per mouse compared with a non-EGCG-pretreated group of animals. The results of the present study suggest that the green tea preparation from Sikkim may be a good source for the isolation of EGCG and that this compound may have significant potential as a cancer chemopreventive agent.
引用
收藏
页码:73 / 83
页数:11
相关论文
共 41 条
[1]  
Stich H.F., The Beneficial and Hazardous Effects of Simple Phenolic Compounds, Mutat Res, 259, pp. 307-324, (1991)
[2]  
Mukhtar H., Athar M., Dietary Anticarcinogens and Cancer Prevention, Clev Clin J Med, 55, pp. 507-508, (1988)
[3]  
Wattenberg L.W., Inhibition of Carcinogenesis by Naturally Occurring and Synthetic Compounds, Antimutagenesis and Anticarcinogenesis. Mechanisms, 11, pp. 155-166, (1990)
[4]  
Mukhtar H., Das M., Bickers D.R., Inhibition of 3-Methylcholanthrene-Induced Skin Tumorigenicity in Balb/C Mice by Chronic Oral Feeding of Trace Amounts of Ellagic Acid in Drinking Water, Cancer Res, 46, pp. 2262-2265, (1986)
[5]  
Mukhtar H., Das M., Khan W.A., Wang Z.Y., Bik D.P., Et al., Exceptional Activity of Tannic Acid Among Naturally Occurring Plant Phenols in Protecting Against 7, 12-Dimethylbenz[a]anthracene— Benzo[a]pyrene—, 3-Methylcholanthrene and N-Methyl-N-Nitrosourea-Induced Skin Tumorigenesis in Mice, Cancer Res, 48, pp. 2361-2365, (1988)
[6]  
Athar M., Khan W.A., Mukhtar M., Effect of Dietary Tannic Acid on Epidermal, Lung and Forestomach Polycyclic Aromatic Hydrocarbon Metabolism and Tumorigenicity in SENCAR Mice, Cancer Res, 49, pp. 5784-5788, (1989)
[7]  
Wang Z.Y., Agarwal R., Zhou Z.C., Bickers D.R., Mukhtar H., Inhibition of Mutagenicity in Salmonella typhimurium and Skin Tumor Initiating and Tumor Promoting Activities in Sencar Mice by Oleanane Triterpenoides: Comparison of Glycyrrhizin and Its Aglycone 18α— and 18β-GIycyrrhetinic Acid Stereo— isomers, Carcinogenesis, 12, pp. 187-192, (1991)
[8]  
Agarwal R., Wang Z.Y., Mukhtar H., Inhibition of Skin Tumor Initiating Activity of 7, 12-Dimethyl— benz[a]anthracene by Chronic Oral Feeding of Glycyrrhizin in Drinking Water to Sencar Mice, Nutr Cancer, 15, pp. 187-193, (1991)
[9]  
Wang Z.Y., Das M., Bickers D.R., Mukhtar H., Interaction of Epicatechins Derived From Green Tea With Rat Hepatic Cytochrome P-450, Drug Metab Dispos, 16, pp. 98-103, (1988)
[10]  
Wang Z.Y., Cheng S.J., Zhou Z.C., Athar M., Khan W.A., Et al., Antimutagenic Activity of Green Tea Polyphenols, Mutat Res, 223, pp. 273-289, (1989)