Comparative evaluation of the chemopreventive efficacy of green and black tea polyphenols in the hamster buccal pouch carcinogenesis model

被引:17
作者
Mohan, KVPC
Hara, Y
Abraham, SK
Nagini, S [1 ]
机构
[1] Annamalai Univ, Fac Sci, Dept Biochem & Biotechnol, Annamalainagar 608002, Tamil Nadu, India
[2] Tokyo Food Techno Co Ltd, Shizuoka, Japan
[3] Jawaharlal Nehru Univ, Sch Life Sci, New Delhi 110067, India
关键词
chemoprevention; hamster buccal pouch carcinogenesis; polyphenon-E; polyphenon-B;
D O I
10.1016/j.clinbiochem.2005.06.011
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: To evaluate the comparative chemopreventive efficacy of green tea polyphenols (Polyphenon-E) and black tea polyphenols (Polyphenon-B) on 7,12-dimethylbenz[a]anthracene (DMBA)-induced hamster buccal pouch (HBP) carcinogenesis. Design and methods: Hamsters were divided into 6 groups. Animals in group 1 served as controls. Animals in groups 2 and 3 were administered 0.05% Polyphenon-E and B, respectively, in the diet. The right buccal pouches of animals in groups 4-6 were painted with 0.5% DMBA three times a week for 14 weeks. While group 4 received no further treatment, hamsters in groups 5 and 6 received diet containing 0.05% Polyphenon-E and B, respectively. The status of carcinogen-metabolising enzymes, lipid peroxidation and glutathione-dependent antioxidants in the buccal pouch and liver, as well as the frequency of bone marrow micronuclei were used as biomarkers. Results: Application of DMBA induced HBP carcinomas, increased genotoxicity with an imbalance in carcinogen-metabolising enzymes and the cellular redox status. Inhibition of HBP carcinomas by Polyphenon-E and B was associated with a significant decrease in phase I enzymes, modulation of lipid pet-oxidation and enhanced antioxidant and phase 11 enzyme activities. Conclusion: The greater efficacy of Polyphenon-B in inhibiting HBP carcinogenesis suggests that it may have a major impact in the chemoprevention of oral cancer. (c) 2005 The Canadian Society of Clinical Chemists. All rights reserved.
引用
收藏
页码:879 / 886
页数:8
相关论文
共 39 条
[1]   Glutathione and its metabolizing enzymes in patients with different benign and malignant diseases [J].
Abou Ghalia, AH ;
Fouad, IM .
CLINICAL BIOCHEMISTRY, 2000, 33 (08) :657-662
[2]   Cytochrome P450 and glutathione transferase expression in squamous cell cancer [J].
Ali, S ;
El-Rayes, BF ;
Heilbrun, LK ;
Sarkar, FH ;
Ensley, JF ;
Kucuk, O ;
Philip, PA .
CLINICAL CANCER RESEARCH, 2004, 10 (13) :4412-4416
[3]  
ANDERSON ME, 1982, METHOD ENZYMOL, V113, P548
[4]   Of humans and hamsters: comparative analysis of lipid peroxidation, glutathione, and glutathione-dependent enzymes during oral carcinogenesis [J].
Balasenthil, S ;
Saroja, M ;
Ramachandran, CR ;
Nagini, S .
BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY, 2000, 38 (04) :267-270
[5]  
Begleiter A, 2004, METHOD ENZYMOL, V382, P320
[6]   Combination chemoprevention by tomato and garlic in the hamster buccal pouch carcinogenesis model [J].
Bhuvaneswari, V ;
Mohan, KVPC ;
Nagini, S .
NUTRITION RESEARCH, 2004, 24 (02) :133-146
[7]   Effects of black tea, green tea and wine extracts on intestinal carcinogenesis induced by azoxymethane in F344 rats [J].
Caderni, G ;
De Filippo, C ;
Luceri, C ;
Salvadori, M ;
Giannini, A ;
Biggeri, A ;
Remy, S ;
Cheynier, V ;
Dolara, P .
CARCINOGENESIS, 2000, 21 (11) :1965-1969
[8]   INFLUENCE OF N-3 FATTY-ACIDS ON THE GROWTH OF HUMAN BREAST-CANCER CELLS IN-VITRO - RELATIONSHIP TO PEROXIDES AND VITAMIN-E [J].
CHAJES, V ;
SATTLER, W ;
STRANZL, A ;
KOSTNER, GM .
BREAST CANCER RESEARCH AND TREATMENT, 1995, 34 (03) :199-212
[10]   DT-diaphorase: a target for new anticancer drugs [J].
Danson, S ;
Ward, TH ;
Butler, J ;
Ranson, M .
CANCER TREATMENT REVIEWS, 2004, 30 (05) :437-449