Prevention of carcinogenesis by tea polyphenols

被引:63
作者
Yang, CS
Prabhu, S
Landau, J
机构
[1] Rutgers State Univ, Coll Pharm, Canc Res Lab, Piscataway, NJ 08854 USA
[2] Environm & Occupat Hlth Sci Inst, Piscataway, NJ 08854 USA
关键词
tea; biotransformation; carcinogenesis;
D O I
10.1081/DMR-120000651
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tea, an extract of the leaves of the plant Camellia sinensis, has been considered a medicine and healthful beverage for ages. The beneficial effects of tea are thought to be due to its polyphenolic components. Herein, we discuss the present status of tea as a possible cancer chemopreventive agent, covering basic chemistry and biochemical activity of tea, pharmacokinetics of major tea components, studies in animal and cell lines, epidemiological investigations, and future challenges. Tea is one of the few chemopreventive agents known to have protective effects at different stages of the carcinogenic process. Tea constituents may inhibit this process by modulating signal transduction pathways leading to the inhibition of cell proliferation and transformation and enhancement of apoptosis. These activities may or may not be due to the antioxidative activity of tea polyphenols. The bioavailability and tissue levels of tea polyphenols is a key topic to be studied in order to understand the mechanisms of action of tea and its possible protection against cancer in humans.
引用
收藏
页码:237 / 253
页数:17
相关论文
共 100 条
[71]   Implications of the mechanisms of action of tea polyphenols as antioxidants in vitro for chemoprevention in humans [J].
Rice-Evans, C .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 220 (04) :262-266
[72]   Structure-antioxidant activity relationships of flavonoids and phenolic acids [J].
RiceEvans, CA ;
Miller, NJ ;
Paganga, G .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (07) :933-956
[73]   Black tea and mammary gland carcinogenesis by 7,12-dimethylbenz[a]anthracene in rats fed control or high fat diets [J].
Rogers, AE ;
Hafer, LJ ;
Iskander, YS ;
Yang, S .
CARCINOGENESIS, 1998, 19 (07) :1269-1273
[74]  
SAKATA K, 1995, P SAN ANT BREAST CAN, V101
[75]   POLYPHENOLIC FLAVANOLS AS SCAVENGERS OF AQUEOUS-PHASE RADICALS AND AS CHAIN-BREAKING ANTIOXIDANTS [J].
SALAH, N ;
MILLER, NJ ;
PAGANGA, G ;
TIJBURG, L ;
BOLWELL, GP ;
RICEEVANS, C .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 322 (02) :339-346
[76]   Evidence for the interaction between (-)-epigallocatechin gallate and human plasma proteins fibronectin, fibrinogen, and histidine-rich glycoprotein [J].
Sazuka, M ;
Itoi, T ;
Suzuki, Y ;
Odani, S ;
Koide, T ;
Isemura, M .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1996, 60 (08) :1317-1319
[77]   Tea as a potential chemopreventive agent in PhIP carcinogenesis: Effects of green tea and black tea on PhIP-DNA adduct formation in female F-344 rats [J].
Schut, HAJ ;
Yao, RS .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2000, 36 (01) :52-58
[78]  
SHI ST, 1994, CANCER RES, V54, P4641
[79]   Comparative chemopreventive mechanisms of green tea, black tea and selected polyphenol extracts measured by in vitro bioassays [J].
Steele, VE ;
Kelloff, GJ ;
Balentine, D ;
Boone, CW ;
Mehta, R ;
Bagheri, D ;
Sigman, CC ;
Zhu, SY ;
Sharma, S .
CARCINOGENESIS, 2000, 21 (01) :63-67
[80]   LUNG-CANCER RISK AND MUTAGENICITY OF TEA [J].
TEWES, FJ ;
KOO, LC ;
MEISGEN, TJ ;
RYLANDER, R .
ENVIRONMENTAL RESEARCH, 1990, 52 (01) :23-33