Novel Mechanisms of Anticancer Activities of Green Tea Component Epigallocatechin-3-Gallate

被引:21
作者
Zhang, Le [1 ]
Wei, Yaqing [1 ]
Zhang, Jinsong [1 ]
机构
[1] Anhui Agr Univ China, Key Lab Tea Biochem & Biotechnol, Hefei 230036, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Cancer prevention; cancer therapy; epigallocatechin-3-gallate; 67-kDa laminin receptor; thioredoxin system; tea; LAMININ-BINDING PROTEIN; MAMMALIAN THIOREDOXIN REDUCTASE; GROWTH-FACTOR RECEPTOR; ORAL POLYPHENON E; RAI STAGE 0; PROSTATE-CANCER; (-)-EPIGALLOCATECHIN GALLATE; SIGNALING PATHWAYS; HYDROGEN-PEROXIDE; MOUSE MODEL;
D O I
10.2174/1871520614666140521114327
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
After water, tea is the most widely consumed beverage. The major active constituents in green tea are catechins, of which epigallocatechin-3-gallate (EGCG) is the most abundant and active compound. Animal experimental studies using EGCG alone or green tea catechins with EGCG being a major component have generated a mounting body of evidence suggesting that EGCG as a naturally occurring compound and commonly consumed beverage ingredient is a promising cancer preventive agent. However, the relationship between green tea consumption and reduced cancer risk seen from epidemiologic studies is not as encouraging as that observed in animal studies and remains inconclusive. In the present article, the achievements using EGCG or green tea catechins for cancer prevention were reviewed, the latest identified anticancer mechanisms of EGCG and the emerging mechanism-based cancer therapies of EGCG were outlined, and the potential reasons for the discrepancy in animal studies and epidemiological studies were tentatively analysed. On the basis of these analyses, it could be anticipated that future intervention trials in humans would be able to achieve consistent cancer prevention effects provided that the timely intervention of EGCG or green tea catechins at appropriate high-dose levels presumably approaching their upper safety limits have had been fully considered.
引用
收藏
页码:779 / 786
页数:8
相关论文
共 114 条
[1]   Effective Prostate Cancer Chemopreventive Intervention with Green Tea Polyphenols in the TRAMP Model Depends on the Stage of the Disease [J].
Adhami, Vaclar Mustafa ;
Siddiqui, Imtiaz Ahmad ;
Sarfaraz, Sami ;
Khwaja, Sabih Islam ;
Bin Hafeez, Bilal ;
Ahmad, Nihal ;
Mukhtar, Hasan .
CLINICAL CANCER RESEARCH, 2009, 15 (06) :1947-1953
[2]   Oral consumption of green tea polyphenols inhibits insulin-like growth factor-i-induced signaling in an autochthonous mouse model of prostate cancer [J].
Adhami, VM ;
Siddiqui, IA ;
Ahmad, N ;
Gupta, S ;
Mukhtar, H .
CANCER RESEARCH, 2004, 64 (23) :8715-8722
[3]   Metal-catalyzed oxidation of protein-bound dopamine [J].
Akagawa, Mitsugu ;
Ishii, Yoshihisa ;
Ishii, Takeshi ;
Shibata, Takahiro ;
Yotsu-Yamashita, Mari ;
Suyama, Kyozo ;
Uchida, Koji .
BIOCHEMISTRY, 2006, 45 (50) :15120-15128
[4]   Selenoproteins-What unique properties can arise with selenocysteine in place of cysteine? [J].
Arner, Elias S. J. .
EXPERIMENTAL CELL RESEARCH, 2010, 316 (08) :1296-1303
[5]   NITRIC-OXIDE ACTIVATES GUANYLATE CYCLASE AND INCREASES GUANOSINE 3'-5'-CYCLIC MONOPHOSPHATE LEVELS IN VARIOUS TISSUE PREPARATIONS [J].
ARNOLD, WP ;
MITTAL, CK ;
KATSUKI, S ;
MURAD, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (08) :3203-3207
[6]   Green tea (Camellia sinensis) for the prevention of cancer [J].
Boehm, Katja ;
Borrelli, Francesca ;
Ernst, Edzard ;
Habacher, Gabi ;
Hung, Shao Kang ;
Milazzo, Stefania ;
Horneber, Markus .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2009, (03)
[7]   The major green tea polyphenol, (-)-epigallocatechin-3-gallate, inhibits obesity, metabolic syndrome, and fatty liver disease in high-fat-fed mice [J].
Bose, Mousumi ;
Lambert, Joshua D. ;
Ju, Jihyeung ;
Reuhl, Kenneth R. ;
Shapses, Sue A. ;
Yang, Chung S. .
JOURNAL OF NUTRITION, 2008, 138 (09) :1677-1683
[8]  
Chen J, 2012, TRANSL GASTROINTEST, V1, P243, DOI DOI 10.3978/J.ISSN.2224-4778.2012.09.04
[9]   Peracetylated (-)-epigallocatechin-3-gallate (AcEGCG) potently prevents skin carcinogenesis by suppressing the PKD1-dependent signaling pathway in CD34+ skin stem cells and skin tumors [J].
Chiou, Yi-Shiou ;
Sang, Shengmin ;
Cheng, Kuang-Hung ;
Ho, Chi-Tang ;
Wang, Ying-Jan ;
Pan, Min-Hsiung .
CARCINOGENESIS, 2013, 34 (06) :1315-1322
[10]   Specific induction of glutathione S-transferase GSTM2 subunit expression by epigallocatechin gallate in rat liver [J].
Chou, FP ;
Chu, YC ;
Hsu, JD ;
Chiang, HC ;
Wang, CJ .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (05) :643-650