Inhibition of carcinogenesis by tea.

Tea has received a great deal of attention because tea polyphenols are strong antioxidants, and tea preparations have inhibitory activity against tumorigenesis. The bioavailability and biotransformation of tea polyphenols, however, are key factors limiting these activities in vivo. The inhibition of tumorigenesis by green or black tea preparations has been demonstrated in animal models on different organ sites such as skin, lung, oral cavity, esophagus, forestomach, stomach, small intestine, colon, pancreas, and mammary gland. Epidemiological studies, however, have not yielded clear conclusions concerning the protective effects of tea consumption against cancer formation in humans. The discrepancy between the results from humans and animal models could be due to 1) the much higher doses of tea used in animals in comparison to human consumption, 2) the differences in causative factors between the cancers in humans and animals, and 3) confounding factors limiting the power of epidemiological studies to detect an effect. It is possible that tea may be only effective against specific types of cancer caused by certain etiological factors. Many mechanisms have been proposed for the inhibition of carcinogenesis by tea, including the modulation of signal transduction pathways that leads to the inhibition of cell proliferation and transformation, induction of apoptosis of preneoplastic and neoplastic cells, as well as inhibition of tumor invasion and angiogenesis. These mechanisms need to be evaluated and verified in animal models or humans in order to gain more understanding on the effect of tea consumption on human cancer.

[1]  M. Hirose,et al.  Post-initiation inhibitory effects of green tea catechins on 7,12-dimethylbenz[a]anthracene-induced mammary gland carcinogenesis in female Sprague-Dawley rats. , 1997, Cancer letters.

[2]  Hideyuki Ito,et al.  Wide distribution of [3H](-)-epigallocatechin gallate, a cancer preventive tea polyphenol, in mouse tissue. , 1998, Carcinogenesis.

[3]  Y. P. Lu,et al.  Inhibitory effect of black tea on the growth of established skin tumors in mice: effects on tumor size, apoptosis, mitosis and bromodeoxyuridine incorporation into DNA. , 1997, Carcinogenesis.

[4]  J. Terao,et al.  Dietary flavonoids as antioxidants in vivo: conjugated metabolites of (-)-epicatechin and quercetin participate in antioxidative defense in blood plasma. , 1999, The journal of medical investigation : JMI.

[5]  D. Alberts,et al.  Prevention of photocarcinogenesis by topical administration of pure epigallocatechin gallate isolated from green tea. , 1996, Nutrition and cancer.

[6]  J. Hodgson,et al.  Comparison of the effects of black and green tea on in vitro lipoprotein oxidation in human serum , 1999 .

[7]  F. Nanjo,et al.  Identification of (-)-epicatechin metabolites and their metabolic fate in the rat. , 1999, Drug metabolism and disposition: the biological fate of chemicals.

[8]  Toshio Takahashi,et al.  Inhibitory effects and toxicity of green tea polyphenols for gastrointestinal carcinogenesis , 1996, Cancer.

[9]  J. Bushman Green tea and cancer in humans: a review of the literature. , 1998, Nutrition and cancer.

[10]  C. Gardana,et al.  Catechin metabolites after intake of green tea infusions , 1998, BioFactors.

[11]  R. Mohan,et al.  Protection against induction of mouse skin papillomas with low and high risk of conversion to malignancy by green tea polyphenols. , 1997, Carcinogenesis.

[12]  D. Liebler,et al.  Antioxidant chemistry of green tea catechins. Identification of products of the reaction of (-)-epigallocatechin gallate with peroxyl radicals. , 1999, Chemical research in toxicology.

[13]  G. Yang,et al.  Black tea constituents, theaflavins, inhibit 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis in A/J mice. , 1997, Carcinogenesis.

[14]  S. Wiseman,et al.  The chemistry of tea flavonoids. , 1997, Critical reviews in food science and nutrition.

[15]  Yihai Cao,et al.  Angiogenesis inhibited by drinking tea , 1999, Nature.

[16]  D. August,et al.  Ingestion of green tea rapidly decreases prostaglandin E2 levels in rectal mucosa in humans. , 1999, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[17]  J. Klaunig,et al.  Chemopreventive effects of green and black tea on pulmonary and hepatic carcinogenesis. , 1996, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[18]  S. Wiseman,et al.  Antioxidants in tea. , 1997, Critical reviews in food science and nutrition.

[19]  G. Yang,et al.  Inhibition of growth and induction of apoptosis in human cancer cell lines by tea polyphenols. , 1998, Carcinogenesis.

[20]  M. Katdare,et al.  Inhibition of aberrant proliferation and induction of apoptosis in pre-neoplastic human mammary epithelial cells by natural phytochemicals. , 1998, Oncology reports.

[21]  H. Fujiki,et al.  Inhibition of N-methyl-N'-nitro-N-nitrosoguanidine-induced carcinogenesis by (-)-epigallocatechin gallate in the rat glandular stomach. , 1995, Cancer research.

[22]  J. Chen,et al.  Tea preparations protect against DMBA-induced oral carcinogenesis in hamsters. , 1999, Nutrition and cancer.

[23]  K. Nakachi,et al.  Cancer-preventive effects of drinking green tea among a Japanese population. , 1997, Preventive medicine.

[24]  H. Mukhtar,et al.  Mechanism of cancer chemopreventive activity of green Tea. , 1999, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[25]  M. Hirose,et al.  Inhibition of mammary gland carcinogenesis by green tea catechins and other naturally occurring antioxidants in female Sprague-Dawley rats pretreated with 7,12-dimethylbenz[alpha]anthracene. , 1994, Cancer letters.

[26]  K. Wakabayashi,et al.  Inhibitory effects of 1-O-hexyl-2,3,5-trimethylhydroquinone (HTHQ), green tea catechins and other antioxidants on 2-amino-6-methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1)-induced rat hepatocarcinogenesis and dose-dependent inhibition by HTHQ of lesion induction by Glu-P-1 or 2-amino-3,8-dimethylim , 1995, Carcinogenesis.

[27]  A. Yonemura,et al.  Inhibitory effect of tea flavonoids on the ability of cells to oxidize low density lipoprotein. , 1999, Biochemical pharmacology.

[28]  Weiya Ma,et al.  Inhibition of tumor promoter-induced activator protein 1 activation and cell transformation by tea polyphenols, (-)-epigallocatechin gallate, and theaflavins. , 1997, Cancer research.

[29]  G. Yang,et al.  Inhibition of carcinogenesis by tea: bioavailability of tea polyphenols and mechanisms of actions. , 1999, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[30]  G. Yang,et al.  Inhibition of spontaneous formation of lung tumors and rhabdomyosarcomas in A/J mice by black and green tea. , 1998, Carcinogenesis.

[31]  C. S. Yang,et al.  Bioavailability of flavonoids from tea. , 1997, Critical reviews in food science and nutrition.

[32]  S. Amin,et al.  Inhibition of tobacco-specific nitrosamine-induced lung tumorigenesis in A/J mice by green tea and its major polyphenol as antioxidants. , 1992, Cancer research.

[33]  H N Graham,et al.  Green tea composition, consumption, and polyphenol chemistry. , 1992, Preventive medicine.

[34]  Inhibitory Effect of Green Tea Extract on the Process of Pancreatic Carcinogenesis Induced by N‐Nitrosobis‐(2‐oxypropyl)amine (BOP) and on Tumor Promotion After Transplantation of N‐Nitrosobis‐(2‐hydroxypropyl)amine (BHP)‐Induced Pancreatic Cancer in Syrian Hamsters , 1997, Pancreas.

[35]  Jen-kun Lin,et al.  Suppression of extracellular signals and cell proliferation through EGF receptor binding by (−)‐epigallocatechin gallate in human A431 epidermoid carcinoma cells , 1997, Journal of cellular biochemistry.

[36]  J. Lin,et al.  Cancer chemoprevention by tea polyphenols through mitotic signal transduction blockade. , 1999, Biochemical pharmacology.

[37]  I. Dreosti,et al.  Protection by tea against UV-A + B-induced skin cancers in hairless mice. , 1998, Nutrition and cancer.

[38]  V. Steele,et al.  Effects of theaflavins on N-nitrosomethylbenzylamine-induced esophageal tumorigenesis. , 1997, Nutrition and cancer.

[39]  M. Hirose,et al.  Effects of green tea catechins on the progression or late promotion stage of mammary gland carcinogenesis in female Sprague-Dawley rats pretreated with 7,12-dimethylbenz(a)anthracene. , 1997, Cancer letters.

[40]  Y. P. Lu,et al.  Effects of oral administration of tea, decaffeinated tea, and caffeine on the formation and growth of tumors in high-risk SKH-1 mice previously treated with ultraviolet B light. , 1999, Nutrition and cancer.

[41]  H. Fujiki,et al.  Effect of (-)-epigallocatechin gallate, the main constituent of green tea, on lung metastasis with mouse B16 melanoma cell lines. , 1992, Cancer letters.

[42]  J K McLaughlin,et al.  Reduced risk of esophageal cancer associated with green tea consumption. , 1994, Journal of the National Cancer Institute.

[43]  M. Hirose,et al.  Phenolics: blocking agents for heterocyclic amine-induced carcinogenesis. , 1999, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[44]  Y. Hara,et al.  Inhibitory Effects of Tea Catechins, Black Tea Extract and Oolong Tea Extract on Hepatocarcinogenesis in Rat , 1996, Japanese journal of cancer research : Gann.

[45]  V. Steele,et al.  Effect of Tea Extracts, Polyphenols, and Epigallocatechin Gallate on Azoxymethane-induced Colon Cancer , 1998, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[46]  H. Mukhtar,et al.  Tea in chemoprevention of cancer. , 1996, International journal of oncology.

[47]  Jen-kun Lin,et al.  Inhibition of cyclin‐dependent kinases 2 and 4 activities as well as induction of cdk inhibitors p21 and p27 during growth arrest of human breast carcinoma cells by (−)‐epigallocatechin‐3‐gallate , 1999, Journal of cellular biochemistry.

[48]  G. Bowden,et al.  Inhibition of ultraviolet B–induced c‐fos gene expression and p38 mitogen‐activated protein kinase activation by (‐)‐epigallocatechin gallate in a human keratinocyte cell line , 1999, Molecular carcinogenesis.

[49]  M. Isemura,et al.  Effects of tea polyphenols on the invasion and matrix metalloproteinases activities of human fibrosarcoma HT1080 cells. , 1999, Journal of agricultural and food chemistry.

[50]  S. Amin,et al.  Inhibition of lung carcinogenesis by black tea in Fischer rats treated with a tobacco-specific carcinogen: caffeine as an important constituent. , 1998, Cancer research.

[51]  J. Terao,et al.  Accumulation of (-)-epicatechin metabolites in rat plasma after oral administration and distribution of conjugation enzymes in rat tissues. , 1998, The Journal of nutrition.

[52]  W. Chow,et al.  Cancer rates among drinkers of black tea. , 1997, Critical reviews in food science and nutrition.

[53]  N. Willits,et al.  The effects of phenethyl isothiocyanate, N-acetylcysteine and green tea on tobacco smoke-induced lung tumors in strain A/J mice. , 1998, Carcinogenesis.

[54]  Z. Yang,et al.  Green tea and its major components ameliorate immune dysfunction in mice bearing Lewis lung carcinoma and treated with the carcinogen NNK. , 1999, Nutrition and cancer.

[55]  May-Chen Kuo,et al.  Blood and urine levels of tea catechins after ingestion of different amounts of green tea by human volunteers. , 1998, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[56]  A. E. Rogers,et al.  Black tea and mammary gland carcinogenesis by 7,12-dimethylbenz[a]anthracene in rats fed control or high fat diets. , 1998, Carcinogenesis.

[57]  Y. Hara,et al.  Anti-tumor activity of tea catechins. , 1989 .

[58]  Y. Lou,et al.  Effects of tea, decaffeinated tea, and caffeine on UVB light-induced complete carcinogenesis in SKH-1 mice: demonstration of caffeine as a biologically important constituent of tea. , 1997, Cancer research.

[59]  A. Komori,et al.  Mechanisms of Growth Inhibition of Human Lung Cancer Cell Line, PC‐9, by Tea Polyphenols , 1997, Japanese journal of cancer research : Gann.

[60]  Z. Y. Wang,et al.  Tea and cancer. , 1993, Journal of the National Cancer Institute.

[61]  T. Nukiwa,et al.  Inhibitory effects of green tea infusion on in vitro invasion and in vivo metastasis of mouse lung carcinoma cells. , 1995, Cancer letters.

[62]  C. Rice-Evans,et al.  Implications of the mechanisms of action of tea polyphenols as antioxidants in vitro for chemoprevention in humans. , 1999, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[63]  Y. Shukla,et al.  Chemopreventive effects of black tea polyphenols in mouse skin model of carcinogenesis. , 1998, Biomedical and environmental sciences : BES.

[64]  F. Nanjo,et al.  Methylation of tea catechins by rat liver homogenates. , 1999, Bioscience, biotechnology, and biochemistry.

[65]  G. Yang,et al.  Characterization of early pulmonary hyperproliferation and tumor progression and their inhibition by black tea in a 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced lung tumorigenesis model with A/J mice. , 1997, Cancer Research.

[66]  N. Miyata,et al.  Scavenging mechanisms of (-)-epigallocatechin gallate and (-)-epicatechin gallate on peroxyl radicals and formation of superoxide during the inhibitory action. , 1999, Free radical biology & medicine.

[67]  R. Hiipakka,et al.  Growth inhibition and regression of human prostate and breast tumors in athymic mice by tea epigallocatechin gallate. , 1995, Cancer letters.

[68]  Maojung Lee,et al.  Absorption, Distribution, and Elimination of Tea Polyphenols in Rats , 1997 .

[69]  R. Agarwal,et al.  Green tea constituent epigallocatechin-3-gallate and induction of apoptosis and cell cycle arrest in human carcinoma cells. , 1997, Journal of the National Cancer Institute.

[70]  K. Nakagawa,et al.  Absorption and distribution of tea catechin, (-)-epigallocatechin-3-gallate, in the rat. , 1997, Journal of nutritional science and vitaminology.

[71]  T. Sugimura,et al.  Anticarcinogenic effects of (-)-epigallocatechin gallate. , 1992, Preventive medicine.

[72]  Y. L. Lin,et al.  Suppression of extracellular signals and cell proliferation by the black tea polyphenol, theaflavin-3,3'-digallate. , 1999, Carcinogenesis.

[73]  Z. Dong,et al.  Inhibition of activator protein 1 activity and cell growth by purified green tea and black tea polyphenols in H-ras-transformed cells: structure-activity relationship and mechanisms involved. , 1999, Cancer research.

[74]  F. Kok,et al.  Tea and cancer prevention: an evaluation of the epidemiologic literature. , 1997, Nutrition and cancer.

[75]  B. Pittman,et al.  Effect of black tea on azoxymethane-induced colon cancer. , 1998, Carcinogenesis.

[76]  M. Hirose,et al.  Effects of green tea catechins in a rat multi-organ carcinogenesis model. , 1993, Carcinogenesis.

[77]  R. Goldbohm,et al.  Consumption of black tea and cancer risk: a prospective cohort study. , 1996, Journal of the National Cancer Institute.

[78]  J. Weisburger,et al.  Tea, or tea and milk, inhibit mammary gland and colon carcinogenesis in rats. , 1997, Cancer letters.

[79]  D. Sato Inhibition of urinary bladder tumors induced by N‐butyl‐N‐(4‐hydroxybutyl)‐nitrosamine in rats by green tea , 1999, International journal of urology : official journal of the Japanese Urological Association.

[80]  Y. Konishi,et al.  Inhibitory effects of beta-carotene, palm carotene, and green tea polyphenols on pancreatic carcinogenesis initiated by N-nitorsobis(2-oxopropyl)amine in Syrian golden hamsters. , 1998, Pancreas.