Green tea and black tea consumption in relation to colorectal cancer risk: the Singapore Chinese Health Study.

The relationships between green tea and black tea consumption and colorectal cancer risk were examined within the Singapore Chinese Health Study, a prospective cohort study of diet and cancer involving >60,000 men and women. Intake of green tea and black tea was assessed through in-person interviews. Incident cancer cases and deaths among cohort members were identified through record linkage of the cohort database with respective databases from the nationwide Singapore Cancer Registry and the Singapore Registry of Births and Deaths. The proportional hazard regression method was used to examine the associations between intake of green and black tea separately and colorectal cancer risk with adjustment for potential confounders. After an average of 8.9 years of follow-up, 845 colorectal cancer cases were identified. Subjects who drank green tea exhibited a statistically non-significant increase in risk [relative risk (RR) = 1.12, 95% confidence interval (CI) = 0.97-1.29] relative to non-drinkers of green tea. This risk increase was mainly confined to men (RR = 1.31, 95% CI = 1.08-1.58); the comparable RR in women was 0.89 (95% CI = 0.71-1.12). In men, the green tea-colorectal cancer association was noted mainly in those with advanced disease (Duke C or D) (RR = 1.53, 95% CI = 1.19-1.97), and the association was dose dependent (P for trend = 0.0002). This latter association was especially strong within the colon subsite (RR = 1.75, 95% CI = 1.24-2.46; P for trend < 0.0001). Irrespective of gender, intake of black tea was not associated with risk of colorectal cancer (RR = 0.92, 95% CI = 0.79-1.07) in this Asian population.

[1]  D. Ferreira,et al.  Hypoxia-inducible factor-1 activation by (-)-epicatechin gallate: potential adverse effects of cancer chemoprevention with high-dose green tea extracts. , 2004, Journal of natural products.

[2]  Y. Schneider,et al.  Suppression of Azoxymethane-Induced Preneoplastic Lesions and Inhibition of Cyclooxygenase-2 Activity in the Colonic Mucosa of Rats Drinking a Crude Green Tea Extract , 2000, Nutrition and cancer.

[3]  F. Kadlubar,et al.  Chemoprotection against the formation of colon DNA adducts from the food-borne carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in the rat. , 1997, Mutation research.

[4]  B. Pittman,et al.  Tea polyphenols as inhibitors of mutagenicity of major classes of carcinogens. , 1996, Mutation research.

[5]  R. Dashwood,et al.  Antimutagenic activity of tea towards 2-hydroxyamino-3-methylimidazo[4,5-f]quinoline: effect of tea concentration and brew time on electrophile scavenging. , 1998, Mutation research.

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

[7]  H. Schut,et al.  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 , 2000, Nutrition and cancer.

[8]  Jian-Min Yuan,et al.  Diabetes mellitus and risk of colorectal cancer in the Singapore Chinese Health Study. , 2006, Journal of the National Cancer Institute.

[9]  C. Vecchia,et al.  Coffee, Decaffeinated Coffee, Tea and Cancer of the Colon and Rectum: A Review of Epidemiological Studies, 1990-2003 , 2004, Cancer Causes & Control.

[10]  Y. Lou,et al.  Inhibitory effects of black tea, green tea, decaffeinated black tea, and decaffeinated green tea on ultraviolet B light-induced skin carcinogenesis in 7,12-dimethylbenz[a]anthracene-initiated SKH-1 mice. , 1994, Cancer research.

[11]  W. Koh,et al.  Cigarettes and alcohol in relation to colorectal cancer: the Singapore Chinese Health Study , 2007, British Journal of Cancer.

[12]  A. Murakami,et al.  (-)-Epigallocatechin-3-gallate promotes pro-matrix metalloproteinase-7 production via activation of the JNK1/2 pathway in HT-29 human colorectal cancer cells. , 2005, Carcinogenesis.

[13]  Jian-Min Yuan,et al.  Urinary biomarkers of tea polyphenols and risk of colorectal cancer in the Shanghai Cohort Study , 2007, International journal of cancer.

[14]  H. Schut,et al.  Protection by green tea, black tea, and indole-3-carbinol against 2-amino-3-methylimidazo[4,5-f]quinoline-induced DNA adducts and colonic aberrant crypts in the F344 rat. , 1996, Carcinogenesis.

[15]  P. Vaupel,et al.  Tumor hypoxia: definitions and current clinical, biologic, and molecular aspects. , 2001, Journal of the National Cancer Institute.

[16]  X. Jia,et al.  Effects of Green Tea on Colonic Aberrant Crypt Foci and Proliferative Indexes in Rats , 2001, Nutrition and cancer.

[17]  D. Cox Regression Models and Life-Tables , 1972 .

[18]  Jian-Min Yuan,et al.  Green tea, black tea and colorectal cancer risk: a meta-analysis of epidemiologic studies. , 2006, Carcinogenesis.

[19]  T. Ishikawa,et al.  Matrilysin is associated with progression of colorectal tumor. , 1996, Cancer letters.

[20]  Rusha Thomas,et al.  Epigallocatechin gallate inhibits HIF-1α degradation in prostate cancer cells , 2005 .

[21]  D.,et al.  Regression Models and Life-Tables , 2022 .

[22]  D O Stram,et al.  Singapore Chinese Health Study: Development, Validation, and Calibration of the Quantitative Food Frequency Questionnaire , 2001, Nutrition and cancer.

[23]  Z. Apostolides,et al.  Inhibition of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) mutagenicity by black and green tea extracts and polyphenols. , 1996, Mutation research.

[24]  N. Hébert-croteau A meta-analysis of hormone replacement therapy and colon cancer in women. , 1998, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[25]  W. Koh,et al.  Tea and circulating estrogen levels in postmenopausal Chinese women in Singapore. , 2005, Carcinogenesis.

[26]  M. Hirose,et al.  Green tea catechins enhance tumor development in the colon without effects in the lung or thyroid after pretreatment with 1,2-Dimethylhydrazine or 2,2'-dihydroxy-di-n-propylnitrosamine in male F344 rats. , 2001, Cancer letters.

[27]  K. Machens,et al.  Estrogen plus progestin and colorectal cancer in postmenopausal women. , 2004, The New England journal of medicine.

[28]  C. Perneel,et al.  Hypoxia in human colorectal adenocarcinoma: comparison between extrinsic and potential intrinsic hypoxia markers. , 2006, International journal of radiation oncology, biology, physics.

[29]  W. Willett,et al.  Coffee, tea, and caffeine consumption and incidence of colon and rectal cancer. , 2005, Journal of the National Cancer Institute.

[30]  R. Chlebowski,et al.  Estrogen plus progestin and colorectal cancer in postmenopausal women. , 2004, The New England journal of medicine.

[31]  D A Hilton,et al.  Overexpression of hypoxia-inducible factor 1alpha in common human cancers and their metastases. , 1999, Cancer research.

[32]  John Robbins,et al.  National cross sectional survey to determine whether the decision to delivery interval is critical in emergency caesarean section , 2004, BMJ : British Medical Journal.

[33]  N. Laird,et al.  Meta-analysis in clinical trials. , 1986, Controlled clinical trials.

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

[35]  A. Murakami,et al.  ( )-Epigallocatechin-3-gallate promotes pro-matrix metalloproteinase-7 production via activation of the JNK 1 / 2 pathway in HT-29 human colorectal cancer cells , 2005 .

[36]  J. Waterhouse Cancer incidence in five continents, v.3 , 1976 .

[37]  U. Jagadeesan An Incentive to Start Hormone Replacement: The Effect of Postmenopausal Hormone Replacement Therapy on the Risk of Colorectal Cancer , 2002, Journal of the American Geriatrics Society.