Literature DB >> 11807163

Inhibition of carcinogenesis by tea.

Chung S Yang1, Pius Maliakal, Xiaofeng Meng.   

Abstract

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.

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Year:  2002        PMID: 11807163     DOI: 10.1146/annurev.pharmtox.42.082101.154309

Source DB:  PubMed          Journal:  Annu Rev Pharmacol Toxicol        ISSN: 0362-1642            Impact factor:   13.820


  163 in total

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2.  Genetic Association Between the COMT Genotype and Urinary Levels of Tea Polyphenols and Their Metabolites among Daily Green Tea Drinkers.

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Journal:  Int J Mol Epidemiol Genet       Date:  2010

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Authors:  Fa Chen; Baochang He; Zhijian Hu; Jiangfeng Huang; Fangping Liu; Lingjun Yan; Zheng Lin; Xiaoyan Zheng; Lisong Lin; Zuofeng Zhang; Lin Cai
Journal:  J Cancer Res Clin Oncol       Date:  2016-02-02       Impact factor: 4.553

5.  Harmine is an ATP-competitive inhibitor for dual-specificity tyrosine phosphorylation-regulated kinase 1A (Dyrk1A).

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6.  Modulation of folate uptake in cultured human colon adenocarcinoma Caco-2 cells by dietary compounds.

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7.  Structural identification of novel glucoside and glucuronide metabolites of (-)-epigallocatechin-3-gallate in mouse urine using liquid chromatography/electrospray ionization tandem mass spectrometry.

Authors:  Shengmin Sang; Chung S Yang
Journal:  Rapid Commun Mass Spectrom       Date:  2008-11       Impact factor: 2.419

8.  Interaction between rice bran albumin and epigallocatechin gallate and their physicochemical analysis.

Authors:  Rui Yang; Yuqian Liu; Jingjing Xu; Wenting Shang; Xiao Yu; Yongjin Wang; Chris Blanchard; Zhongkai Zhou
Journal:  Food Sci Biotechnol       Date:  2018-05-29       Impact factor: 2.391

Review 9.  Laboratory, epidemiological, and human intervention studies show that tea (Camellia sinensis) may be useful in the prevention of obesity.

Authors:  Kimberly A Grove; Joshua D Lambert
Journal:  J Nutr       Date:  2010-01-20       Impact factor: 4.798

10.  Coffee, tea, caffeine intake, and risk of adult glioma in three prospective cohort studies.

Authors:  Crystal N Holick; Scott G Smith; Edward Giovannucci; Dominique S Michaud
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2010-01       Impact factor: 4.254

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