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Article type: Research Article
Authors: Chung S. Yang, | Jee Y. Chung, | Guang-yu Yang, | Chuan Li, | Xiaofeng Meng, | Mao-Jung Lee,
Affiliations: Laboratory for Cancer Research, College of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854-8020, USA
Note: [] Laboratory for Cancer Research, College of Pharmacy, Rutgers, The State University of New Jersey, 164 Frelinghuysen Road, Piscataway, NJ 08854-8020, USA. Tel.: +1 732 445 5361; Fax: +1 732 445 0687; E-mail: [email protected]
Abstract: Tea {\it (Camellia sinensis)} preparations have been shown to inhibit tumorigenesis at the initiation, promotion, and progression stages in different animal models. The anti-proliferative effects of tea polyphenols may be a key mechanism, especially in the NNK-induced lung tumorigenesis model with mice. Studies with cell lines have demonstrated that tea polyphenols inhibit cell proliferation and induce apoptosis. The effective concentrations used in these studies (20--100 \muM) are usually higher than those observed in blood and tissues of humans and animals, which are in the low micromolar range. Glucuronide and sulfate conjugated and methylated catechins as well as ring fission products (due to intestinal microflora) have been observed in human plasma and urine. Purified green and black tea polyphenols inhibited the H-{\it ras} induced mitogen-activated protein kinases, AP-1 activities, and the growth of 30.7b Ras 12 and BES21 cells. Among the catechins, both the galloyl structure on the B ring and the gallate moiety are important for the inhibition. Both (-)-epigallocatechin-3-gallate and theaflavin-3,3'-digallate inhibited the phosphorylation of c-jun and p44/42 (ERK 1/2). More mechanistic and human studies in these areas will help us to understand the possible inhibitory action of tea against carcinogenesis in humans. Abbreviations: EGCG, (-)-epigallocatechin-3-gallate; EGC, (-)-epigallocatechin; ECG, (-)-epicatechin-3-gallate; EC, (-)-epicatechin; NNK, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone; DGT, decaffeinated green tea; MAP kinase, mitogen activating protein kinase; AP-1, activator protein-1; NF\kappaB, nucleoprotein factor \kappaB.
Journal: BioFactors, vol. 13, no. 1-4, pp. 73-79, 2000
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