Literature DB >> 10202396

Cancer chemopreventive mechanisms of tea against heterocyclic amine mutagens from cooked meat.

R H Dashwood1, M Xu, J F Hernaez, N Hasaniya, K Youn, A Razzuk.   

Abstract

Cooking meat and fish under normal conditions produces heterocyclic amine mutagens, several of which have been shown to induce colon tumors in experimental animals. In our search for natural dietary components that might protect against these mutagens, it was found that green tea and black tea inhibit the formation of heterocyclic amine-induced colonic aberrant crypt foci (ACF) in the rat. Since ACF are considered to be putative preneoplastic lesions, we examined the inhibitory mechanisms of tea against the heterocyclic amines. In the initial studies using the Salmonella mutagenicity assay, green tea and black tea inhibited according to the concentration of tea leaves during brewing and the time of brewing; a 2-3-min brew of 5% green tea (w/v) was sufficient for >90% antimutagenic activity. N-hydroxylated heterocyclic amines, which are direct-acting mutagens in Salmonella, were inhibited by complete tea beverage and by individual components of tea, such as epigallocatechin-3-gallate (EGCG). Inhibition did not involve enhanced mutagen degradation, and EGCG and other catechins complexed only weakly with the mutagens, suggesting electrophile scavenging as an alternative mechanism. Enzymes that contribute to the metabolic activation of heterocyclic amines, namely microsomal NADPH-cytochrome P450 reductase and N, O-acetyltransferase, were inhibited by tea in vitro. Studies in vivo established that tea also induces cytochromes P450 and Phase II enzymes in a manner consistent with the rapid metabolism and excretion of heterocyclic amines. Collectively, the results indicate that tea possesses anticarcinogenic activity in the colon, and this most likely involves multiple inhibitory mechanisms.

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Year:  1999        PMID: 10202396      PMCID: PMC2268949          DOI: 10.1046/j.1525-1373.1999.d01-41.x

Source DB:  PubMed          Journal:  Proc Soc Exp Biol Med        ISSN: 0037-9727


  27 in total

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Journal:  Carcinogenesis       Date:  1992-08       Impact factor: 4.944

Review 2.  Inhibition of carcinogenesis by minor dietary constituents.

Authors:  L W Wattenberg
Journal:  Cancer Res       Date:  1992-04-01       Impact factor: 12.701

3.  Possible mechanisms of antimutagens by various teas as judged by their effects on mutagenesis by 2-amino-3-methylimidazo[4,5-f]quinoline and benzo[a]pyrene.

Authors:  H Y Chen; G C Yen
Journal:  Mutat Res       Date:  1997-09-18       Impact factor: 2.433

4.  Inhibition of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ)-DNA binding by chlorophyllin: studies of enzyme inhibition and molecular complex formation.

Authors:  R Dashwood; D Guo
Journal:  Carcinogenesis       Date:  1992-07       Impact factor: 4.944

5.  Suppression of genotoxicity of carcinogens by (-)-epigallocatechin gallate.

Authors:  H Hayatsu; N Inada; T Kakutani; S Arimoto; T Negishi; K Mori; T Okuda; I Sakata
Journal:  Prev Med       Date:  1992-05       Impact factor: 4.018

6.  Observation and quantification of aberrant crypts in the murine colon treated with a colon carcinogen: preliminary findings.

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Authors:  S A Stopera; L C Murphy; R P Bird
Journal:  Carcinogenesis       Date:  1992-11       Impact factor: 4.944

8.  Antimutagenic activity of tea towards 2-hydroxyamino-3-methylimidazo[4,5-f]quinoline: effect of tea concentration and brew time on electrophile scavenging.

Authors:  J F Hernaez; M Xu; R H Dashwood
Journal:  Mutat Res       Date:  1998-06-18       Impact factor: 2.433

9.  Reduction of aberrant crypt formation in the colon of CF1 mice by potential chemopreventive agents.

Authors:  L K Lam; J Zhang
Journal:  Carcinogenesis       Date:  1991-12       Impact factor: 4.944

10.  Aberrant crypts: putative preneoplastic foci in human colonic mucosa.

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Journal:  Cancer Res       Date:  1991-03-01       Impact factor: 12.701

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3.  Dietary spinach reshapes the gut microbiome in an Apc-mutant genetic background: mechanistic insights from integrated multi-omics.

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