Inhibition of N-methyl-N'-nitro-N-nitrosoguanidine-induced carcinogenesis by (-)-epigallocatechin gallate in the rat glandular stomach

Author(s): Yamane T, Takahashi T, Kuwata K, Oya K, Inagake M, et al.

Abstract

Recently, an epidemiological study showed a lower risk of gastric cancer among people who consume a large amount of green tea. (-)-Epigallocatechin gallate (EGCG), one of the main constituents of green tea, inhibited tumor promotion by teleocidin in a two-stage carcinogenesis experiment with the use of mouse skin. The inhibitory effect of EGCG on N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced carcinogenesis of the glandular stomach in rats was examined. The percentage of tumor-bearing rats in the group treated with MNNG plus EGCG was 31%, compared to 62% in the MNNG group. The difference was statistically significant (P < 0.05). To assess the effect of p.o. administration of EGCG, the gastric mucosal cellular kinetics was examined with the use of the bromodeoxyuridine labeling index, ornithine decarboxylase activity, and tissue polyamine levels. The labeling index of the EGCG treatment group decreased significantly (P < 0.05) compared to the EGCG plus MNNG treatment group. The ornithine decarboxylase activity and tissue spermidine levels were also decreased. On the other hand, the tissue putrescine and spermine levels were partly increased. These findings suggest that EGCG inhibits the cellular kinetics of the gastric mucosa during the promotion stage of MNNG-induced gastric carcinogenesis. EGCG may be useful in preventing gastric carcinogenesis. Moreover, EGCG may be applied clinically without any harmful effects and at a low cost.

Similar Articles

Inhibition of carcinogenesis by tea

Author(s): Yang CS, Maliakal P, Meng X

Prostate cancer chemoprevention by green tea

Author(s): Gupta S, Ahmad N, Mukhtar H

Apoptosis-inducing activity of high molecular weight fractions of tea extracts

Author(s): Hayakawa S, Kimura T, Saeki K, Koyama Y, Aoyagi Y, et al.

Apoptosis induction by epigallocatechin gallate involves its binding to Fas

Author(s): Hayakawa S, Saeki K, Sazuka M, Suzuki Y, Shoji Y, et al.

Synthetic analogs of green tea polyphenols as proteasome inhibitors

Author(s): Smith DM, Wang Z, Kazi A, Li LH, Chan TH, et al.

The proteasome: paradigm of a self-compartmentalizing protease

Author(s): Baumeister W, Walz J, Zühl F, Seemüller E

Activation domain-dependent monoubiquitylation of Gal4 protein is essential for promoter binding in vivo

Author(s): Archer CT, Delahodde A, Gonzalez F, Johnston SA, Kodadek T

Physical and functional association of RNA polymerase II and the proteasome

Author(s): Gillette TG, Gonzalez F, Delahodde A, Johnston SA, Kodadek T

Recruitment of a 19S proteasome subcomplex to an activated promoter

Author(s): Gonzalez F, Delahodde A, Kodadek T, Johnston SA

The 19S complex of the proteasome regulates nucleotide excision repair in yeast

Author(s): Gillette TG, Huang W, Russell SJ, Reed SH, Johnston SA, et al.

Distinct functions of the ubiquitin-proteasome pathway influence nucleotide excision repair

Author(s): Gillette TG, Yu S, Zhou Z, Waters R, Johnston SA, et al.

Synergistic effect of green tea catechins on cell growth and apoptosis induction in gastric carcinoma cells

Author(s): Horie N, Hirabayashi N, Takahashi Y, Miyauchi Y, Taguchi H, et al.

Lactacystin, proteasome function, and cell fate

Author(s): Fenteany G, Schreiber SL

Apoptosis induced by proteasome inhibition in cancer cells: predominant role of the p53/PUMA pathway

Author(s): Concannon CG, Koehler BF, Reimertz C, Murphy BM, Bonner C, et al.

Caspases and apoptosis

Author(s): Salvesen GS

NF-kappaB controls cell growth and differentiation through transcriptional regulation of cyclin D1

Author(s): Guttridge DC, Albanese C, Reuther JY, Pestell RG, Baldwin AS Jr

Tea polyphenols, their biological effects and potential molecular targets

Author(s): Chen D, Milacic V, Chen MS, Wan SB, Lam WH, et al.