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Title

Grape antioxidant dietary fiber inhibits intestinal polyposis in ApcMin/+ mice: Relation to cell cycle and immune response

AuthorsSánchez-Tena, S.; Lizárraga, Daneida; Miranda, Agustín R.; Vinardell, M. Pilar ; García-García, Francisco; Dopazo, Joaquín; Torres, Josep Lluís ; Saura Calixto, Fulgencio D. ; Capellá, Gabriel; Cascante, Marta
Issue Date2013
PublisherOxford University Press
CitationCarcinogenesis 34: 1881- 1888 (2013)
AbstractEpidemiological and experimental studies suggest that fiber and phenolic compounds might have a protective effect on the development of colon cancer in humans. Accordingly, we assessed the chemopreventive efficacy and associated mechanisms of action of a lyophilized red grape pomace containing proanthocyanidin (PA)-rich dietary fiber [grape antioxidant dietary fiber (GADF)] on spontaneous intestinal tumorigenesis in the ApcMin/+ mouse model. Mice were fed a standard diet (control group) or a 1% (w/w) GADF-supplemented diet (GADF group) for 6 weeks. GADF supplementation greatly reduced intestinal tumorigenesis, significantly decreasing the total number of polyps by 76%. Moreover, size distribution analysis showed a considerable reduction in all polyp size categories [diameter <1 mm (65%), 1-2 mm (67%) and >2 mm (87%)]. In terms of polyp formation in the proximal, middle and distal portions of the small intestine, a decrease of 76, 81 and 73% was observed, respectively. Putative molecular mechanisms underlying the inhibition of intestinal tumorigenesis were investigated by comparison of microarray expression profiles of GADF-treated and non-treated mice. We observed that the effects of GADF are mainly associated with the induction of a G1 cell cycle arrest and the downregulation of genes related to the immune response and inflammation. Our findings show for the first time the efficacy and associated mechanisms of action of GADF against intestinal tumorigenesis in ApcMin/+ mice, suggesting its potential for the prevention of colorectal cancer. © The Author 2013. Published by Oxford University Press. All rights reserved.
URIhttp://hdl.handle.net/10261/87553
DOI10.1093/carcin/bgt140
Identifiersdoi: 10.1093/carcin/bgt140
issn: 0143-3334
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