Literature DB >> 9771930

Effects of dietary fat and a vegetable-fruit mixture on the development of intestinal neoplasia in the ApcMin mouse.

H J van Kranen1, P W van Iersel, J M Rijnkels, D B Beems, G M Alink, C F van Kreijl.   

Abstract

The variation in colorectal cancer (CRC) incidence worldwide strongly suggests a role for dietary influences. Based on epidemiological data, protective effects of vegetables and fruit intake on CRC are widely claimed, while other data indicate a possible increased CRC risk from (higher) dietary fat intake. Therefore, we have investigated single and interactive effects of dietary fat and a vegetable-fruit mixture (VFM) in the ApcMin mouse, a mouse model for multiple intestinal neoplasia. In this study, four different diets (A-D) were compared, which were either low in fat (20% energy diets A/B) or high in fat (40% energy diets C/D). In addition, 19.5% (wt/wt) of the carbohydrates in diets B and D were replaced by a freeze-dried VFM. The diets were balanced so that they only differed among each other in fat/carbohydrate content and the presence of specific plant-constituents. Because the initiation of intestinal tumors in ApcMin mice occurs relatively early in life, exposure to the diets was started in utero. Without the addition of VFM, mice maintained at a high-fat diet did not develop significantly higher numbers of small or large intestinal adenomas than mice maintained at a low-fat diet. VFM added to a low-fat diet significantly lowered multiplicity of small intestinal polyps (from 16.2 to 10.2/mouse, 15 animals/group), but not of colon tumors in male ApcMin mice only. Strikingly, addition of VFM to female mice maintained on a low-fat diet and to both sexes maintained on a high-fat diet significantly enhanced intestinal polyp multiplicity (from 16.5 to 26.7 polyps/mouse). In conclusion, our results indicate that neither a lower fat intake nor consumption of VFM included in a high-fat diet decreases the development of polyps in mice genetically predisposed to intestinal tumor development.

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Year:  1998        PMID: 9771930     DOI: 10.1093/carcin/19.9.1597

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  5 in total

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Authors:  Alexandra E Tammariello; John A Milner
Journal:  J Nutr Biochem       Date:  2010-02       Impact factor: 6.048

Review 2.  Obesity-Associated Cancers: Evidence from Studies in Mouse Models.

Authors:  Ho Lee
Journal:  Cells       Date:  2022-04-27       Impact factor: 7.666

Review 3.  Point: From animal models to prevention of colon cancer. Systematic review of chemoprevention in min mice and choice of the model system.

Authors:  Denis E Corpet; Fabrice Pierre
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2003-05       Impact factor: 4.254

4.  Nested case-control study on the risk factors of colorectal cancer.

Authors:  Kun Chen; Jian Cai; Xi-Yong Liu; Xi-Yuan Ma; Kai-Yan Yao; Shu Zheng
Journal:  World J Gastroenterol       Date:  2003-01       Impact factor: 5.742

5.  Metabolomics of ApcMin/+ mice genetically susceptible to intestinal cancer.

Authors:  Jean-Eudes J Dazard; Yana Sandlers; Stephanie K Doerner; Nathan A Berger; Henri Brunengraber
Journal:  BMC Syst Biol       Date:  2014-06-23
  5 in total

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