Mouse models for unraveling the importance of diet in colon cancer prevention

被引:45
|
作者
Tammariello, Alexandra E. [3 ]
Milner, John A. [1 ,2 ]
机构
[1] NCI, Nutr Sci Res Grp, Canc Prevent Div, NIH,Hlth Serv, Rockville, MD 20892 USA
[2] NCI, Nutr Sci Res Grp, Canc Prevent Div, NIH,Human Serv, Rockville, MD 20892 USA
[3] Virginia Tech, Dept Human Nutr Foods & Exercise, Blacksburg, VA USA
关键词
Colorectal; Cancer; Diet; APC; Sulforaphane; Mouse; MULTIPLE INTESTINAL NEOPLASIA; FAMILIAL ADENOMATOUS POLYPOSIS; DNA MISMATCH REPAIR; COLORECTAL-CANCER; APC(MIN/+) MICE; VITAMIN-D; MIN MICE; KNOCKOUT MICE; BETA-CATENIN; FISH-OIL;
D O I
10.1016/j.jnutbio.2009.09.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diet and genetics are both considered important risk determinants for colorectal cancer, a leading cause of death worldwide. Several genetically engineered mouse models have been created, including the Apc(Min) mouse, to aid in the identification of key cancer related processes and to assist with the characterization of environmental factors, including the diet, which influence risk. Current research using these models provides evidence that several bioactive food components can inhibit genetically predisposed colorectal cancer, while others increase risk. Specifically, calorie restriction or increased exposure to n-3 fatty acids, sulforaphane, chafuroside, curcumin and dibenzoylmethane were reported protective. Total fat, calories and all-trans retinoic acid are associated with an increased risk. Unraveling the importance of specific dietary components in these models is complicated by the basal diet used, the quantity of test components provided and interactions among food components. Newer models are increasingly available to evaluate fundamental cellular processes, including DNA mismatch repair, immune function and inflammation as markers for colon cancer risk. Unfortunately, these models have been used infrequently to examine the influence of specific dietary components. The enhanced use of these models can shed mechanistic insights about the involvement of specific bioactive food and components and energy as determinants of colon cancer risk. However, the use of available mouse models to exactly represent processes important to human gastrointestinal cancers will remain a continued scientific challenge. Published by Elsevier Inc.
引用
收藏
页码:77 / 88
页数:12
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