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.
机构:
Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Div Genet, Boston, MA 02115 USAHarvard Med Sch, Dept Genet, Boston, MA 02115 USA
机构:
Queen's University Belfast, Centre for Public Health, Institute of Clinical Sciences, Block B, Royal Victoria Hospital, Belfast, BT12 6BJ Northern Ireland, Grosvenor RoadQueen's University Belfast, Centre for Public Health, Institute of Clinical Sciences, Block B, Royal Victoria Hospital, Belfast, BT12 6BJ Northern Ireland, Grosvenor Road
机构:
Department of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States
College of Arts and Sciences, Boston University, Boston, MA 2215, United StatesDepartment of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States
Anil R Prasad
Shilpa Prasad
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Matrix Solutions Inc., Alberta T2R 0V2, CanadaDepartment of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States
Shilpa Prasad
Huy Nguyen
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机构:
Department of Cellular and Molecular Medicine, College of Medicine, University of Arizona, Tucson, AZ 85724, United StatesDepartment of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States
Huy Nguyen
Alexaner Facista
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Department of Cellular and Molecular Medicine, College of Medicine, University of Arizona, Tucson, AZ 85724, United StatesDepartment of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States
Alexaner Facista
Cristy Lewis
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Department of Cellular and Molecular Medicine, College of Medicine, University of Arizona, Tucson, AZ 85724, United StatesDepartment of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States
Cristy Lewis
Beryl Zaitlin
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Department of Pathology, College of Medicine, University of Arizona, Tucson, AZ 85724, United StatesDepartment of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States
Beryl Zaitlin
Harris Bernstein
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Department of Cellular and Molecular Medicine, College of Medicine, University of Arizona, Tucson, AZ 85724, United StatesDepartment of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States
Harris Bernstein
Carol Bernstein
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Department of Cellular and Molecular Medicine, College of Medicine, University of Arizona, Tucson, AZ 85724, United StatesDepartment of Pathology, Northwest Medical Center, Tucson, AZ 85741, United States