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1Division of Applied Physiology, Exercise Science Department, 2Department of Biological Sciences, and 3Center for Colon Cancer Research, University of South Carolina, Columbia, South Carolina
Submitted 10 September 2007 ; accepted in final form 23 January 2008
Many epidemiological studies have demonstrated that level of exercise is associated with reduced colorectal cancer risk. Treadmill training can decrease ApcMin/+ mouse intestinal polyp number and size, but the mechanisms remain unclear. Understanding the molecular changes in the tumor following exercise training may provide insight on the mechanism by which exercise decreases ApcMin/+ mouse polyp formation and growth. The purpose of this study was to determine if exercise can modulate ApcMin/+ mouse intestinal polyp cellular signaling related to tumor formation and growth. Male ApcMin/+ mice were randomly assigned to control (n = 20) or exercise (n = 20) treatment groups. Exercised mice ran on a treadmill at a moderate intensity (18 m/min, 60 min, 6 days/wk, 5% grade) for 9 wk. Polyps from ApcMin/+ mice were used to quantify markers of polyp inflammation, apoptosis, and β-catenin signaling. Exercise decreased the number of macrophages in polyps by 35%. Related to apoptosis, exercise decreased the number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)-positive cells by 73% in all polyps. Bax protein expression in polyps was decreased 43% by exercise. β-Catenin phosphorylation was elevated 3.3-fold in polyps from exercised mice. Moderate-intensity exercise training alters cellular pathways in ApcMin/+ mouse polyps, and these changes may be related to the exercise-induced reduction in polyp formation and growth.
colon cancer; physical activity; inflammation; apoptosis; β-catenin
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