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Cancer Epidemiology Biomarkers & Prevention Vol. 14, 429-436, February 2005
© 2005 American Association for Cancer Research

Diet, Lifestyle, and Genomic Instability in the North Carolina Colon Cancer Study

Jessie A. Satia1,2,4, Temitope Keku3,4, Joseph A. Galanko4, Christopher Martin4, Ryan T. Doctolero5, Akihiro Tajima6, Robert S. Sandler3,4 and John M. Carethers5,6,7

1 Department of Global Epidemiology, Amgen, Inc., Thousand Oaks, California; 2 Department of Nutrition, Schools of Public Health and Medicine; 3 Division of Gastroenterology and Hematology, Department of Medicine, and 4 Center for Gastrointestinal Biology and Disease, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; 5 Veterans Affairs San Diego Healthcare System; 6 Department of Medicine and Moore's Comprehensive Cancer Center, University of California at San Diego; and 7 Veteran's Medical Research Foundation, San Diego, California

Requests for reprints: Jessie A. Satia, Department of Global Epidemiology, Amgen, Inc., One Amgen Center Drive, 24-1-C, Thousand Oaks, CA 91320. Phone: 805-313-4097; Fax: 805-498-5593. E-mail: jessie.satia{at}amgen.com

Objective: Microsatellite instability (MSI) is one form of genomic instability that occurs in 10% to 20% of sporadic colon tumors and almost all hereditary nonpolyposis colon cancers. However, little is known about how environmental factors (e.g., diet) may influence MSI in sporadic colon cancer.

Methods: We used data from a population-based case-control study in North Carolina (486 colon cancer cases and 1,048 controls) to examine associations of diet (total energy, macronutrients, micronutrients, and food groups) with MSI. In-person interviews elicited information on potential colon cancer risk factors, and a previously validated food frequency questionnaire adapted to include regional foods was used to assess diet over the year before diagnosis or interview date. MSI was classified as MSI-high (MSI-H) and MSI-low or microsatellite stable (MSI-L/MSS). Multivariate logistic regression models estimated energy-adjusted and non-energy-adjusted odds ratios (OR).

Results: Ten percent of the cases (n = 49) had MSI-H tumors (29% African American). The strongest associations between diet and MSI were observed in case-control comparisons: there was a robust inverse association between MSI-H status and ß-carotene [OR, 0.4; 95% confidence interval (95% CI), 0.2-0.9] and positive associations with energy-adjusted refined carbohydrates (OR, 2.2; 95% CI, 0.9-5.4) and non-energy-adjusted read meat intake (OR, 2.0; 95% CI, 0.9-4.2). Compared with controls, MSI-L/MSS tumors were statistically significantly associated with energy-adjusted vitamin C, vitamin E, calcium, dietary fiber, and dark green vegetables and positively associated with total energy intake (all Ps for trend < 0.05). In case-case comparisons, no dietary factors were significantly differently related to MSI-H compared with MSI-L/MSS tumors.

Conclusion: Refined carbohydrate and red meat consumption may promote development of MSI-H tumors, whereas ß-carotene may be associated with lower risk.




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Copyright © 2005 by the American Association for Cancer Research.