Journal of Nutrition EB Program 2010 Abstracts

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© 2006 American Society for Nutrition J. Nutr. 136:3015-3021, December 2006


Nutrition and Disease

Dietary Folate and APC Mutations in Sporadic Colorectal Cancer1

Stefan de Vogel2,3,*, Manon van Engeland3, Margreet Lüchtenborg4,6, Adriaan P. de Bruïne3, Guido M. J. M. Roemen3, Marjolein H. F. M. Lentjes3, R. Alexandra Goldbohm5, Piet A. van den Brandt4, Anton F. P. M. de Goeij3 and Matty P. Weijenberg4

2 Research Institute Growth and Development (GROW), Department of Epidemiology; 3 Research Institute Growth and Development (GROW), Department of Pathology; and 4 Nutrition and Toxicology Research Institute Maastricht (NUTRIM), Department of Epidemiology, Maastricht University, Maastricht, The Netherlands and 5 TNO Quality of Life, Business Unit Food and Chemical Risk Analysis, Zeist, The Netherlands

* To whom correspondence should be addressed. E-mail: stefan.devogel{at}epid.unimaas.nl.

Folate deficiency has been associated with colorectal cancer risk and may be involved in colorectal carcinogenesis through increased chromosome instability, gene mutations, and aberrant DNA methylation. Within the Netherlands Cohort Study on diet and cancer, we investigated the associations between dietary folate intake and colorectal cancer risk with (APC+) and without (APC) truncating APC mutations, accounting for hMLH1 expression and K-ras mutations. In total, 528 cases and 4200 subcohort members were available for data analyses of the study cohort (n = 120,852) from a follow-up period between 2.3 and 7.3 y after baseline. Adjusted gender-specific incidence rate ratios (RR) over tertiles of folate intake were calculated in case-cohort analyses for colon and rectal cancer. Although relatively high folate intake was not associated with overall colorectal cancer risk, it reduced the risk of APCcolon tumors in men (RR 0.58, 95% CI 0.32–1.05, Ptrend = 0.06 for the highest vs. lowest tertile of folate intake). In contrast, it was positively associated with APC+ colon tumors in men (highest vs. lowest tertile: RR 2.77, 95% CI 1.29–5.95, Ptrend = 0.008) and was even stronger when the lack of hMLH1 expression and K-ras mutations were excluded (RR 3.99, 95% CI 1.43–11.14, Ptrend = 0.007). Such positive associations were not observed among women; nor was folate intake associated with rectal cancer when APC mutation status was taken into account. Relatively high folate consumption reduced the risk of APC colon tumors, but folate intake was positively associated with APC+ colon tumors among men. These opposite results may indicate that folate enhances colorectal carcinogenesis through a distinct APC mutated pathway.





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