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Cancer Epidemiology Biomarkers & Prevention Vol. 14, 1619-1625, July 2005
© 2005 American Association for Cancer Research

Fruits, Vegetables, and hMLH1 Protein–Deficient and –Proficient Colon Cancer: The Netherlands Cohort Study

Petra A. Wark1, Matty P. Weijenberg2, Pieter van 't Veer1, Gerda van Wijhe1, Margreet Lüchtenborg2, Goos N.P. van Muijen4, Anton F.P.M. de Goeij3, R. Alexandra Goldbohm5 and Piet A. van den Brandt2

1 Division of Human Nutrition, Wageningen University, Wageningen, the Netherlands; 2 Nutrition and Toxicology Research Institute Maastricht (NUTRIM), Department of Epidemiology; 3 Research Institute Growth and Development (GROW), Department of Pathology, Maastricht University, the Netherlands; 4 Department of Pathology, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands; and 5 TNO Nutrition and Food Research, Zeist, the Netherlands

Requests for reprints: Matty P. Weijenberg, Department of Epidemiology, Maastricht University, P.O. Box 616, 6200 MD Maastricht, the Netherlands. E-mail: mp.weijenberg{at}epid.unimaas.nl

Background: Clinical and pathologic differences exist between colon carcinomas deficient and proficient in the mismatch repair protein hMLH1. Animal and in vitro studies suggest that fruits, vegetables, folate, and antioxidants are associated with colonic expression of mismatch repair genes.

Methods: Associations between consumption of fruits and vegetables and hMLH1 protein–deficient and –proficient colon cancer were evaluated in the Netherlands Cohort Study on diet and cancer using a case-cohort approach. A self-administered food frequency questionnaire was completed, in 1986, by 120,852 individuals ages 55 to 69 years. Using immunohistochemistry, hMLH1 protein expression was assessed in colon cancer tissue obtained from 441 patients who were identified over 7.3 years of follow-up excluding the initial 2.3 years. Incidence rate ratios (RR) were estimated for hMLH1 protein–deficient and –proficient colon cancer.

Results: hMLH1 protein expression was absent in 54 tumors (12.2%) and present in 387 tumors. Fruit consumption was associated with hMLH1 protein–deficient colon cancer [highest versus lowest tertile, RR, 0.46; 95% confidence interval (95% CI), 0.23-0.90; Ptrend = 0.029] but not with hMLH1 protein–proficient tumors (highest versus lowest tertile, RR, 1.03; 95% CI, 0.78-1.35; Ptrend = 0.81). Total consumption of vegetables was not associated with either type of tumor (hMLH1 protein deficient: RR, 0.86; 95% CI, 0.45-1.65; Ptrend = 0.67; hMLH1 protein proficient: RR, 0.94; 95% CI, 0.72-1.23; Ptrend = 0.72). No associations were observed for folate, fiber, antioxidants, or subgroups of vegetables.

Conclusion: These analyses indicate that an inverse association between consumption of fruits and colon cancer may be confined to the subgroup of tumors with a deficient mismatch repair system.




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Molecular Cancer Research Cancer Prevention Research
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Copyright © 2005 by the American Association for Cancer Research.