Dietary folate intake and K-ras mutations in sporadic colon and rectal cancer in The Netherlands Cohort Study

被引:23
作者
Brink, M
Weijenberg, MP
de Goeij, AFPM
Roemen, GMJM
Lentjes, MHFM
de Bruïne, AP
van Engeland, M
Goldbohm, RA
van den Brandt, PA
机构
[1] Maastricht Univ, NUTRIM, Dept Epidemiol, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Res Inst Growth & Dev, GROW, Dept Pathol, NL-6200 MD Maastricht, Netherlands
[3] TNO, Nutr & Food Res, NL-3700 AJ Zeist, Netherlands
关键词
men; women; transversion; wild-type;
D O I
10.1002/ijc.20775
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We studied the association between dietary folate and specific K-ras mutations in colon and rectal cancer in The Netherlands Cohort Study on diet and cancer. After 7.3 years of follow-up, 448 colon and 160 rectal cancer patients and 3,048 sub-cohort members (55-69 years at baseline) were available for data analyses. Mutation analysis of the K-ras gene was carried out on all archival adenocarcinoma specimens. Case-cohort analyses were used to compute adjusted incidence rate ratios (RR) and 95% confidence intervals (Cl) for colon and rectal cancer overall and for K-ras mutation status subgroups according to 100 mug/day increased intake in dietary folate. Dietary folate intake was not significantly associated with colon cancer risk for men or women, neither overall nor with K-ras mutation status. For rectal cancer, folate intake was associated with a decreased disease risk in men and was most pronounced for K-ras mutated tumors, whereas an increased association was observed for women. Regarding the K-ras mutation status in women, an increased association was observed for both wild-type and mutated K-ras tumors. Specifically, folate intake was associated with an increased risk of G>T and G>C transversions in rectal tumors (RR = 2.69, 95% CI 1.43-5.09), but inversely associated with G>A transitions (RR 0.08, 95% CI = 0.01-0.53). Our data suggest that the effect of folate on rectal cancer risk is different for men and women and depends on the K-ras mutation status of the tumor. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:824 / 830
页数:7
相关论文
共 32 条
[1]  
[Anonymous], 1986, NEVO TABLE DUTCH FOO
[2]   Analysis of case-cohort designs [J].
Barlow, WE ;
Ichikawa, L ;
Rosner, D ;
Izumi, S .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1999, 52 (12) :1165-1172
[3]  
Bautista D, 1997, CANCER EPIDEM BIOMAR, V6, P57
[4]   PREVALENCE OF RAS GENE-MUTATIONS IN HUMAN COLORECTAL CANCERS [J].
BOS, JL ;
FEARON, ER ;
HAMILTON, SR ;
VERLAANDEVRIES, M ;
VANBOOM, JH ;
VANDEREB, AJ ;
VOGELSTEIN, B .
NATURE, 1987, 327 (6120) :293-297
[5]   K-RAS MUTATION IN COLORECTAL-CANCER - RELATIONS TO PATIENT AGE, SEX AND TUMOR LOCATION [J].
BREIVIK, J ;
MELING, GI ;
SPURKLAND, A ;
ROGNUM, TO ;
GAUDERNACK, G .
BRITISH JOURNAL OF CANCER, 1994, 69 (02) :367-371
[6]   K-ras oncogene mutations in sporadic colorectal cancer in The Netherlands Cohort Study [J].
Brink, M ;
de Goeij, AFPM ;
Weijenberg, MP ;
Roemen, GMJM ;
Lentjes, MHFM ;
Pachen, MMM ;
Smits, KM ;
de Bruïne, AP ;
Goldbohm, RA ;
van den Brandt, PA .
CARCINOGENESIS, 2003, 24 (04) :703-710
[7]  
DORANT E, 1994, CANCER RES, V54, P6148
[8]  
Esteller M, 2000, CANCER RES, V60, P2368
[9]   Commentary: Colon cancer, folate and genetic status [J].
Fallon, UB .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2003, 32 (01) :67-70
[10]   Epidemiologic studies of folate and colorectal neoplasia: a review [J].
Giovannucci, E .
JOURNAL OF NUTRITION, 2002, 132 (08) :2350S-2355S