Environmental factors and colorectal tumor risk in individuals with hereditary nonpolyposis colorectal cancer

被引:61
作者
Diergaarde, Brenda
Braam, Hanneke
Vasen, Hans F.
Nagengast, Fokko M.
Van Muijen, Goos N. P.
Kok, Frans J.
Kampman, Ellen
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Pathol, Nijmegen, Netherlands
[2] Univ Wageningen & Res Ctr, Div Human Nutr, Wageningen, Netherlands
[3] Netherlands Fdn Detect Hereditary Tumors, Leiden, Netherlands
[4] Radboud Univ Nijmegen Med Ctr, Dept Gastroenterol, Nijmegen, Netherlands
关键词
D O I
10.1016/j.cgh.2007.02.019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Individuals with hereditary nonpolyposis colorectal cancer (HNPCC) are at increased risk for colorectal cancer. Environmental factors might play a role in HNPCC-associated carcinogenesis. The aim of this study was to gain insight into the effects of environmental factors on colorectat tumor risk in individuals with HNPCC. Methods: We examined associations between dietary factors, cigarette smoking, and HNPCC-associated colorectal tumors in a Dutch case-control study (145 cases, 103 tumor-free controls; all study participants were known or suspected carriers of a germline mutation in one of the DNA mismatch repair genes). We also assessed associations between the various environmental factors and occurrence of adenomatous polyposis coli (APC) mutations in HNPCC-associated polyps in a subset of the study population. Result: Fruit consumption was inversely associated with ever developing HNPCC-associated colorectal tumors (odds ratio [95% confidence interval] for highest vs lowest tertile, 0.4 [0.2- 0.9]; P-trend = .03); a borderline significant inverse association was observed for dietary fiber intake (0.5 [0.2-1.0]; P-trend = .06). Cigarette smoking seemed to increase the risk of HNPCC-associated colorectal. tumors. Truncating APC mutations were detected in 30 (37.5%) of the 80 available HNPCC-associated polyps; frameshift mutations were most common (73.3%). None of the evaluated environmental factors was distinctively associated with a specific APC status of the polyps. Conclusions: Our data suggest that fruit consumption and dietary fiber intake might decrease the risk of colorectal tumors in individuals with HNPCC, whereas cigarette smoking might increase the risk of HNPCC-associated colorectal tumors. The observed associations support the hypothesis that HNPCC-associated outcomes might be modified by environmental factors.
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页码:736 / 742
页数:7
相关论文
共 41 条
[1]   Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease [J].
Aaltonen, LA ;
Salovaara, R ;
Kristo, P ;
Canzian, F ;
Hemminki, A ;
Peltomäki, P ;
Chadwick, RB ;
Kääriäinen, H ;
Eskelinen, M ;
Järvinen, H ;
Mecklin, JP ;
de la Chapelle, A ;
Percesepe, A ;
Ahtola, H ;
Härkönen, N ;
Julkunen, R ;
Kangas, E ;
Ojala, S ;
Tulikoura, J ;
ValKamo, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (21) :1481-1487
[2]   β-Catenin and adenomatous polyposis coli (APC) mutations in adenomas from hereditary non-polyposis colorectal cancer patients [J].
Akiyama, Y ;
Nagasaki, H ;
Yagi, KO ;
Nomizu, T ;
Yuasa, Y .
CANCER LETTERS, 2000, 157 (02) :185-191
[4]   Dietary fibre in food and protection against colorectal cancer in the European Prospective Investigation into Cancer and Nutrition (EPIC): an observational study [J].
Bingham, SA ;
Day, NE ;
Luben, R ;
Ferrari, P ;
Slimani, N ;
Norat, T ;
Clavel-Chapelon, F ;
Kesse, E ;
Nieters, A ;
Boeing, H ;
Tjonneland, A ;
Overvad, K ;
Martinez, C ;
Dorronsoro, M ;
Gonzalez, CA ;
Key, TJ ;
Trichopoulou, A ;
Naska, A ;
Vineis, P ;
Tumino, R ;
Krogh, V ;
Bueno-de-Mesquita, HB ;
Peeters, PHM ;
Berglund, G ;
Hallmans, G ;
Lund, E ;
Skeie, G ;
Kaaks, R ;
Riboli, E .
LANCET, 2003, 361 (9368) :1496-1501
[5]   Mammalian DNA mismatch repair [J].
Buermeyer, AB ;
Deschênes, SM ;
Baker, SM ;
Liskay, RM .
ANNUAL REVIEW OF GENETICS, 1999, 33 :533-564
[6]  
BURKITT DP, 1971, CANCER, V28, P3, DOI 10.1002/1097-0142(197107)28:1<3::AID-CNCR2820280104>3.0.CO
[7]  
2-N
[8]   Surveillance for hereditary nonpolyposis colorectal cancer - A long-term study on 114 families [J].
Cappel, WHDTN ;
Nagengast, FM ;
Griffioen, G ;
Menko, FH ;
Taal, BG ;
Kleibeuker, JH ;
Vasen, HF .
DISEASES OF THE COLON & RECTUM, 2002, 45 (12) :1588-1594
[9]   The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas [J].
Cunningham, JM ;
Kim, CY ;
Christensen, ER ;
Tester, DJ ;
Parc, Y ;
Burgart, LJ ;
Halling, KC ;
McDonnell, SK ;
Schaid, DJ ;
Vockley, CW ;
Kubly, V ;
Nelson, H ;
Michels, VV ;
Thibodeau, SN .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) :780-790
[10]   Dietary factors and the occurrence of truncating APC mutations in sporadic colon carcinomas:: a Dutch population-based study [J].
Diergaarde, B ;
van Geloof, WL ;
van Muijen, GNP ;
Kok, FJ ;
Kampman, E .
CARCINOGENESIS, 2003, 24 (02) :283-290