TY  - JOUR
AU  - Pardini, Barbara
AU  - Corrado, Alda
AU  - Paolicchi, Elisa
AU  - Cugliari, Giovanni
AU  - Berndt, Sonja I
AU  - Bezieau, Stephane
AU  - Bien, Stephanie A
AU  - Brenner, Hermann
AU  - Caan, Bette J
AU  - Campbell, Peter T
AU  - Casey, Graham
AU  - Chan, Andrew T
AU  - Chang-Claude, Jenny
AU  - Cotterchio, Michelle
AU  - Gala, Manish
AU  - Gallinger, Steven J
AU  - Haile, Robert W
AU  - Harrison, Tabitha A
AU  - Hayes, Richard B
AU  - Hoffmeister, Michael
AU  - Hopper, John L
AU  - Hsu, Li
AU  - Huyghe, Jeroen
AU  - Jenkins, Mark A
AU  - Le Marchand, Loic
AU  - Lin, Yi
AU  - Lindor, Noralane M
AU  - Nan, Hongmei
AU  - Newcomb, Polly A
AU  - Ogino, Shuji
AU  - Potter, John D
AU  - Schoen, Robert E
AU  - Slattery, Martha L
AU  - White, Emily
AU  - Vodickova, Ludmila
AU  - Vymetalkova, Veronika
AU  - Vodicka, Pavel
AU  - Gemignani, Federica
AU  - Peters, Ulrike
AU  - Naccarati, Alessio
AU  - Landi, Stefano
TI  - DNA repair and cancer in colon and rectum: novel players in genetic susceptibility.
JO  - International journal of cancer
VL  - 146
IS  - 2
SN  - 0020-7136
CY  - Bognor Regis
PB  - Wiley-Liss
M1  - DKFZ-2019-01631
SP  - 363-372
PY  - 2020
N1  - 146(2):363-372
AB  - Inter-individual differences in DNA repair systems may play a role in modulating the individual risk of developing colorectal cancer. To better ascertain the role of DNA repair gene polymorphisms on colon and rectal cancer risk individually, we evaluated 15,419 single nucleotide polymorphisms (SNPs) within 185 DNA repair genes using GWAS data from the Colon Cancer Family Registry (CCFR) and the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO), which included 8,178 colon cancer, 2,936 rectum cancer cases and 14,659 controls. Rs1800734 (in MLH1 gene) was associated with colon cancer risk (p-value=3.5x10-6 ) and rs2189517 (in RAD51B) with rectal cancer risk (p-value=5.7x10-6 ). The results had statistical significance close to the Bonferroni corrected p-value of 5.8x10-6 . Ninety-four SNPs were significantly associated with colorectal cancer risk after Binomial Sequential Goodness of Fit (BSGoF) procedure and confirmed the relevance of DNA mismatch repair (MMR) and homologous recombination pathways for colon and rectum cancer, respectively. Defects in MMR genes are known to be crucial for familial form of colorectal cancer but our findings suggest that specific genetic variations in MLH1 are important also in the individual predisposition to sporadic colon cancer. Other SNPs associated with the risk of colon cancer (e.g. rs16906252 in MGMT) were found to affect mRNA expression levels in colon transverse and therefore working as possible cis-eQTL suggesting possible mechanisms of carcinogenesis. This article is protected by copyright. All rights reserved.
LB  - PUB:(DE-HGF)16
C6  - pmid:31209889
DO  - DOI:10.1002/ijc.32516
UR  - https://inrepo02.dkfz.de/record/144081
ER  -