XRCC1 Gene Polymorphism, Diet and Risk of Colorectal Cancer in Thailand

被引:8
作者
Poomphakwaen, Kirati [1 ]
Promthet, Supannee [1 ]
Suwanrungruang, Krittika [2 ]
Chopjitt, Peechanika [3 ]
Songserm, Nopparat [5 ]
Wiangnon, Surapon [4 ]
机构
[1] Khon Kaen Univ, Fac Publ Hlth, Dept Epidemiol, Khon Kaen, Thailand
[2] Khon Kaen Univ, Fac Med, Canc Unit, Khon Kaen, Thailand
[3] Khon Kaen Univ, Fac Med, Dept Microbiol, Khon Kaen, Thailand
[4] Khon Kaen Univ, Fac Med, Dept Paediat, Khon Kaen, Thailand
[5] Ubon Ratchathani Rajabhat Univ, Fac Publ Hlth, Dept Community Hlth, Ubon Ratchathani, Thailand
关键词
XRCC1; polymorphism; risk factors; colorectal cancer; Thailand; EXCISION-REPAIR GENES; MEAT CONSUMPTION; ARG399GLN POLYMORPHISM; ALCOHOL-CONSUMPTION; CIGARETTE-SMOKING; FISH CONSUMPTION; METAANALYSIS; ASSOCIATION; PATTERNS; CARCINOMA;
D O I
10.7314/APJCP.2014.15.17.7479
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Colorectal cancer (CRC) is one of the most common cancers worldwide. This study aimed to investigate the interaction between the presence of a polymorphism of the XRCC1 gene and known risk factors for colorectal cancer in Thailand. Materials and Methods: A hospital-based case-control study was conducted in Thailand. The participants were 230 histologically confirmed new cases and 230 controls matched by sex and age and recruited from the same hospital. Information about demographic characteristics, life style, and dietary habits was collected using structured interviews, and blood samples were taken which were used for the detection of a homozygous and heterozygous polymorphisms of XRCC1. Associations were assessed using multiple conditional logistic regression. Results: In the univariate analysis, factors found to be significantly associated with an increased risk for CRC were the presence of the XRCC1 AA homozygote (OR=4.95; 95% CI: 1.99-12.3), a first degree family history of cancer (OR=1.74; 95% CI: 1.18-2.58), and a high frequency of pork consumption (OR=1.49; 95% CI: 1.00-2.21). Intakes of fish fruit and vegetables appeared to be protective factors, but the associations were not statistically significant. In the multivariate analysis only the XRCC1 AA homozygote polymorphism and a family history of cancer emerged as risk factors (OR=4.96; 95% CI: 1.90-12.95 and OR=1.80; 95% CI: 1.18-2.72, respectively). Conclusions: While the XRCC1 AA homozygote and a family history of cancer were found to be associated with an increased risk of CRC, none of the dietary intake variables were clearly identified as risk or protective factors. There is a need for further research to determine the reasons for this.
引用
收藏
页码:7479 / 7486
页数:8
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