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Association Between XRCC1 and XRCC3 Polymorphisms and Colorectal Cancer Risk: a Meta-analysis of 23 Case-control Studies

Overview
Journal Mol Biol Rep
Specialty Molecular Biology
Date 2012 Dec 29
PMID 23271134
Citations 12
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Abstract

Several potential functional polymorphisms in the DNA repair gene X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln (rs25487), Arg194Trp (rs1799782), Arg280His (rs25489) and X-ray repair cross-complementing group 3 (XRCC3) T241M (rs861539) have been implicated in colorectal cancer (CRC) risk, but the results are conflicting. Here, we performed a meta-analysis of 23 published case control datasets and assessed genetic heterogeneity between those datasets. All the case-control studies published from January 2000 to June 2012 on the association between those polymorphisms and CRC risk were identified by searching the electronic literature Medline. Statistical analysis was performed with the software programs Review Manager (version 4.2). For overall CRC, no significant association was observed, the pooled odds ratios for XRCC1 Arg399Gln, Arg194Trp, Arg280His, and XRCC3 T241M were 1.02 (95 % CI: 0.93, 1.12), 1.03 (95 % CI: 0.94, 1.14), 0.98 (95 % CI: 0.85, 1.13) and 1.03 (95 % CI: 0.85, 1.26), respectively. Furthermore, no significant association was observed in subgroup analyses based on ethnicity. The results suggested that these four SNPs evaluated are not associated with risk of CRC.

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References
1.
Stern M, Siegmund K, Corral R, Haile R . XRCC1 and XRCC3 polymorphisms and their role as effect modifiers of unsaturated fatty acids and antioxidant intake on colorectal adenomas risk. Cancer Epidemiol Biomarkers Prev. 2005; 14(3):609-15. DOI: 10.1158/1055-9965.EPI-04-0189. View

2.
Jin M, Chen K, Zhang Y, Zhang W, Liu B, Zhang Y . [Correlations of single nucleotide polymorphisms of DNA repair gene XRCC1 to risk of colorectal cancer]. Ai Zheng. 2007; 26(3):274-9. View

3.
Potter J, Slattery M, Bostick R, Gapstur S . Colon cancer: a review of the epidemiology. Epidemiol Rev. 1993; 15(2):499-545. DOI: 10.1093/oxfordjournals.epirev.a036132. View

4.
Duell E, Wiencke J, Cheng T, Varkonyi A, Zuo Z, Ashok T . Polymorphisms in the DNA repair genes XRCC1 and ERCC2 and biomarkers of DNA damage in human blood mononuclear cells. Carcinogenesis. 2000; 21(5):965-71. DOI: 10.1093/carcin/21.5.965. View

5.
Brevik A, Joshi A, Corral R, Onland-Moret N, Siegmund K, Le Marchand L . Polymorphisms in base excision repair genes as colorectal cancer risk factors and modifiers of the effect of diets high in red meat. Cancer Epidemiol Biomarkers Prev. 2010; 19(12):3167-73. PMC: 3058341. DOI: 10.1158/1055-9965.EPI-10-0606. View