Polymorphisms in DNA repair genes XRCC1 and XRCC3, occupational exposure to arsenic and sunlight, and the risk of non-melanoma skin cancer in a European case-control study

X-ray repair cross-complementing group 1 (XRCC1) and group 3 (XRCC3) polymorphisms are relatively frequent in Caucasian populations and may have implications in skin cancer modulation. A few studies have evaluated their association with non-melanoma skin cancer (NMSC), but the results are inconsiste...

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Hauptverfasser: Surdu, Simona (VerfasserIn) , Fitzgerald, Edward F. (VerfasserIn) , Bloom, Michael S. (VerfasserIn) , Boscoe, Francis P. (VerfasserIn) , Carpenter, David O. (VerfasserIn) , Haase, Richard F. (VerfasserIn) , Gurzau, Eugen (VerfasserIn) , Rudnai, Peter (VerfasserIn) , Koppova, Kvetoslava (VerfasserIn) , Vahter, Marie (VerfasserIn) , Leonardi, Giovanni (VerfasserIn) , Goessler, Walter (VerfasserIn) , Kumar, Rajiv (VerfasserIn) , Fletcher, Tony (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 22 September 2014
In: Environmental research
Year: 2014, Jahrgang: 134, Pages: 382-389
ISSN:1096-0953
DOI:10.1016/j.envres.2014.08.020
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.envres.2014.08.020
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Verfasserangaben:Simona Surdu, Edward F. Fitzgerald, Michael S. Bloom, Francis P. Boscoe, David O. Carpenter, Richard F. Haase, Eugen Gurzau, Peter Rudnai, Kvetoslava Koppova, Marie Vahter, Giovanni Leonardi, Walter Goessler, Rajiv Kumar, Tony Fletcher

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245 1 0 |a Polymorphisms in DNA repair genes XRCC1 and XRCC3, occupational exposure to arsenic and sunlight, and the risk of non-melanoma skin cancer in a European case-control study  |c Simona Surdu, Edward F. Fitzgerald, Michael S. Bloom, Francis P. Boscoe, David O. Carpenter, Richard F. Haase, Eugen Gurzau, Peter Rudnai, Kvetoslava Koppova, Marie Vahter, Giovanni Leonardi, Walter Goessler, Rajiv Kumar, Tony Fletcher 
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520 |a X-ray repair cross-complementing group 1 (XRCC1) and group 3 (XRCC3) polymorphisms are relatively frequent in Caucasian populations and may have implications in skin cancer modulation. A few studies have evaluated their association with non-melanoma skin cancer (NMSC), but the results are inconsistent. In the current study, we aim to assess the impact of XRCC1 R399Q and XRCC3 T241M polymorphisms on the risk of NMSC associated with sunlight and arsenic exposure. Study participants consist of 618 new cases of NMSC and 527 hospital-based controls frequency matched on age, sex, and county of residence from Hungary, Romania, and Slovakia. Adjusted effects are estimated using multivariable logistic regression. The results indicate an increased risk of squamous cell carcinoma (SCC) for the homozygous variant genotype of XRCC1 R399Q (OR 2.53, 95% CI 1.14-5.65) and a protective effect against basal cell carcinoma (BCC) for the homozygous variant genotype of XRCC3 T241M (OR 0.61, 95% CI 0.41-0.92), compared with the respective homozygous common genotypes. Significant interactions are detected between XRCC3 T241M and sunlight exposure at work, and between XRCC3 T241M and exposure to arsenic in drinking water (p-value for interaction <0.10). In conclusion, the current study demonstrates that polymorphisms in XRCC genes may modify the associations between skin cancer risk and exposure to sunlight or arsenic. Given the high prevalence of genetic polymorphisms modifying the association between exposure to environmental carcinogens and NMSC, these results are of substantial relevance to public health. 
650 4 |a Aged 
650 4 |a Arsenic 
650 4 |a Case-Control Studies 
650 4 |a DNA Repair 
650 4 |a DNA repair polymorphisms 
650 4 |a Europe 
650 4 |a Exposure 
650 4 |a Female 
650 4 |a Humans 
650 4 |a Male 
650 4 |a Middle Aged 
650 4 |a Neoplasms, Radiation-Induced 
650 4 |a Non-melanoma skin cancer 
650 4 |a Occupational Exposure 
650 4 |a Polymorphism, Genetic 
650 4 |a Skin Neoplasms 
650 4 |a Sunlight 
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