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dc.contributor.authorSkjelbred, Camilla Furu
dc.contributor.authorSæbø, Mona
dc.contributor.authorWallin, Håkan
dc.contributor.authorNexø, Bjørn Andersen
dc.contributor.authorHagen, Per Chr.
dc.contributor.authorLothe, Inger Marie Bowitz
dc.contributor.authorAase, Steinar
dc.contributor.authorJohnson, Egil
dc.contributor.authorHansteen, Inger-Lise
dc.contributor.authorVogel, Ulla
dc.contributor.authorKure, Elin H.
dc.date.accessioned2007-06-26T11:25:46Z
dc.date.accessioned2017-04-19T13:40:21Z
dc.date.available2007-06-26T11:25:46Z
dc.date.available2017-04-19T13:40:21Z
dc.date.issued2006-03-16
dc.identifier.citationBMC Cancer 6(2006), No. 67
dc.identifier.issn1471-2407
dc.identifier.urihttp://hdl.handle.net/11250/2439250
dc.description.abstractBACKGROUND: Genetic polymorphisms in DNA repair genes may influence individual variation in DNA repair capacity, which may be associated with risk of developing cancer. For colorectal cancer the importance of mutations in mismatch repair genes has been extensively documented. Less is known about other DNA repair pathways in colorectal carcinogenesis. In this study we have focused on the XRCC1, XRCC3 and XPD genes, involved in base excision repair, homologous recombinational repair and nucleotide excision repair, respectively. METHODS: We used a case-control study design (157 carcinomas, 983 adenomas and 399 controls) to test the association between five polymorphisms in these DNA repair genes (XRCC1 Arg194Trp, Arg280His, Arg399Gln, XRCC3 Thr241Met and XPD Lys751Gln), and risk of colorectal adenomas and carcinomas in a Norwegian cohort. Odds ratio (OR) and 95% confidence interval (95% CI) were estimated by binary logistic regression model adjusting for age, gender, cigarette smoking and alcohol consumption. RESULTS: The XRCC1 280His allele was associated with an increased risk of adenomas (OR 2.30, 95% CI 1.19-4.46). The XRCC1 399Gln allele was associated with a reduction of risk of high-risk adenomas (OR 0.62, 95% CI 0.41-0.96). Carriers of the variant XPD 751Gln allele had an increased risk of low-risk adenomas (OR 1.40, 95% CI 1.03-1.89), while no association was found with risk of carcinomas. CONCLUSION: Our results suggest an increased risk for advanced colorectal neoplasia in individuals with the XRCC1 Arg280His polymorphism and a reduced risk associated with the XRCC1 Arg399Gln polymorphism. Interestingly, individuals with the XPD Lys751Gln polymorphism had an increased risk of low-risk adenomas. This may suggest a role in regression of adenomas.
dc.description.abstractForholdet mellom kolorektal neoplasi og mismatch repair gener (MMR) har vært undersøkt mye. Mindre er gjort i forhold til andre mekanismer for DNA reparasjon. Denne delstudien ser på mutasjoner i tre gener i sistnevnte kategori. Det ble bare funnet en assosiasjon mellom XPD 751Gln allele og adenomer, særlig lav-risiko adenomer. Manglende assosiasjon med høy-risoko adenomer og cancer kan ha sammenheng med utvalgsstørrelse. En annen mulighet er at XPD 751Gln kan spille en rolle i regresjon av adenomer (de fleste lav-risiko adenomer går i regresjon og utvikler seg ikke videre i retning av cancer).
dc.language.isoeng
dc.publisherBioMed Central
dc.subjectColorectal cancer
dc.subjectPolymorphisms
dc.subjectGenetics
dc.subjectAdenoma
dc.subjectColorectal Neoplasms
dc.subjectDNA-Binding Proteins
dc.titlePolymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study
dc.typeJournal article
dc.typePeer reviewed
dc.description.versionPublished version
dc.subject.nsi714
dc.subject.nsi762
dc.identifier.doihttp://dx.doi.org/10.1186/1471-2407-6-67


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