Polymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study.

2.50
Hdl Handle:
http://hdl.handle.net/10143/32572
Title:
Polymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study.
Authors:
Skjelbred, Camilla Furu; Sæbø, Mona; Wallin, Håkan; Nexø, Bjørn Andersen; Hagen, Per Christian; Lothe, Inger Marie Bowitz; Aase, Steinar; Johnson, Egil; Hansteen, Inger-Lise; Vogel, Ulla; Kure, Elin H
Citation:
BMC cancer 2006, 6:67

Full metadata record

DC FieldValue Language
dc.contributor.authorSkjelbred, Camilla Furu-
dc.contributor.authorSæbø, Mona-
dc.contributor.authorWallin, Håkan-
dc.contributor.authorNexø, Bjørn Andersen-
dc.contributor.authorHagen, Per Christian-
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.accessioned2008-07-21T11:07:16Z-
dc.date.available2008-07-21T11:07:16Z-
dc.date.issued2006-
dc.identifier.citationBMC cancer 2006, 6:67en
dc.identifier.issn1471-2407-
dc.identifier.pmid16542436-
dc.identifier.doi10.1186/1471-2407-6-67-
dc.identifier.urihttp://hdl.handle.net/10143/32572-
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.en
dc.language.isoenen
dc.subjectVDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk genetikk: 714en
dc.subjectVDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Onkologi: 762en
dc.subject.meshAdenomaen
dc.subject.meshAdulten
dc.subject.meshAgeden
dc.subject.meshAllelesen
dc.subject.meshCase-Control Studiesen
dc.subject.meshCohort Studiesen
dc.subject.meshColorectal Neoplasmsen
dc.subject.meshDNA-Binding Proteinsen
dc.subject.meshFemaleen
dc.subject.meshHumansen
dc.subject.meshMaleen
dc.subject.meshMiddle Ageden
dc.subject.meshPolymorphism, Geneticen
dc.subject.meshRisken
dc.subject.meshXeroderma Pigmentosum Group D Proteinen
dc.titlePolymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study.en
dc.typeJournal articleen
dc.typepeer revieweden
dc.contributor.departmentDepartment of Laboratory Medicine, Telemark Hospital, N-3710 Skien, Norway. camilla-furu.skjelbred@sthf.noen
dc.contributor.departmentUllevaal University Hospitalen
dc.identifier.journalBMC canceren
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