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dc.contributor.authorHansen, Rikke
dc.contributor.authorSæbø, Mona
dc.contributor.authorSkjelbred, Camilla Furu
dc.contributor.authorNexø, Bjørn Andersen
dc.contributor.authorHagen, Per Chr.
dc.contributor.authorBock, Günther
dc.contributor.authorLothe, Inger Marie Bowitz
dc.contributor.authorJohnson, Egil
dc.contributor.authorAase, Steinar
dc.contributor.authorHansteen, Inger-Lise
dc.contributor.authorVogel, Ulla
dc.contributor.authorKure, Elin H.
dc.date.accessioned2007-06-26T11:49:14Z
dc.date.accessioned2017-04-19T13:40:20Z
dc.date.available2007-06-26T11:49:14Z
dc.date.available2017-04-19T13:40:20Z
dc.date.issued2005
dc.identifier.citationCancer letters 229(2005), No. 1, p. 85-91
dc.identifier.issn0304-3835
dc.identifier.urihttp://hdl.handle.net/11250/2439248
dc.description.abstractLittle is known about genetic risk factors for colorectal cancer. We assessed the association between polymorphisms in two genes involved in DNA repair of oxidative stress, GPX and OGG1, and risk of colorectal carcinoma or adenomas. We studied 166 cases with adenocarcinoma, 974 with adenomas and 397 controls recruited from the Norwegian cohort NORCCAP. No associations were found between the polymorphism GPX Pro198Leu and risk of colorectal adenomas or carcinomas. Carriers of the variant allele OGG1 Ser326Cys polymorphism had a lowered risk of colorectal cancer, OR=0.56 (95% confidence interval 0.33-0.95), while no association were found with risk of adenomas. This indicates that a low repair capacity of oxidative DNA damage may not be a risk factor for development of colorectal adenomas or carcinoma.
dc.description.abstractOksidative prosesser kan skade DNA. Denne artikkelen tar for seg varianter (polymorfismer) av to gener (GPX og OGG1) som er involvert i DNA reparasjon ved oksidativt stress. Av disse genene var det bare en variant av OGG1 som var assosiert med en redusert risiko for kolorektal cancer, men ingen assosiasjon med adenomer enten disse hadde lav- eller høygradig dysplasi. GPX viste ingen assosiasjon hverken med cancer eller adenomer. En mulig forklaring er at redusert forsvar mot oksidativt stress ikke utgjør noen vesentlig risiko for utvikling av adenomer og cancer i tykktarm/endetarm.
dc.language.isoeng
dc.publisherElsevier
dc.subjectColorectal cancer
dc.subjectDysplasia
dc.subjectOxidative stress
dc.subjectPopulation based
dc.subjectAdenomas
dc.titleGPX Pro198Leu and OGG1 Ser326Cys polymorphisms and risk of development of colorectal adenomas and colorectal cancer
dc.typeJournal article
dc.typePeer reviewed
dc.description.versionAccepted version
dc.subject.nsi714
dc.subject.nsi762
dc.identifier.doihttp://dx.doi.org/10.1016/j.canlet.2005.04.019


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