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dc.contributor.authorVedeld, Hege M
dc.contributor.authorNesbakken, Arild
dc.contributor.authorLothe, Ragnhild A
dc.contributor.authorLind, Guro E
dc.date.accessioned2018-06-05T05:50:08Z
dc.date.available2018-06-05T05:50:08Z
dc.date.issued2018
dc.identifier.citationClinical Epigenetics. 2018 May 29;10(1):70
dc.identifier.urihttp://hdl.handle.net/10852/61776
dc.description.abstractWe have previously shown that aberrant promoter methylation of ZNF331 is a potential biomarker for colorectal cancer detection with high sensitivity (71%) and specificity (98%). This finding was recently confirmed by others, and it was additionally suggested that promoter methylation of ZNF331 was an independent prognostic biomarker for colorectal cancer (n = 146). In the current study, our initial colorectal cancer sample series was extended to include a total of 423 cancer tissue samples. Aberrant promoter methylation was found in 71% of the samples, thus repeatedly suggesting the biomarker potential of ZNF331 for detection of colorectal cancer. Furthermore, multivariate Cox’s analysis indicated a trend towards inferior overall survival for colorectal cancer patients with aberrant methylation of ZNF331.
dc.language.isoeng
dc.rightsThe Author(s); licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleRe-assessing ZNF331 as a DNA methylation biomarker for colorectal cancer
dc.typeJournal article
dc.date.updated2018-06-05T05:50:11Z
dc.creator.authorVedeld, Hege M
dc.creator.authorNesbakken, Arild
dc.creator.authorLothe, Ragnhild A
dc.creator.authorLind, Guro E
dc.identifier.doihttps://doi.org/10.1186/s13148-018-0503-2
dc.identifier.urnURN:NBN:no-64379
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/61776/1/13148_2018_Article_503.pdf
dc.type.versionPublishedVersion
cristin.articleid70


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