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dc.contributor.authorKiselev, Yury
dc.contributor.authorAndersen, Sigve
dc.contributor.authorJohannessen, Charles
dc.contributor.authorFjukstad, Bjørn
dc.contributor.authorOlsen, Karina Standahl
dc.contributor.authorStenvold, Helge
dc.contributor.authorAl-Saad, Samer
dc.contributor.authorDønnem, Tom
dc.contributor.authorRichardsen, Elin
dc.contributor.authorBremnes, Roy M.
dc.contributor.authorBusund, Lill-Tove
dc.date.accessioned2019-01-25T10:21:54Z
dc.date.accessioned2019-02-26T09:45:23Z
dc.date.available2019-01-25T10:21:54Z
dc.date.available2019-02-26T09:45:23Z
dc.date.issued2018-03-22
dc.identifier.citationKiselev Y, Andersen S, Johannessen C, Fjukstad B, Olsen KS, Stenvold S, Al-Saad SAS, Dønnem T, Richardsen ER, Bremnes RM, Busund LTRB. Transcription factor PAX6 as a novel prognostic factor and putative tumour suppressor in non-small cell lung cancer. Scientific Reports. 2018;8en
dc.identifier.issn2045-2322
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/10642/6677
dc.description.abstractLung cancer is the leading cause of cancer deaths. Novel predictive biomarkers are needed to improve treatment selection and more accurate prognostication. PAX6 is a transcription factor with a proposed tumour suppressor function. Immunohistochemical staining was performed on tissue microarrays from 335 non-small cell lung cancer (NSCLC) patients for PAX6. Multivariate analyses of clinico-pathological variables and disease-specific survival (DSS) was carried out, and phenotypic changes of two NSCLC cell lines with knockdown of PAX6 were characterized. While PAX6 expression was only associated with a trend of better disease-specific survival (DSS) (p = 0.10), the pN+ subgroup (N = 103) showed significant correlation between high PAX6 expression and longer DSS (p = 0.022). Median survival for pN + patients with high PAX6 expression was 127.4 months, versus 22.9 months for patients with low PAX6 expression. In NCI-H661 cells, knockdown of PAX6 strongly activated serum-stimulated migration. In NCI-H460 cells, PAX6 knockdown activated anchorage-independent growth. We did not observe any significant effect of PAX6 on proliferation in either of cell lines. Our findings strongly support the proposition of PAX6 as a valid and positive prognostic marker in NSCLC in node-positive patients. There is a need for further studies, which should provide mechanistical explanation for the role of PAX6 in NSCLC.en
dc.description.sponsorshipThis study was supported by a grant to Y.K. from Helse Nord (The Northern Norwegian Health Administration). The publication charges for this article have been funded by a grant from the publication fund of UiT The Arctic University of Norway.en
dc.language.isoenen
dc.publisherNature Researchen
dc.relation.ispartofseriesScientific Reports;Volume 8, Article number: 5059 (2018)
dc.rightsOpen Access: This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. © The Author(s) 2018en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectLung canceren
dc.subjectCancer deathsen
dc.subjectPredictive biomarkersen
dc.subjectPrognostic markersen
dc.subjectCancer treatmenten
dc.titleTranscription factor PAX6 as a novel prognostic factor and putative tumour suppressor in non-small cell lung canceren
dc.typeJournal articleen
dc.typePeer revieweden
dc.date.updated2019-01-25T10:21:54Z
dc.description.versionpublishedVersionen
dc.identifier.doihttps://dx.doi.org/10.1038/s41598-018-23417-z
dc.identifier.cristin1576102
dc.source.journalScientific Reports


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Open Access: This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. © The Author(s) 2018
Med mindre annet er angitt, så er denne innførselen lisensiert som Open Access: This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. © The Author(s) 2018