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dc.contributor.authorXu, CH
dc.contributor.authorWu, C
dc.contributor.authorXia, Y
dc.contributor.authorZhong, ZP
dc.contributor.authorLiu, Xiang
dc.contributor.authorXu, Jing
dc.contributor.authorCui, Fei
dc.contributor.authorChen, Bin
dc.contributor.authorRøe, Oluf Dimitri
dc.contributor.authorLi, AH
dc.contributor.authorChen, YJ
dc.date.accessioned2015-11-16T13:56:25Z
dc.date.accessioned2015-11-16T15:41:24Z
dc.date.available2015-11-16T13:56:25Z
dc.date.available2015-11-16T15:41:24Z
dc.date.issued2013
dc.identifier.citationPLoS ONE 2013, 8(8)nb_NO
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/11250/2360481
dc.description.abstractThe Wilms’ tumor suppressor gene (WT1) has been identified as an oncogene in many malignant diseases such as leukaemia, breast cancer, mesothelioma and lung cancer. However, the role of WT1 in non-small-cell lung cancer (NSCLC) carcinogenesis remains unclear. In this study, we compared WT1 mRNA levels in NSCLC tissues with paired corresponding adjacent tissues and identified significantly higher expression in NSCLC specimens. Cell proliferation of three NSCLC cell lines positively correlated with WT1 expression; moreover, these associations were identified in both cell lines and a xenograft mouse model. Furthermore, we demonstrated that up-regulation of Cyclin D1 and the phosphorylated retinoblastoma protein (p-pRb) was mechanistically related to WT1 accelerating cells to S-phase. In conclusion, our findings demonstrated that WT1 is an oncogene and promotes NSCLC cell proliferation by up-regulating Cyclin D1 and p-pRb expression.nb_NO
dc.language.isoengnb_NO
dc.publisherPublic Library of Sciencenb_NO
dc.titleWT1 Promotes Cell Proliferation in Non-Small Cell Lung Cancer Cell Lines Through Up-Regulating Cyclin D1 and p-pRb In Vitro and In Vivonb_NO
dc.typeJournal articlenb_NO
dc.typePeer revieweden_GB
dc.date.updated2015-11-16T13:56:25Z
dc.source.volume8nb_NO
dc.source.journalPLoS ONEnb_NO
dc.source.issue8nb_NO
dc.identifier.doi10.1371/journal.pone.0068837
dc.identifier.cristin1071524
dc.description.localcode© 2013 Xu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.nb_NO


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