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dc.contributor.authorToraskar, Jimita Prashant
dc.contributor.authorMagnussen, Synnøve
dc.contributor.authorChawla, Konika
dc.contributor.authorSvineng, Gunbjørg
dc.contributor.authorSteigedal, Tonje S.
dc.date.accessioned2019-01-05T09:07:56Z
dc.date.available2019-01-05T09:07:56Z
dc.date.created2018-11-06T13:03:34Z
dc.date.issued2018
dc.identifier.citationFEBS Open Bio. 2018, 1-10.nb_NO
dc.identifier.issn2211-5463
dc.identifier.urihttp://hdl.handle.net/11250/2579306
dc.description.abstractNephronectin (NPNT) is an extracellular matrix (ECM) protein involved in kidney development. We recently reported intracellular NPNT as a potential prognostic marker in breast cancer and that NPNT promotes metastasis in an integrin‐dependent manner. Here, we used reverse‐phase protein array (RPPA) to analyze NPNT‐triggered intracellular signaling in the 66cl4 mouse breast cancer cell line. The results showed that the integrin‐binding enhancer motif is important for the cellular effects upon NPNT interaction with its receptors, including phosphorylation of p38 mitogen‐activated protein kinase (MAPK). Furthermore, analysis using prediction tools suggests involvement of NPNT in promoting cell viability. In conclusion, our results indicate that NPNT, via its integrin‐binding motifs, promotes cell viability through phosphorylation of p38 MAPK.nb_NO
dc.language.isoengnb_NO
dc.publisherWiley Open Accessnb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleNephronectin mediates p38 MAPK‐induced cell viability via its integrin binding enhancer motifnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1-10nb_NO
dc.source.journalFEBS Open Bionb_NO
dc.identifier.doi10.1002/2211-5463.12544
dc.identifier.cristin1627492
dc.description.localcode© 2018 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution Licensenb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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