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dc.contributor.authorToraskar, Jimita Prashant
dc.contributor.authorNorvoll Magnussen, Synnøve
dc.contributor.authorHagen, Lars
dc.contributor.authorSharma, Animesh
dc.contributor.authorHoang, Linh
dc.contributor.authorBjørkøy, Geir
dc.contributor.authorSvineng, Gunbjørg
dc.contributor.authorSteigedal, Tonje S.
dc.date.accessioned2020-02-05T09:23:10Z
dc.date.available2020-02-05T09:23:10Z
dc.date.created2019-03-13T13:24:35Z
dc.date.issued2019
dc.identifier.citationJournal of Proteome Research. 2019, 18 (3), 1237-1247.nb_NO
dc.identifier.issn1535-3893
dc.identifier.urihttp://hdl.handle.net/11250/2639720
dc.description.abstractExtracellular vesicles are emerging as biomarkers in breast cancer. Our recent report suggested that an intracellular granular staining pattern of the extracellular matrix protein nephronectin (NPNT) in breast tumor sections correlated with a poor prognosis. Furthermore, the results showed that NPNT is localized in extracellular vesicles derived from mouse breast cancer cells. In this study, we performed proteomic analysis that revealed that several proteins, including tumor-promoting molecules, are differentially expressed in the cargo of small extracellular vesicles (sEVs) derived from NPNT-expressing mouse breast cancer cells. We also identified three different forms of NPNT at 80, 60, and 20 kDa. We report that the native form of NPNT at 60 kDa becomes further glycosylated and is detected as the 80 kDa NPNT, which may be processed by matrix metalloproteinases to a shorter form of around 20 kDa, which has not previously been described. Although both 80 and 20 kDa NPNT are detected in sEVs derived from breast cancer cells, the 20 kDa form of NPNT is concentrated in sEVs. In summary, we show that a novel truncated form of NPNT is found in sEVs derived from breast cancer cells.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.relation.urihttps://pubs.acs.org/doi/ipdf/10.1021/acs.jproteome.8b00859
dc.titleA Novel Truncated Form of Nephronectin Is Present in Small Extracellular Vesicles Isolated from 66cl4 Cellsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1237-1247nb_NO
dc.source.volume18nb_NO
dc.source.journalJournal of Proteome Researchnb_NO
dc.source.issue3nb_NO
dc.identifier.doi10.1021/acs.jproteome.8b00859
dc.identifier.cristin1684472
dc.relation.projectNotur/NorStore: NS9036Knb_NO
dc.description.localcodeThis is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.nb_NO
cristin.unitcode194,65,15,0
cristin.unitcode194,66,40,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameInstitutt for bioingeniørfag
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.fulltextoriginal
cristin.qualitycode2


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