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dc.contributor.authorChiorazzo, MG
dc.contributor.authorTunset, Hanna Maja
dc.contributor.authorPopov, AV
dc.contributor.authorJohansen, Berit
dc.contributor.authorMoestue, Siver Andreas
dc.contributor.authorDelikatny, EJ
dc.date.accessioned2019-04-24T12:15:26Z
dc.date.available2019-04-24T12:15:26Z
dc.date.created2018-12-10T09:01:29Z
dc.date.issued2019
dc.identifier.issn2045-2322
dc.identifier.urihttp://hdl.handle.net/11250/2595290
dc.description.abstractCytosolic phospholipase A2α (cPLA2α) has been shown to be elevated in breast cancer and is a potential biomarker in the differentiation of molecular sub-types. Using a cPLA2α activatable fluorophore, DDAO arachidonate, we explore its ability to function as a contrast agent in fluorescence-guided surgery. In cell lines ranging in cPLA2α expression and representing varying breast cancer sub-types, we show DDAO arachidonate activates with a high correlation to cPLA2α expression level. Using a control probe, DDAO palmitate, in addition to cPLA2α inhibition and genetic knockdown, we show that this activation is a result of cPLA2α activity. In mouse models, using an ex vivo tumor painting technique, we show that DDAO arachidonate activates to a high degree in basal-like versus luminal-like breast tumors and healthy mammary tissue. Finally, we show that using an in vivo model, orthotopic basal-like tumors give significantly high probe activation compared to healthy mammary fat pads and surrounding tissue. Together we conclude that cPLA2α activatable fluorophores such as DDAO arachidonate may serve as a useful contrast agent for the visualization of tumor margins in the fluorescence-guided surgery of basal-like breast cancer.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Naturenb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleDetection and differentiation of breast cancer sub-types using a cPLA2a activatable fluorophorenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.volume9nb_NO
dc.source.journalScientific Reportsnb_NO
dc.source.issue1nb_NO
dc.identifier.doi10.1038/s41598-019-41626-y
dc.identifier.cristin1640883
dc.relation.projectNorges forskningsråd: 239940nb_NO
dc.description.localcode© 2019 The Author(s). Open Access. This article is licensed under a Creative Commons Attribution 4.0 International Licensenb_NO
cristin.unitcode194,65,25,0
cristin.unitcode194,66,10,0
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.unitnameInstitutt for biologi
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedfalse
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal