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dc.contributor.authorReigstad, Agathe
dc.contributor.authorHerdlevær, Christina Frantzen
dc.contributor.authorRigg, Emma Kayleigh
dc.contributor.authorHoang, Tuyen
dc.contributor.authorBjørnstad, Ole Vidhammer
dc.contributor.authorAasen, Synnøve Nymark
dc.contributor.authorPreis, Jasmin
dc.contributor.authorHaan, Claude
dc.contributor.authorSundstrøm, Terje
dc.contributor.authorThorsen, Frits
dc.date.accessioned2022-10-28T12:30:23Z
dc.date.available2022-10-28T12:30:23Z
dc.date.created2022-10-19T10:06:42Z
dc.date.issued2022
dc.identifier.issn1932-6203
dc.identifier.urihttps://hdl.handle.net/11250/3028892
dc.description.abstractMelanomas frequently metastasize to the brain. Despite recent progress in the treatment of melanoma brain metastasis, therapy resistance and relapse of disease remain unsolved challenges. CCT196969 is a SRC family kinase (SFK) and Raf proto-oncogene, serine/threonine kinase (RAF) inhibitor with documented effects in primary melanoma cell lines in vitro and in vivo. Using in vitro cell line assays, we studied the effects of CCT196969 in multiple melanoma brain metastasis cell lines. The drug effectively inhibited proliferation, migration, and survival in all examined cell lines, with viability IC50 doses in the range of 0.18–2.6 μM. Western blot analysis showed decreased expression of p-ERK, p-MEK, p-STAT3 and STAT3 upon CCT196969 treatment. Furthermore, CCT196969 inhibited viability in two B-Raf Proto-Oncogene (BRAF) inhibitor resistant metastatic melanoma cell lines. Further in vivo studies should be performed to determine the treatment potential of CCT196969 in patients with treatment-naïve and resistant melanoma brain metastasis.en_US
dc.language.isoengen_US
dc.publisherPLOSen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleCCT196969 effectively inhibits growth and survival of melanoma brain metastasis cellsen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.source.articlenumbere0273711en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1371/journal.pone.0273711
dc.identifier.cristin2062626
dc.source.journalPLOS ONEen_US
dc.identifier.citationPLOS ONE. 2022, 17 (9), e0273711.en_US
dc.source.volume17en_US
dc.source.issue9en_US


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