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CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells.
Reigstad, Agathe; Herdlevær, Christina Frantzen; Rigg, Emma; Hoang, Tuyen; Bjørnstad, Ole Vidhammer; Aasen, Synnøve Nymark; Preis, Jasmin; Haan, Claude; Sundstrøm, Terje; Thorsen, Frits.
Affiliation
  • Reigstad A; Department of Biomedicine, University of Bergen, Bergen, Norway.
  • Herdlevær CF; Department of Biomedicine, University of Bergen, Bergen, Norway.
  • Rigg E; Department of Biomedicine, University of Bergen, Bergen, Norway.
  • Hoang T; Department of Biomedicine, University of Bergen, Bergen, Norway.
  • Bjørnstad OV; Department of Biomedicine, University of Bergen, Bergen, Norway.
  • Aasen SN; Department of Biomedicine, University of Bergen, Bergen, Norway.
  • Preis J; Faculty of Health and Social Sciences, Western Norway University of Applied Sciences, Bergen, Norway.
  • Haan C; Department of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
  • Sundstrøm T; Department of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
  • Thorsen F; Department of Neurosurgery, Haukeland University Hospital, Bergen, Norway.
PLoS One ; 17(9): e0273711, 2022.
Article in En | MEDLINE | ID: mdl-36084109
ABSTRACT
Melanomas 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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Melanoma Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2022 Document type: Article Affiliation country: Noruega

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Melanoma Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2022 Document type: Article Affiliation country: Noruega