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CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells

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 docu...

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Autores principales: Reigstad, Agathe, Herdlevær, Christina Frantzen, Rigg, Emma, Hoang, Tuyen, Bjørnstad, Ole Vidhammer, Aasen, Synnøve Nymark, Preis, Jasmin, Haan, Claude, Sundstrøm, Terje, Thorsen, Frits
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462752/
https://www.ncbi.nlm.nih.gov/pubmed/36084109
http://dx.doi.org/10.1371/journal.pone.0273711
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author Reigstad, Agathe
Herdlevær, Christina Frantzen
Rigg, Emma
Hoang, Tuyen
Bjørnstad, Ole Vidhammer
Aasen, Synnøve Nymark
Preis, Jasmin
Haan, Claude
Sundstrøm, Terje
Thorsen, Frits
author_facet Reigstad, Agathe
Herdlevær, Christina Frantzen
Rigg, Emma
Hoang, Tuyen
Bjørnstad, Ole Vidhammer
Aasen, Synnøve Nymark
Preis, Jasmin
Haan, Claude
Sundstrøm, Terje
Thorsen, Frits
author_sort Reigstad, Agathe
collection PubMed
description 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 IC(50) 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.
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spelling pubmed-94627522022-09-10 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 PLoS One Research Article 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 IC(50) 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. Public Library of Science 2022-09-09 /pmc/articles/PMC9462752/ /pubmed/36084109 http://dx.doi.org/10.1371/journal.pone.0273711 Text en © 2022 Reigstad et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Reigstad, Agathe
Herdlevær, Christina Frantzen
Rigg, Emma
Hoang, Tuyen
Bjørnstad, Ole Vidhammer
Aasen, Synnøve Nymark
Preis, Jasmin
Haan, Claude
Sundstrøm, Terje
Thorsen, Frits
CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells
title CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells
title_full CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells
title_fullStr CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells
title_full_unstemmed CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells
title_short CCT196969 effectively inhibits growth and survival of melanoma brain metastasis cells
title_sort cct196969 effectively inhibits growth and survival of melanoma brain metastasis cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462752/
https://www.ncbi.nlm.nih.gov/pubmed/36084109
http://dx.doi.org/10.1371/journal.pone.0273711
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