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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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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. |
format | Online Article Text |
id | pubmed-9462752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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