Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study

Detalhes bibliográficos
Autor(a) principal: Pópulo, H
Data de Publicação: 2021
Outros Autores: Domingues, B, Sampaio, C, Lopes, JM, Soares, P
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/152519
Resumo: Background: Melanoma accounts for only 1% of all skin malignant tumors; however, it is the deadliest form of skin cancer. Since 2011, FDA (Food and Drug Administration) approved several novel therapeutic strategies, such as MAPK pathway targeted therapies, to treat cutaneous melanoma patients. However, their improvements in overall survival were limited, due to the development of resistance. Methods: In this work, several combinations of therapies, including the metabolic mod-ulator DCA, were tested in melanoma cell lines, considering that MAPK and PI3K/AKT/ mTOR pathways are deregulated and interconnected in melanoma and that the presence of the Warburg effect in melanoma cells may influence the response to therapy. The effect of the treatments was assessed in the proliferation and survival of melanoma cell lines with different genetic profiles. Also, the possibility to overcome resistance to the treatment with vemurafenib was tested. Results: In general, higher decrease in cell viability and cell proliferation and increase in apoptosis were obtained after the combination treatments, comparing with single treatments, in all the studied cell lines. The combination of cobimetinib and everolimus appear to be the best treatment option. The BRAFV600E-vemurafenib resistant melanoma cell line showed to retain sensitivity to both everolimus and DCA. Discussion and Conclusion: Our results suggest that the combination of MAPK pathway inhibitors with mTOR pathway inhibitors and DCA should be considered as therapeutic options to treat melanoma patients, as the combinations potentiated the effects of each drug alone. In a cell line resistant to vemurafenib, we verified that combined MAPK inhibitors with inhibition of mTOR pathway and/or DCA metabolism modulation might constitute possible strategies in order to overcome resistance to MAPK inhibition.
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spelling Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro studyCobimetinibDCAEverolimusMelanomaMetabolismVemurafenibBackground: Melanoma accounts for only 1% of all skin malignant tumors; however, it is the deadliest form of skin cancer. Since 2011, FDA (Food and Drug Administration) approved several novel therapeutic strategies, such as MAPK pathway targeted therapies, to treat cutaneous melanoma patients. However, their improvements in overall survival were limited, due to the development of resistance. Methods: In this work, several combinations of therapies, including the metabolic mod-ulator DCA, were tested in melanoma cell lines, considering that MAPK and PI3K/AKT/ mTOR pathways are deregulated and interconnected in melanoma and that the presence of the Warburg effect in melanoma cells may influence the response to therapy. The effect of the treatments was assessed in the proliferation and survival of melanoma cell lines with different genetic profiles. Also, the possibility to overcome resistance to the treatment with vemurafenib was tested. Results: In general, higher decrease in cell viability and cell proliferation and increase in apoptosis were obtained after the combination treatments, comparing with single treatments, in all the studied cell lines. The combination of cobimetinib and everolimus appear to be the best treatment option. The BRAFV600E-vemurafenib resistant melanoma cell line showed to retain sensitivity to both everolimus and DCA. Discussion and Conclusion: Our results suggest that the combination of MAPK pathway inhibitors with mTOR pathway inhibitors and DCA should be considered as therapeutic options to treat melanoma patients, as the combinations potentiated the effects of each drug alone. In a cell line resistant to vemurafenib, we verified that combined MAPK inhibitors with inhibition of mTOR pathway and/or DCA metabolism modulation might constitute possible strategies in order to overcome resistance to MAPK inhibition.Dove Press20212021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/152519eng1179-145410.2147/JEP.S297831Pópulo, HDomingues, BSampaio, CLopes, JMSoares, Pinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T14:30:59Zoai:repositorio-aberto.up.pt:10216/152519Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:02:55.653374Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study
title Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study
spellingShingle Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study
Pópulo, H
Cobimetinib
DCA
Everolimus
Melanoma
Metabolism
Vemurafenib
title_short Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study
title_full Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study
title_fullStr Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study
title_full_unstemmed Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study
title_sort Combinatorial therapies to overcome braf/mek inhibitors resistance in melanoma cells: An in vitro study
author Pópulo, H
author_facet Pópulo, H
Domingues, B
Sampaio, C
Lopes, JM
Soares, P
author_role author
author2 Domingues, B
Sampaio, C
Lopes, JM
Soares, P
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Pópulo, H
Domingues, B
Sampaio, C
Lopes, JM
Soares, P
dc.subject.por.fl_str_mv Cobimetinib
DCA
Everolimus
Melanoma
Metabolism
Vemurafenib
topic Cobimetinib
DCA
Everolimus
Melanoma
Metabolism
Vemurafenib
description Background: Melanoma accounts for only 1% of all skin malignant tumors; however, it is the deadliest form of skin cancer. Since 2011, FDA (Food and Drug Administration) approved several novel therapeutic strategies, such as MAPK pathway targeted therapies, to treat cutaneous melanoma patients. However, their improvements in overall survival were limited, due to the development of resistance. Methods: In this work, several combinations of therapies, including the metabolic mod-ulator DCA, were tested in melanoma cell lines, considering that MAPK and PI3K/AKT/ mTOR pathways are deregulated and interconnected in melanoma and that the presence of the Warburg effect in melanoma cells may influence the response to therapy. The effect of the treatments was assessed in the proliferation and survival of melanoma cell lines with different genetic profiles. Also, the possibility to overcome resistance to the treatment with vemurafenib was tested. Results: In general, higher decrease in cell viability and cell proliferation and increase in apoptosis were obtained after the combination treatments, comparing with single treatments, in all the studied cell lines. The combination of cobimetinib and everolimus appear to be the best treatment option. The BRAFV600E-vemurafenib resistant melanoma cell line showed to retain sensitivity to both everolimus and DCA. Discussion and Conclusion: Our results suggest that the combination of MAPK pathway inhibitors with mTOR pathway inhibitors and DCA should be considered as therapeutic options to treat melanoma patients, as the combinations potentiated the effects of each drug alone. In a cell line resistant to vemurafenib, we verified that combined MAPK inhibitors with inhibition of mTOR pathway and/or DCA metabolism modulation might constitute possible strategies in order to overcome resistance to MAPK inhibition.
publishDate 2021
dc.date.none.fl_str_mv 2021
2021-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/10216/152519
url https://hdl.handle.net/10216/152519
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1179-1454
10.2147/JEP.S297831
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dc.publisher.none.fl_str_mv Dove Press
publisher.none.fl_str_mv Dove Press
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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