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Adaptive Responses as Mechanisms of Resistance to BRAF Inhibitors in Melanoma

The introduction of v-raf murine sarcoma viral oncogene homolog B (BRAF) inhibitors in melanoma patients with BRAF (V600E) mutations has demonstrated significant clinical benefits. However, rarely do tumours regress completely. Frequently, the reason for this is that therapies targeting specific onc...

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Detalles Bibliográficos
Autores principales: Saei, Azad, Eichhorn, Pieter Johan Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721815/
https://www.ncbi.nlm.nih.gov/pubmed/31416288
http://dx.doi.org/10.3390/cancers11081176
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author Saei, Azad
Eichhorn, Pieter Johan Adam
author_facet Saei, Azad
Eichhorn, Pieter Johan Adam
author_sort Saei, Azad
collection PubMed
description The introduction of v-raf murine sarcoma viral oncogene homolog B (BRAF) inhibitors in melanoma patients with BRAF (V600E) mutations has demonstrated significant clinical benefits. However, rarely do tumours regress completely. Frequently, the reason for this is that therapies targeting specific oncogenic mutations induce a number of intrinsic compensatory mechanisms, also known as adaptive responses or feedback loops, that enhance the pro-survival and pro-proliferative capacity of a proportion of the original tumour population, thereby resulting in tumour progression. In this review we will summarize the known adaptive responses that limit BRAF mutant therapy and discuss potential novel combinatorial therapies to overcome resistance.
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spelling pubmed-67218152019-09-10 Adaptive Responses as Mechanisms of Resistance to BRAF Inhibitors in Melanoma Saei, Azad Eichhorn, Pieter Johan Adam Cancers (Basel) Review The introduction of v-raf murine sarcoma viral oncogene homolog B (BRAF) inhibitors in melanoma patients with BRAF (V600E) mutations has demonstrated significant clinical benefits. However, rarely do tumours regress completely. Frequently, the reason for this is that therapies targeting specific oncogenic mutations induce a number of intrinsic compensatory mechanisms, also known as adaptive responses or feedback loops, that enhance the pro-survival and pro-proliferative capacity of a proportion of the original tumour population, thereby resulting in tumour progression. In this review we will summarize the known adaptive responses that limit BRAF mutant therapy and discuss potential novel combinatorial therapies to overcome resistance. MDPI 2019-08-14 /pmc/articles/PMC6721815/ /pubmed/31416288 http://dx.doi.org/10.3390/cancers11081176 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Saei, Azad
Eichhorn, Pieter Johan Adam
Adaptive Responses as Mechanisms of Resistance to BRAF Inhibitors in Melanoma
title Adaptive Responses as Mechanisms of Resistance to BRAF Inhibitors in Melanoma
title_full Adaptive Responses as Mechanisms of Resistance to BRAF Inhibitors in Melanoma
title_fullStr Adaptive Responses as Mechanisms of Resistance to BRAF Inhibitors in Melanoma
title_full_unstemmed Adaptive Responses as Mechanisms of Resistance to BRAF Inhibitors in Melanoma
title_short Adaptive Responses as Mechanisms of Resistance to BRAF Inhibitors in Melanoma
title_sort adaptive responses as mechanisms of resistance to braf inhibitors in melanoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721815/
https://www.ncbi.nlm.nih.gov/pubmed/31416288
http://dx.doi.org/10.3390/cancers11081176
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