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Cytoskeletal Remodelling as an Achilles’ Heel for Therapy Resistance in Melanoma

Melanoma is an aggressive skin cancer with a poor prognosis when diagnosed late. MAPK-targeted therapies and immune checkpoint blockers benefit a subset of melanoma patients; however, acquired therapy resistance inevitably arises within a year. In addition, some patients display intrinsic (primary)...

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Detalles Bibliográficos
Autores principales: Barreno, Adrian, Orgaz, Jose L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834185/
https://www.ncbi.nlm.nih.gov/pubmed/35159327
http://dx.doi.org/10.3390/cells11030518
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author Barreno, Adrian
Orgaz, Jose L.
author_facet Barreno, Adrian
Orgaz, Jose L.
author_sort Barreno, Adrian
collection PubMed
description Melanoma is an aggressive skin cancer with a poor prognosis when diagnosed late. MAPK-targeted therapies and immune checkpoint blockers benefit a subset of melanoma patients; however, acquired therapy resistance inevitably arises within a year. In addition, some patients display intrinsic (primary) resistance and never respond to therapy. There is mounting evidence that resistant cells adapt to therapy through the rewiring of cytoskeleton regulators, leading to a profound remodelling of the actomyosin cytoskeleton. Importantly, this renders therapy-resistant cells highly dependent on cytoskeletal signalling pathways for sustaining their survival under drug pressure, which becomes a vulnerability that can be exploited therapeutically. Here, we discuss the current knowledge on cytoskeletal pathways involved in mainly targeted therapy resistance and future avenues, as well as potential clinical interventions.
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spelling pubmed-88341852022-02-12 Cytoskeletal Remodelling as an Achilles’ Heel for Therapy Resistance in Melanoma Barreno, Adrian Orgaz, Jose L. Cells Review Melanoma is an aggressive skin cancer with a poor prognosis when diagnosed late. MAPK-targeted therapies and immune checkpoint blockers benefit a subset of melanoma patients; however, acquired therapy resistance inevitably arises within a year. In addition, some patients display intrinsic (primary) resistance and never respond to therapy. There is mounting evidence that resistant cells adapt to therapy through the rewiring of cytoskeleton regulators, leading to a profound remodelling of the actomyosin cytoskeleton. Importantly, this renders therapy-resistant cells highly dependent on cytoskeletal signalling pathways for sustaining their survival under drug pressure, which becomes a vulnerability that can be exploited therapeutically. Here, we discuss the current knowledge on cytoskeletal pathways involved in mainly targeted therapy resistance and future avenues, as well as potential clinical interventions. MDPI 2022-02-02 /pmc/articles/PMC8834185/ /pubmed/35159327 http://dx.doi.org/10.3390/cells11030518 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Barreno, Adrian
Orgaz, Jose L.
Cytoskeletal Remodelling as an Achilles’ Heel for Therapy Resistance in Melanoma
title Cytoskeletal Remodelling as an Achilles’ Heel for Therapy Resistance in Melanoma
title_full Cytoskeletal Remodelling as an Achilles’ Heel for Therapy Resistance in Melanoma
title_fullStr Cytoskeletal Remodelling as an Achilles’ Heel for Therapy Resistance in Melanoma
title_full_unstemmed Cytoskeletal Remodelling as an Achilles’ Heel for Therapy Resistance in Melanoma
title_short Cytoskeletal Remodelling as an Achilles’ Heel for Therapy Resistance in Melanoma
title_sort cytoskeletal remodelling as an achilles’ heel for therapy resistance in melanoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834185/
https://www.ncbi.nlm.nih.gov/pubmed/35159327
http://dx.doi.org/10.3390/cells11030518
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