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Cooperative behaviour and phenotype plasticity evolve during melanoma progression

A major challenge for managing melanoma is its tumour heterogeneity based on individual co‐existing melanoma cell phenotypes. These phenotypes display variable responses to standard therapies, and they drive individual steps of melanoma progression; hence, understanding their behaviour is imperative...

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Autores principales: Rowling, Emily J., Miskolczi, Zsofia, Nagaraju, Raghavendar, Wilcock, Daniel J., Wang, Ping, Telfer, Brian, Li, Yaoyong, Lasheras-Otero, Irene, Redondo-Muñoz, Marta, Sharrocks, Andrew D., Arozarena, Imanol, Wellbrock, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496243/
https://www.ncbi.nlm.nih.gov/pubmed/32145051
http://dx.doi.org/10.1111/pcmr.12873
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author Rowling, Emily J.
Miskolczi, Zsofia
Nagaraju, Raghavendar
Wilcock, Daniel J.
Wang, Ping
Telfer, Brian
Li, Yaoyong
Lasheras-Otero, Irene
Redondo-Muñoz, Marta
Sharrocks, Andrew D.
Arozarena, Imanol
Wellbrock, Claudia
author_facet Rowling, Emily J.
Miskolczi, Zsofia
Nagaraju, Raghavendar
Wilcock, Daniel J.
Wang, Ping
Telfer, Brian
Li, Yaoyong
Lasheras-Otero, Irene
Redondo-Muñoz, Marta
Sharrocks, Andrew D.
Arozarena, Imanol
Wellbrock, Claudia
author_sort Rowling, Emily J.
collection PubMed
description A major challenge for managing melanoma is its tumour heterogeneity based on individual co‐existing melanoma cell phenotypes. These phenotypes display variable responses to standard therapies, and they drive individual steps of melanoma progression; hence, understanding their behaviour is imperative. Melanoma phenotypes are defined by distinct transcriptional states, which relate to different melanocyte lineage development phases, ranging from a mesenchymal, neural crest‐like to a proliferative, melanocytic phenotype. It is thought that adaptive phenotype plasticity based on transcriptional reprogramming drives melanoma progression, but at which stage individual phenotypes dominate and moreover, how they interact is poorly understood. We monitored melanocytic and mesenchymal phenotypes throughout melanoma progression and detected transcriptional reprogramming at different stages, with a gain in mesenchymal traits in circulating melanoma cells (CTCs) and proliferative features in metastatic tumours. Intriguingly, we found that distinct phenotype populations interact in a cooperative manner, which generates tumours of greater “fitness,” supports CTCs and expands organotropic cues in metastases. Fibronectin, expressed in mesenchymal cells, acts as key player in cooperativity and promotes survival of melanocytic cells. Our data reveal an important role for inter‐phenotype communications at various stages of disease progression, suggesting these communications could act as therapeutic target.
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spelling pubmed-74962432020-09-25 Cooperative behaviour and phenotype plasticity evolve during melanoma progression Rowling, Emily J. Miskolczi, Zsofia Nagaraju, Raghavendar Wilcock, Daniel J. Wang, Ping Telfer, Brian Li, Yaoyong Lasheras-Otero, Irene Redondo-Muñoz, Marta Sharrocks, Andrew D. Arozarena, Imanol Wellbrock, Claudia Pigment Cell Melanoma Res Original Articles A major challenge for managing melanoma is its tumour heterogeneity based on individual co‐existing melanoma cell phenotypes. These phenotypes display variable responses to standard therapies, and they drive individual steps of melanoma progression; hence, understanding their behaviour is imperative. Melanoma phenotypes are defined by distinct transcriptional states, which relate to different melanocyte lineage development phases, ranging from a mesenchymal, neural crest‐like to a proliferative, melanocytic phenotype. It is thought that adaptive phenotype plasticity based on transcriptional reprogramming drives melanoma progression, but at which stage individual phenotypes dominate and moreover, how they interact is poorly understood. We monitored melanocytic and mesenchymal phenotypes throughout melanoma progression and detected transcriptional reprogramming at different stages, with a gain in mesenchymal traits in circulating melanoma cells (CTCs) and proliferative features in metastatic tumours. Intriguingly, we found that distinct phenotype populations interact in a cooperative manner, which generates tumours of greater “fitness,” supports CTCs and expands organotropic cues in metastases. Fibronectin, expressed in mesenchymal cells, acts as key player in cooperativity and promotes survival of melanocytic cells. Our data reveal an important role for inter‐phenotype communications at various stages of disease progression, suggesting these communications could act as therapeutic target. John Wiley and Sons Inc. 2020-03-20 2020-09 /pmc/articles/PMC7496243/ /pubmed/32145051 http://dx.doi.org/10.1111/pcmr.12873 Text en © 2020 The Authors. Pigment Cell & Melanoma Research published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rowling, Emily J.
Miskolczi, Zsofia
Nagaraju, Raghavendar
Wilcock, Daniel J.
Wang, Ping
Telfer, Brian
Li, Yaoyong
Lasheras-Otero, Irene
Redondo-Muñoz, Marta
Sharrocks, Andrew D.
Arozarena, Imanol
Wellbrock, Claudia
Cooperative behaviour and phenotype plasticity evolve during melanoma progression
title Cooperative behaviour and phenotype plasticity evolve during melanoma progression
title_full Cooperative behaviour and phenotype plasticity evolve during melanoma progression
title_fullStr Cooperative behaviour and phenotype plasticity evolve during melanoma progression
title_full_unstemmed Cooperative behaviour and phenotype plasticity evolve during melanoma progression
title_short Cooperative behaviour and phenotype plasticity evolve during melanoma progression
title_sort cooperative behaviour and phenotype plasticity evolve during melanoma progression
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496243/
https://www.ncbi.nlm.nih.gov/pubmed/32145051
http://dx.doi.org/10.1111/pcmr.12873
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