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Microenvironmental Snail1-induced immunosuppression promotes melanoma growth
Melanoma is an aggressive form of skin cancer due to its high metastatic abilities and resistance to therapies. Melanoma cells reside in a heterogeneous tumour microenvironment that acts as a crucial regulator of its progression. Snail1 is an epithelial-to-mesenchymal transition transcription factor...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473961/ https://www.ncbi.nlm.nih.gov/pubmed/37516803 http://dx.doi.org/10.1038/s41388-023-02793-5 |
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author | Arumi-Planas, Marta Rodriguez-Baena, Francisco Javier Cabello-Torres, Francisco Gracia, Francisco Lopez-Blau, Cristina Nieto, M. Angela Sanchez-Laorden, Berta |
author_facet | Arumi-Planas, Marta Rodriguez-Baena, Francisco Javier Cabello-Torres, Francisco Gracia, Francisco Lopez-Blau, Cristina Nieto, M. Angela Sanchez-Laorden, Berta |
author_sort | Arumi-Planas, Marta |
collection | PubMed |
description | Melanoma is an aggressive form of skin cancer due to its high metastatic abilities and resistance to therapies. Melanoma cells reside in a heterogeneous tumour microenvironment that acts as a crucial regulator of its progression. Snail1 is an epithelial-to-mesenchymal transition transcription factor expressed during development and reactivated in pathological situations including fibrosis and cancer. In this work, we show that Snail1 is activated in the melanoma microenvironment, particularly in fibroblasts. Analysis of mouse models that allow stromal Snail1 depletion and therapeutic Snail1 blockade indicate that targeting Snail1 in the tumour microenvironment decreases melanoma growth and lung metastatic burden, extending mice survival. Transcriptomic analysis of melanoma-associated fibroblasts and analysis of the tumours indicate that stromal Snail1 induces melanoma growth by promoting an immunosuppressive microenvironment and a decrease in anti-tumour immunity. This study unveils a novel role of Snail1 in melanoma biology and supports its potential as a therapeutic target. [Image: see text] |
format | Online Article Text |
id | pubmed-10473961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104739612023-09-03 Microenvironmental Snail1-induced immunosuppression promotes melanoma growth Arumi-Planas, Marta Rodriguez-Baena, Francisco Javier Cabello-Torres, Francisco Gracia, Francisco Lopez-Blau, Cristina Nieto, M. Angela Sanchez-Laorden, Berta Oncogene Article Melanoma is an aggressive form of skin cancer due to its high metastatic abilities and resistance to therapies. Melanoma cells reside in a heterogeneous tumour microenvironment that acts as a crucial regulator of its progression. Snail1 is an epithelial-to-mesenchymal transition transcription factor expressed during development and reactivated in pathological situations including fibrosis and cancer. In this work, we show that Snail1 is activated in the melanoma microenvironment, particularly in fibroblasts. Analysis of mouse models that allow stromal Snail1 depletion and therapeutic Snail1 blockade indicate that targeting Snail1 in the tumour microenvironment decreases melanoma growth and lung metastatic burden, extending mice survival. Transcriptomic analysis of melanoma-associated fibroblasts and analysis of the tumours indicate that stromal Snail1 induces melanoma growth by promoting an immunosuppressive microenvironment and a decrease in anti-tumour immunity. This study unveils a novel role of Snail1 in melanoma biology and supports its potential as a therapeutic target. [Image: see text] Nature Publishing Group UK 2023-07-29 2023 /pmc/articles/PMC10473961/ /pubmed/37516803 http://dx.doi.org/10.1038/s41388-023-02793-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Arumi-Planas, Marta Rodriguez-Baena, Francisco Javier Cabello-Torres, Francisco Gracia, Francisco Lopez-Blau, Cristina Nieto, M. Angela Sanchez-Laorden, Berta Microenvironmental Snail1-induced immunosuppression promotes melanoma growth |
title | Microenvironmental Snail1-induced immunosuppression promotes melanoma growth |
title_full | Microenvironmental Snail1-induced immunosuppression promotes melanoma growth |
title_fullStr | Microenvironmental Snail1-induced immunosuppression promotes melanoma growth |
title_full_unstemmed | Microenvironmental Snail1-induced immunosuppression promotes melanoma growth |
title_short | Microenvironmental Snail1-induced immunosuppression promotes melanoma growth |
title_sort | microenvironmental snail1-induced immunosuppression promotes melanoma growth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473961/ https://www.ncbi.nlm.nih.gov/pubmed/37516803 http://dx.doi.org/10.1038/s41388-023-02793-5 |
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