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Epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts
Carcinoma-associated fibroblasts (CAF) mediate the onset of a proinvasive tumour microenvironment. The proinflammatory cytokine LIF reprograms fibroblasts into a proinvasive phenotype, which promotes extracellular matrix remodelling and collective invasion of cancer cells. Here we unveil that exposu...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682161/ https://www.ncbi.nlm.nih.gov/pubmed/26667266 http://dx.doi.org/10.1038/ncomms10204 |
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author | Albrengues, Jean Bertero, Thomas Grasset, Eloise Bonan, Stephanie Maiel, Majdi Bourget, Isabelle Philippe, Claude Herraiz Serrano, Cecilia Benamar, Samia Croce, Olivier Sanz-Moreno, Victoria Meneguzzi, Guerrino Feral, Chloe C. Cristofari, Gael Gaggioli, Cedric |
author_facet | Albrengues, Jean Bertero, Thomas Grasset, Eloise Bonan, Stephanie Maiel, Majdi Bourget, Isabelle Philippe, Claude Herraiz Serrano, Cecilia Benamar, Samia Croce, Olivier Sanz-Moreno, Victoria Meneguzzi, Guerrino Feral, Chloe C. Cristofari, Gael Gaggioli, Cedric |
author_sort | Albrengues, Jean |
collection | PubMed |
description | Carcinoma-associated fibroblasts (CAF) mediate the onset of a proinvasive tumour microenvironment. The proinflammatory cytokine LIF reprograms fibroblasts into a proinvasive phenotype, which promotes extracellular matrix remodelling and collective invasion of cancer cells. Here we unveil that exposure to LIF initiates an epigenetic switch leading to the constitutive activation of JAK1/STAT3 signalling, which results in sustained proinvasive activity of CAF. Mechanistically, p300-histone acetyltransferase acetylates STAT3, which, in turn, upregulates and activates the DNMT3b DNA methyltransferase. DNMT3b methylates CpG sites of the SHP-1 phosphatase promoter, which abrogates SHP-1 expression, and results in constitutive phosphorylation of JAK1. Sustained JAK1/STAT3 signalling is maintained by DNA methyltransferase DNMT1. Consistently, in human lung and head and neck carcinomas, STAT3 acetylation and phosphorylation are inversely correlated with SHP-1 expression. Combined inhibition of DNMT activities and JAK signalling, in vitro and in vivo, results in long-term reversion of CAF-associated proinvasive activity and restoration of the wild-type fibroblast phenotype. |
format | Online Article Text |
id | pubmed-4682161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46821612015-12-29 Epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts Albrengues, Jean Bertero, Thomas Grasset, Eloise Bonan, Stephanie Maiel, Majdi Bourget, Isabelle Philippe, Claude Herraiz Serrano, Cecilia Benamar, Samia Croce, Olivier Sanz-Moreno, Victoria Meneguzzi, Guerrino Feral, Chloe C. Cristofari, Gael Gaggioli, Cedric Nat Commun Article Carcinoma-associated fibroblasts (CAF) mediate the onset of a proinvasive tumour microenvironment. The proinflammatory cytokine LIF reprograms fibroblasts into a proinvasive phenotype, which promotes extracellular matrix remodelling and collective invasion of cancer cells. Here we unveil that exposure to LIF initiates an epigenetic switch leading to the constitutive activation of JAK1/STAT3 signalling, which results in sustained proinvasive activity of CAF. Mechanistically, p300-histone acetyltransferase acetylates STAT3, which, in turn, upregulates and activates the DNMT3b DNA methyltransferase. DNMT3b methylates CpG sites of the SHP-1 phosphatase promoter, which abrogates SHP-1 expression, and results in constitutive phosphorylation of JAK1. Sustained JAK1/STAT3 signalling is maintained by DNA methyltransferase DNMT1. Consistently, in human lung and head and neck carcinomas, STAT3 acetylation and phosphorylation are inversely correlated with SHP-1 expression. Combined inhibition of DNMT activities and JAK signalling, in vitro and in vivo, results in long-term reversion of CAF-associated proinvasive activity and restoration of the wild-type fibroblast phenotype. Nature Publishing Group 2015-12-15 /pmc/articles/PMC4682161/ /pubmed/26667266 http://dx.doi.org/10.1038/ncomms10204 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Albrengues, Jean Bertero, Thomas Grasset, Eloise Bonan, Stephanie Maiel, Majdi Bourget, Isabelle Philippe, Claude Herraiz Serrano, Cecilia Benamar, Samia Croce, Olivier Sanz-Moreno, Victoria Meneguzzi, Guerrino Feral, Chloe C. Cristofari, Gael Gaggioli, Cedric Epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts |
title | Epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts |
title_full | Epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts |
title_fullStr | Epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts |
title_full_unstemmed | Epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts |
title_short | Epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts |
title_sort | epigenetic switch drives the conversion of fibroblasts into proinvasive cancer-associated fibroblasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682161/ https://www.ncbi.nlm.nih.gov/pubmed/26667266 http://dx.doi.org/10.1038/ncomms10204 |
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