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A ZEB1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours
Accumulating evidence indicates that the zinc-finger transcription factor ZEB1 is predominantly expressed in the stroma of several tumours. However, the role of stromal ZEB1 in tumour progression remains unexplored. In this study, while interrogating human databases, we uncover a remarkable decrease...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642263/ https://www.ncbi.nlm.nih.gov/pubmed/31324807 http://dx.doi.org/10.1038/s41467-019-11278-7 |
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author | Fu, Rong Han, Chen-Feng Ni, Ting Di, Lei Liu, Li-Juan Lv, Wen-Cong Bi, Yan-Ran Jiang, Nan He, Yin Li, Hong-Mei Wang, Shui Xie, Hui Chen, Bao-An Wang, Xiao-Sheng Weiss, Stephen J. Lu, Tao Guo, Qing-Long Wu, Zhao-Qiu |
author_facet | Fu, Rong Han, Chen-Feng Ni, Ting Di, Lei Liu, Li-Juan Lv, Wen-Cong Bi, Yan-Ran Jiang, Nan He, Yin Li, Hong-Mei Wang, Shui Xie, Hui Chen, Bao-An Wang, Xiao-Sheng Weiss, Stephen J. Lu, Tao Guo, Qing-Long Wu, Zhao-Qiu |
author_sort | Fu, Rong |
collection | PubMed |
description | Accumulating evidence indicates that the zinc-finger transcription factor ZEB1 is predominantly expressed in the stroma of several tumours. However, the role of stromal ZEB1 in tumour progression remains unexplored. In this study, while interrogating human databases, we uncover a remarkable decrease in relapse-free survival of breast cancer patients expressing high ZEB1 levels in the stroma. Using a mouse model of breast cancer, we show that ZEB1 inactivation in stromal fibroblasts suppresses tumour initiation, progression and metastasis. We associate this with reduced extracellular matrix remodeling, immune cell infiltration and decreased angiogenesis. ZEB1 deletion in stromal fibroblasts increases acetylation, expression and recruitment of p53 to FGF2/7, VEGF and IL6 promoters, thereby reducing their production and secretion into the surrounding stroma. Importantly, p53 ablation in ZEB1 stroma-deleted mammary tumours sufficiently recovers the impaired cancer growth and progression. Our findings identify the ZEB1/p53 axis as a stroma-specific signaling pathway that promotes mammary epithelial tumours. |
format | Online Article Text |
id | pubmed-6642263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66422632019-07-22 A ZEB1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours Fu, Rong Han, Chen-Feng Ni, Ting Di, Lei Liu, Li-Juan Lv, Wen-Cong Bi, Yan-Ran Jiang, Nan He, Yin Li, Hong-Mei Wang, Shui Xie, Hui Chen, Bao-An Wang, Xiao-Sheng Weiss, Stephen J. Lu, Tao Guo, Qing-Long Wu, Zhao-Qiu Nat Commun Article Accumulating evidence indicates that the zinc-finger transcription factor ZEB1 is predominantly expressed in the stroma of several tumours. However, the role of stromal ZEB1 in tumour progression remains unexplored. In this study, while interrogating human databases, we uncover a remarkable decrease in relapse-free survival of breast cancer patients expressing high ZEB1 levels in the stroma. Using a mouse model of breast cancer, we show that ZEB1 inactivation in stromal fibroblasts suppresses tumour initiation, progression and metastasis. We associate this with reduced extracellular matrix remodeling, immune cell infiltration and decreased angiogenesis. ZEB1 deletion in stromal fibroblasts increases acetylation, expression and recruitment of p53 to FGF2/7, VEGF and IL6 promoters, thereby reducing their production and secretion into the surrounding stroma. Importantly, p53 ablation in ZEB1 stroma-deleted mammary tumours sufficiently recovers the impaired cancer growth and progression. Our findings identify the ZEB1/p53 axis as a stroma-specific signaling pathway that promotes mammary epithelial tumours. Nature Publishing Group UK 2019-07-19 /pmc/articles/PMC6642263/ /pubmed/31324807 http://dx.doi.org/10.1038/s41467-019-11278-7 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Fu, Rong Han, Chen-Feng Ni, Ting Di, Lei Liu, Li-Juan Lv, Wen-Cong Bi, Yan-Ran Jiang, Nan He, Yin Li, Hong-Mei Wang, Shui Xie, Hui Chen, Bao-An Wang, Xiao-Sheng Weiss, Stephen J. Lu, Tao Guo, Qing-Long Wu, Zhao-Qiu A ZEB1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours |
title | A ZEB1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours |
title_full | A ZEB1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours |
title_fullStr | A ZEB1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours |
title_full_unstemmed | A ZEB1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours |
title_short | A ZEB1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours |
title_sort | zeb1/p53 signaling axis in stromal fibroblasts promotes mammary epithelial tumours |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642263/ https://www.ncbi.nlm.nih.gov/pubmed/31324807 http://dx.doi.org/10.1038/s41467-019-11278-7 |
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