Cargando…
Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination
Chronic stress induces signalling from the sympathetic nervous system (SNS) and drives cancer progression, although the pathways of tumour cell dissemination are unclear. Here we show that chronic stress restructures lymphatic networks within and around tumours to provide pathways for tumour cell es...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773495/ https://www.ncbi.nlm.nih.gov/pubmed/26925549 http://dx.doi.org/10.1038/ncomms10634 |
_version_ | 1782418752560693248 |
---|---|
author | Le, Caroline P. Nowell, Cameron J. Kim-Fuchs, Corina Botteri, Edoardo Hiller, Jonathan G. Ismail, Hilmy Pimentel, Matthew A. Chai, Ming G. Karnezis, Tara Rotmensz, Nicole Renne, Giuseppe Gandini, Sara Pouton, Colin W. Ferrari, Davide Möller, Andreas Stacker, Steven A. Sloan, Erica K. |
author_facet | Le, Caroline P. Nowell, Cameron J. Kim-Fuchs, Corina Botteri, Edoardo Hiller, Jonathan G. Ismail, Hilmy Pimentel, Matthew A. Chai, Ming G. Karnezis, Tara Rotmensz, Nicole Renne, Giuseppe Gandini, Sara Pouton, Colin W. Ferrari, Davide Möller, Andreas Stacker, Steven A. Sloan, Erica K. |
author_sort | Le, Caroline P. |
collection | PubMed |
description | Chronic stress induces signalling from the sympathetic nervous system (SNS) and drives cancer progression, although the pathways of tumour cell dissemination are unclear. Here we show that chronic stress restructures lymphatic networks within and around tumours to provide pathways for tumour cell escape. We show that VEGFC derived from tumour cells is required for stress to induce lymphatic remodelling and that this depends on COX2 inflammatory signalling from macrophages. Pharmacological inhibition of SNS signalling blocks the effect of chronic stress on lymphatic remodelling in vivo and reduces lymphatic metastasis in preclinical cancer models and in patients with breast cancer. These findings reveal unanticipated communication between stress-induced neural signalling and inflammation, which regulates tumour lymphatic architecture and lymphogenous tumour cell dissemination. These findings suggest that limiting the effects of SNS signalling to prevent tumour cell dissemination through lymphatic routes may provide a strategy to improve cancer outcomes. |
format | Online Article Text |
id | pubmed-4773495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47734952016-03-04 Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination Le, Caroline P. Nowell, Cameron J. Kim-Fuchs, Corina Botteri, Edoardo Hiller, Jonathan G. Ismail, Hilmy Pimentel, Matthew A. Chai, Ming G. Karnezis, Tara Rotmensz, Nicole Renne, Giuseppe Gandini, Sara Pouton, Colin W. Ferrari, Davide Möller, Andreas Stacker, Steven A. Sloan, Erica K. Nat Commun Article Chronic stress induces signalling from the sympathetic nervous system (SNS) and drives cancer progression, although the pathways of tumour cell dissemination are unclear. Here we show that chronic stress restructures lymphatic networks within and around tumours to provide pathways for tumour cell escape. We show that VEGFC derived from tumour cells is required for stress to induce lymphatic remodelling and that this depends on COX2 inflammatory signalling from macrophages. Pharmacological inhibition of SNS signalling blocks the effect of chronic stress on lymphatic remodelling in vivo and reduces lymphatic metastasis in preclinical cancer models and in patients with breast cancer. These findings reveal unanticipated communication between stress-induced neural signalling and inflammation, which regulates tumour lymphatic architecture and lymphogenous tumour cell dissemination. These findings suggest that limiting the effects of SNS signalling to prevent tumour cell dissemination through lymphatic routes may provide a strategy to improve cancer outcomes. Nature Publishing Group 2016-03-01 /pmc/articles/PMC4773495/ /pubmed/26925549 http://dx.doi.org/10.1038/ncomms10634 Text en Copyright © 2016, 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 Le, Caroline P. Nowell, Cameron J. Kim-Fuchs, Corina Botteri, Edoardo Hiller, Jonathan G. Ismail, Hilmy Pimentel, Matthew A. Chai, Ming G. Karnezis, Tara Rotmensz, Nicole Renne, Giuseppe Gandini, Sara Pouton, Colin W. Ferrari, Davide Möller, Andreas Stacker, Steven A. Sloan, Erica K. Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination |
title | Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination |
title_full | Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination |
title_fullStr | Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination |
title_full_unstemmed | Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination |
title_short | Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination |
title_sort | chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773495/ https://www.ncbi.nlm.nih.gov/pubmed/26925549 http://dx.doi.org/10.1038/ncomms10634 |
work_keys_str_mv | AT lecarolinep chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT nowellcameronj chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT kimfuchscorina chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT botteriedoardo chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT hillerjonathang chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT ismailhilmy chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT pimentelmatthewa chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT chaimingg chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT karnezistara chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT rotmensznicole chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT rennegiuseppe chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT gandinisara chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT poutoncolinw chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT ferraridavide chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT mollerandreas chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT stackerstevena chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination AT sloanericak chronicstressinmiceremodelslymphvasculaturetopromotetumourcelldissemination |