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Obesity-associated NLRC4 inflammasome activation drives breast cancer progression

Obesity is associated with an increased risk of developing breast cancer and is also associated with worse clinical prognosis. The mechanistic link between obesity and breast cancer progression remains unclear, and there has been no development of specific treatments to improve the outcome of obese...

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Autores principales: Kolb, Ryan, Phan, Liem, Borcherding, Nicholas, Liu, Yinghong, Yuan, Fang, Janowski, Ann M., Xie, Qing, Markan, Kathleen R., Li, Wei, Potthoff, Matthew J., Fuentes-Mattei, Enrique, Ellies, Lesley G., Knudson, C. Michael, Lee, Mong-Hong, Yeung, Sai-Ching J., Cassel, Suzanne L., Sutterwala, Fayyaz S., Zhang, Weizhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059727/
https://www.ncbi.nlm.nih.gov/pubmed/27708283
http://dx.doi.org/10.1038/ncomms13007
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author Kolb, Ryan
Phan, Liem
Borcherding, Nicholas
Liu, Yinghong
Yuan, Fang
Janowski, Ann M.
Xie, Qing
Markan, Kathleen R.
Li, Wei
Potthoff, Matthew J.
Fuentes-Mattei, Enrique
Ellies, Lesley G.
Knudson, C. Michael
Lee, Mong-Hong
Yeung, Sai-Ching J.
Cassel, Suzanne L.
Sutterwala, Fayyaz S.
Zhang, Weizhou
author_facet Kolb, Ryan
Phan, Liem
Borcherding, Nicholas
Liu, Yinghong
Yuan, Fang
Janowski, Ann M.
Xie, Qing
Markan, Kathleen R.
Li, Wei
Potthoff, Matthew J.
Fuentes-Mattei, Enrique
Ellies, Lesley G.
Knudson, C. Michael
Lee, Mong-Hong
Yeung, Sai-Ching J.
Cassel, Suzanne L.
Sutterwala, Fayyaz S.
Zhang, Weizhou
author_sort Kolb, Ryan
collection PubMed
description Obesity is associated with an increased risk of developing breast cancer and is also associated with worse clinical prognosis. The mechanistic link between obesity and breast cancer progression remains unclear, and there has been no development of specific treatments to improve the outcome of obese cancer patients. Here we show that obesity-associated NLRC4 inflammasome activation/ interleukin (IL)-1 signalling promotes breast cancer progression. The tumour microenvironment in the context of obesity induces an increase in tumour-infiltrating myeloid cells with an activated NLRC4 inflammasome that in turn activates IL-1β, which drives disease progression through adipocyte-mediated vascular endothelial growth factor A (VEGFA) expression and angiogenesis. Further studies show that treatment of mice with metformin inhibits obesity-associated tumour progression associated with a marked decrease in angiogenesis. This report provides a causal mechanism by which obesity promotes breast cancer progression and lays out a foundation to block NLRC4 inflammasome activation or IL-1β signalling transduction that may be useful for the treatment of obese cancer patients.
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spelling pubmed-50597272016-10-26 Obesity-associated NLRC4 inflammasome activation drives breast cancer progression Kolb, Ryan Phan, Liem Borcherding, Nicholas Liu, Yinghong Yuan, Fang Janowski, Ann M. Xie, Qing Markan, Kathleen R. Li, Wei Potthoff, Matthew J. Fuentes-Mattei, Enrique Ellies, Lesley G. Knudson, C. Michael Lee, Mong-Hong Yeung, Sai-Ching J. Cassel, Suzanne L. Sutterwala, Fayyaz S. Zhang, Weizhou Nat Commun Article Obesity is associated with an increased risk of developing breast cancer and is also associated with worse clinical prognosis. The mechanistic link between obesity and breast cancer progression remains unclear, and there has been no development of specific treatments to improve the outcome of obese cancer patients. Here we show that obesity-associated NLRC4 inflammasome activation/ interleukin (IL)-1 signalling promotes breast cancer progression. The tumour microenvironment in the context of obesity induces an increase in tumour-infiltrating myeloid cells with an activated NLRC4 inflammasome that in turn activates IL-1β, which drives disease progression through adipocyte-mediated vascular endothelial growth factor A (VEGFA) expression and angiogenesis. Further studies show that treatment of mice with metformin inhibits obesity-associated tumour progression associated with a marked decrease in angiogenesis. This report provides a causal mechanism by which obesity promotes breast cancer progression and lays out a foundation to block NLRC4 inflammasome activation or IL-1β signalling transduction that may be useful for the treatment of obese cancer patients. Nature Publishing Group 2016-10-06 /pmc/articles/PMC5059727/ /pubmed/27708283 http://dx.doi.org/10.1038/ncomms13007 Text en Copyright © 2016, The Author(s) 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
Kolb, Ryan
Phan, Liem
Borcherding, Nicholas
Liu, Yinghong
Yuan, Fang
Janowski, Ann M.
Xie, Qing
Markan, Kathleen R.
Li, Wei
Potthoff, Matthew J.
Fuentes-Mattei, Enrique
Ellies, Lesley G.
Knudson, C. Michael
Lee, Mong-Hong
Yeung, Sai-Ching J.
Cassel, Suzanne L.
Sutterwala, Fayyaz S.
Zhang, Weizhou
Obesity-associated NLRC4 inflammasome activation drives breast cancer progression
title Obesity-associated NLRC4 inflammasome activation drives breast cancer progression
title_full Obesity-associated NLRC4 inflammasome activation drives breast cancer progression
title_fullStr Obesity-associated NLRC4 inflammasome activation drives breast cancer progression
title_full_unstemmed Obesity-associated NLRC4 inflammasome activation drives breast cancer progression
title_short Obesity-associated NLRC4 inflammasome activation drives breast cancer progression
title_sort obesity-associated nlrc4 inflammasome activation drives breast cancer progression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059727/
https://www.ncbi.nlm.nih.gov/pubmed/27708283
http://dx.doi.org/10.1038/ncomms13007
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