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High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6
The impact of metabolic stress induced by obesity on the bone marrow melanoma niche is largely unknown. Here we employed diet induced obese mice model, where mice received high-fat (HFD) or normal diet (ND) for 6 weeks before challenge with B16F10 melanoma cells. Tumor size, bone loss and osteoclast...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042005/ https://www.ncbi.nlm.nih.gov/pubmed/27049717 http://dx.doi.org/10.18632/oncotarget.8474 |
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author | Chen, Guang-Liang Luo, Yubin Eriksson, Daniel Meng, Xianyi Qian, Cheng Bäuerle, Tobias Chen, Xiao-Xiang Schett, Georg Bozec, Aline |
author_facet | Chen, Guang-Liang Luo, Yubin Eriksson, Daniel Meng, Xianyi Qian, Cheng Bäuerle, Tobias Chen, Xiao-Xiang Schett, Georg Bozec, Aline |
author_sort | Chen, Guang-Liang |
collection | PubMed |
description | The impact of metabolic stress induced by obesity on the bone marrow melanoma niche is largely unknown. Here we employed diet induced obese mice model, where mice received high-fat (HFD) or normal diet (ND) for 6 weeks before challenge with B16F10 melanoma cells. Tumor size, bone loss and osteoclasts numbers were assessed histologically in the tibial bones. For defining the molecular pathway, osteopontin knock-out mice, interleukin 6 neutralizing antibody or Janus kinase 2 inhibition were carried out in the same model. Mechanistic studies such as adipocyte-melanoma co-cultures for defining adipocyte induced changes of tumor cell proliferation and expression profiles were also performed. As results, HFD enhanced melanoma burden in bone by increasing tumor area and osteoclast numbers. This process was associated with higher numbers of bone marrow adipocytes expressing IL-6 in direct vicinity to tumor cells. Inhibition of IL-6 or of downstream JAK2 blocked HFD-induced tumor progression. Furthermore, the phenotypic changes of melanoma cells triggered macrophage and osteoclast accumulation accompanied by increased osteopontin expression. Osteopontin triggered osteoclastogenesis and also exerted a positive feedback loop to tumor cells, which was abrogated in its absence. Metabolic stress by HFD promotes melanoma growth in the bone marrow by an increase in bone marrow adipocytes and IL-6-JAK2-osteopontin mediated activation of tumor cells and osteoclast differentiation. |
format | Online Article Text |
id | pubmed-5042005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50420052016-10-10 High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 Chen, Guang-Liang Luo, Yubin Eriksson, Daniel Meng, Xianyi Qian, Cheng Bäuerle, Tobias Chen, Xiao-Xiang Schett, Georg Bozec, Aline Oncotarget Research Paper The impact of metabolic stress induced by obesity on the bone marrow melanoma niche is largely unknown. Here we employed diet induced obese mice model, where mice received high-fat (HFD) or normal diet (ND) for 6 weeks before challenge with B16F10 melanoma cells. Tumor size, bone loss and osteoclasts numbers were assessed histologically in the tibial bones. For defining the molecular pathway, osteopontin knock-out mice, interleukin 6 neutralizing antibody or Janus kinase 2 inhibition were carried out in the same model. Mechanistic studies such as adipocyte-melanoma co-cultures for defining adipocyte induced changes of tumor cell proliferation and expression profiles were also performed. As results, HFD enhanced melanoma burden in bone by increasing tumor area and osteoclast numbers. This process was associated with higher numbers of bone marrow adipocytes expressing IL-6 in direct vicinity to tumor cells. Inhibition of IL-6 or of downstream JAK2 blocked HFD-induced tumor progression. Furthermore, the phenotypic changes of melanoma cells triggered macrophage and osteoclast accumulation accompanied by increased osteopontin expression. Osteopontin triggered osteoclastogenesis and also exerted a positive feedback loop to tumor cells, which was abrogated in its absence. Metabolic stress by HFD promotes melanoma growth in the bone marrow by an increase in bone marrow adipocytes and IL-6-JAK2-osteopontin mediated activation of tumor cells and osteoclast differentiation. Impact Journals LLC 2016-03-30 /pmc/articles/PMC5042005/ /pubmed/27049717 http://dx.doi.org/10.18632/oncotarget.8474 Text en Copyright: © 2016 Chen et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Chen, Guang-Liang Luo, Yubin Eriksson, Daniel Meng, Xianyi Qian, Cheng Bäuerle, Tobias Chen, Xiao-Xiang Schett, Georg Bozec, Aline High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 |
title | High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 |
title_full | High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 |
title_fullStr | High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 |
title_full_unstemmed | High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 |
title_short | High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 |
title_sort | high fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042005/ https://www.ncbi.nlm.nih.gov/pubmed/27049717 http://dx.doi.org/10.18632/oncotarget.8474 |
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