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...
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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. |
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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.</description><identifier>ISSN: 1949-2553</identifier><identifier>EISSN: 1949-2553</identifier><identifier>DOI: 10.18632/oncotarget.8474</identifier><identifier>PMID: 27049717</identifier><language>eng</language><publisher>United States: Impact Journals LLC</publisher><subject>Adipocytes - pathology ; Animals ; Bone Marrow - metabolism ; Bone Marrow - pathology ; Bone Neoplasms - metabolism ; Bone Neoplasms - secondary ; Diet, High-Fat - adverse effects ; Interleukin-6 - metabolism ; Male ; Melanoma, Experimental - metabolism ; Melanoma, Experimental - secondary ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Osteoclasts - pathology ; Osteopontin - metabolism ; Research Paper</subject><ispartof>Oncotarget, 2016-05, Vol.7 (18), p.26653-26669</ispartof><rights>Copyright: © 2016 Chen et al. 2016</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-dca48d9c54413288e15ef182f29f66340f3c7cab1222dd421afc893eb2ad4ef33</citedby><cites>FETCH-LOGICAL-c420t-dca48d9c54413288e15ef182f29f66340f3c7cab1222dd421afc893eb2ad4ef33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042005/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042005/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27049717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Guang-Liang</creatorcontrib><creatorcontrib>Luo, Yubin</creatorcontrib><creatorcontrib>Eriksson, Daniel</creatorcontrib><creatorcontrib>Meng, Xianyi</creatorcontrib><creatorcontrib>Qian, Cheng</creatorcontrib><creatorcontrib>Bäuerle, Tobias</creatorcontrib><creatorcontrib>Chen, Xiao-Xiang</creatorcontrib><creatorcontrib>Schett, Georg</creatorcontrib><creatorcontrib>Bozec, Aline</creatorcontrib><title>High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6</title><title>Oncotarget</title><addtitle>Oncotarget</addtitle><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.</description><subject>Adipocytes - pathology</subject><subject>Animals</subject><subject>Bone Marrow - metabolism</subject><subject>Bone Marrow - pathology</subject><subject>Bone Neoplasms - metabolism</subject><subject>Bone Neoplasms - secondary</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Interleukin-6 - metabolism</subject><subject>Male</subject><subject>Melanoma, Experimental - metabolism</subject><subject>Melanoma, Experimental - secondary</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Osteoclasts - pathology</subject><subject>Osteopontin - metabolism</subject><subject>Research Paper</subject><issn>1949-2553</issn><issn>1949-2553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1vGyEURFWqJkp97ynimIsdvtbLXipFUb4kS7m0Z8TCY02zCy6wrfzvS-o0dbg8eDNvGL1B6AslKyrXnF3FYGLRaYCykqIVH9AZ7US3ZE3DT47up2iR8w9STyNaybpP6JS1RHQtbc-Qf_DDFjtdsPVQsA8mgc6Q8QSjDnHS2MA44iHF32VbYVy2gPsYAE861Sbu97VrZ-PDgGMuEHcxlMrTwVagQBphfq7v9Wf00ekxw-K1nqPvd7ffbh6Wm6f7x5vrzdIIRsrSGi2k7UwjBOVMSqANOCqZY51br7kgjpvW6J4yxqwVjGpnZMehZ9oKcJyfo68H3d3cT2ANhJL0qHbJV8d7FbVX75Hgt2qIv1RDqgHSVIHLV4EUf86Qi5p8ftmCDhDnrKikTLZSSFqp5EA1KeacwL19Q4n6G5L6H5J6CamOXBzbexv4Fwn_A806kvU</recordid><startdate>20160503</startdate><enddate>20160503</enddate><creator>Chen, Guang-Liang</creator><creator>Luo, Yubin</creator><creator>Eriksson, Daniel</creator><creator>Meng, Xianyi</creator><creator>Qian, Cheng</creator><creator>Bäuerle, Tobias</creator><creator>Chen, Xiao-Xiang</creator><creator>Schett, Georg</creator><creator>Bozec, Aline</creator><general>Impact Journals LLC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160503</creationdate><title>High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6</title><author>Chen, Guang-Liang ; Luo, Yubin ; Eriksson, Daniel ; Meng, Xianyi ; Qian, Cheng ; Bäuerle, Tobias ; Chen, Xiao-Xiang ; Schett, Georg ; Bozec, Aline</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-dca48d9c54413288e15ef182f29f66340f3c7cab1222dd421afc893eb2ad4ef33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adipocytes - pathology</topic><topic>Animals</topic><topic>Bone Marrow - metabolism</topic><topic>Bone Marrow - pathology</topic><topic>Bone Neoplasms - metabolism</topic><topic>Bone Neoplasms - secondary</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Interleukin-6 - metabolism</topic><topic>Male</topic><topic>Melanoma, Experimental - metabolism</topic><topic>Melanoma, Experimental - secondary</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Osteoclasts - pathology</topic><topic>Osteopontin - metabolism</topic><topic>Research Paper</topic><toplevel>online_resources</toplevel><creatorcontrib>Chen, Guang-Liang</creatorcontrib><creatorcontrib>Luo, Yubin</creatorcontrib><creatorcontrib>Eriksson, Daniel</creatorcontrib><creatorcontrib>Meng, Xianyi</creatorcontrib><creatorcontrib>Qian, Cheng</creatorcontrib><creatorcontrib>Bäuerle, Tobias</creatorcontrib><creatorcontrib>Chen, Xiao-Xiang</creatorcontrib><creatorcontrib>Schett, Georg</creatorcontrib><creatorcontrib>Bozec, Aline</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncotarget</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Guang-Liang</au><au>Luo, Yubin</au><au>Eriksson, Daniel</au><au>Meng, Xianyi</au><au>Qian, Cheng</au><au>Bäuerle, Tobias</au><au>Chen, Xiao-Xiang</au><au>Schett, Georg</au><au>Bozec, Aline</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6</atitle><jtitle>Oncotarget</jtitle><addtitle>Oncotarget</addtitle><date>2016-05-03</date><risdate>2016</risdate><volume>7</volume><issue>18</issue><spage>26653</spage><epage>26669</epage><pages>26653-26669</pages><issn>1949-2553</issn><eissn>1949-2553</eissn><abstract>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.</abstract><cop>United States</cop><pub>Impact Journals LLC</pub><pmid>27049717</pmid><doi>10.18632/oncotarget.8474</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adipocytes - pathology Animals Bone Marrow - metabolism Bone Marrow - pathology Bone Neoplasms - metabolism Bone Neoplasms - secondary Diet, High-Fat - adverse effects Interleukin-6 - metabolism Male Melanoma, Experimental - metabolism Melanoma, Experimental - secondary Mice Mice, Inbred C57BL Mice, Knockout Osteoclasts - pathology Osteopontin - metabolism Research Paper |
title | High fat diet increases melanoma cell growth in the bone marrow by inducing osteopontin and interleukin 6 |
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