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Osteopontin promotes aromatase expression and estradiol production in human adipocytes
Breast and endometrial cancer are often estrogen dependent, and their incidence and mortality are increased by obesity in postmenopausal women. Osteopontin (OPN) is a cytokine strongly upregulated in adipose tissue (AT) in obesity. OPN function is potentiated by cleavage by matrix metalloproteinases...
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Published in: | Breast cancer research and treatment 2015-11, Vol.154 (1), p.63-69 |
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container_title | Breast cancer research and treatment |
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description | Breast and endometrial cancer are often estrogen dependent, and their incidence and mortality are increased by obesity in postmenopausal women. Osteopontin (OPN) is a cytokine strongly upregulated in adipose tissue (AT) in obesity. OPN function is potentiated by cleavage by matrix metalloproteinases (MMP). OPN and MMPs play a role in cancer development and are prognostic markers in breast cancer progression. While induction of the estrogen-synthesizing enzyme aromatase by TNFa and IL1 has been shown in preadipocytes, an impact of OPN on aromatase expression in AT has not been investigated yet. Gene expression was determined in AT samples of 21 morbidly obese and matched non-obese subjects. Primary human adipocytes were treated with full-length OPN or MMP-cleaved OPN (cOPN). Protein and mRNA expressions were analyzed from cell lysates, or cells were subsequently supplied with testosterone to determine estradiol production and for indirect co-culture with the estrogen-dependent MCF-7 cell line. Aromatase expression strongly correlated with gene expression of OPN and various MMPs in visceral and MMPs in subcutaneous AT, but not with TNFα expression in both tissues. In vitro, cOPN more effectively than full-length OPN upregulated aromatase mRNA in adipocytes and significantly increased aromatase protein level and estradiol production, leading to increased MCF-7 growth in indirect co-culture. OPN and MMPs are upregulated in AT in obesity, and MMP-cleaved OPN is particularly effective in inducing aromatase activity in human adipocytes. Thereby, obesity-induced OPN expression in AT may contribute to estradiol production and thus to the association of obesity with estrogen-dependent cancers. |
doi_str_mv | 10.1007/s10549-015-3603-0 |
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Osteopontin (OPN) is a cytokine strongly upregulated in adipose tissue (AT) in obesity. OPN function is potentiated by cleavage by matrix metalloproteinases (MMP). OPN and MMPs play a role in cancer development and are prognostic markers in breast cancer progression. While induction of the estrogen-synthesizing enzyme aromatase by TNFa and IL1 has been shown in preadipocytes, an impact of OPN on aromatase expression in AT has not been investigated yet. Gene expression was determined in AT samples of 21 morbidly obese and matched non-obese subjects. Primary human adipocytes were treated with full-length OPN or MMP-cleaved OPN (cOPN). Protein and mRNA expressions were analyzed from cell lysates, or cells were subsequently supplied with testosterone to determine estradiol production and for indirect co-culture with the estrogen-dependent MCF-7 cell line. Aromatase expression strongly correlated with gene expression of OPN and various MMPs in visceral and MMPs in subcutaneous AT, but not with TNFα expression in both tissues. In vitro, cOPN more effectively than full-length OPN upregulated aromatase mRNA in adipocytes and significantly increased aromatase protein level and estradiol production, leading to increased MCF-7 growth in indirect co-culture. OPN and MMPs are upregulated in AT in obesity, and MMP-cleaved OPN is particularly effective in inducing aromatase activity in human adipocytes. Thereby, obesity-induced OPN expression in AT may contribute to estradiol production and thus to the association of obesity with estrogen-dependent cancers.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-015-3603-0</identifier><identifier>PMID: 26482249</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adipocytes - drug effects ; Adipocytes - metabolism ; Adipogenesis - genetics ; Adipose Tissue - metabolism ; Adipose tissues ; Analysis ; Aromatase - genetics ; Aromatase - metabolism ; Breast cancer ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Cancer research ; Cancer therapies ; Cell Proliferation ; Cells, Cultured ; Cytokines ; Endometrial cancer ; Enzymes ; Estradiol ; Estradiol - biosynthesis ; Female ; Gene Expression ; Gene Expression Regulation - drug effects ; Health aspects ; Humans ; Matrix ; Matrix Metalloproteinases - genetics ; Matrix Metalloproteinases - metabolism ; MCF-7 Cells ; Medicine ; Medicine & Public Health ; Mortality ; Obesity ; Obesity - genetics ; Obesity - metabolism ; Oncology ; Osteopontin - genetics ; Osteopontin - metabolism ; Osteopontin - pharmacology ; Phenols ; Postmenopausal women ; Preclinical Study ; RNA ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Testosterone</subject><ispartof>Breast cancer research and treatment, 2015-11, Vol.154 (1), p.63-69</ispartof><rights>Springer Science+Business Media New York 2015</rights><rights>COPYRIGHT 2015 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-9442284cdb7bfcafee06a7377df177d801dacffcdad9a2c56ced56af382cb3943</citedby><cites>FETCH-LOGICAL-c470t-9442284cdb7bfcafee06a7377df177d801dacffcdad9a2c56ced56af382cb3943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26482249$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leitner, Lukas</creatorcontrib><creatorcontrib>Jürets, Alexander</creatorcontrib><creatorcontrib>Itariu, Bianca K.</creatorcontrib><creatorcontrib>Keck, Maike</creatorcontrib><creatorcontrib>Prager, Gerhard</creatorcontrib><creatorcontrib>Langer, Felix</creatorcontrib><creatorcontrib>Grablowitz, Viktor</creatorcontrib><creatorcontrib>Zeyda, Maximilian</creatorcontrib><creatorcontrib>Stulnig, Thomas M.</creatorcontrib><title>Osteopontin promotes aromatase expression and estradiol production in human adipocytes</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Breast and endometrial cancer are often estrogen dependent, and their incidence and mortality are increased by obesity in postmenopausal women. Osteopontin (OPN) is a cytokine strongly upregulated in adipose tissue (AT) in obesity. OPN function is potentiated by cleavage by matrix metalloproteinases (MMP). OPN and MMPs play a role in cancer development and are prognostic markers in breast cancer progression. While induction of the estrogen-synthesizing enzyme aromatase by TNFa and IL1 has been shown in preadipocytes, an impact of OPN on aromatase expression in AT has not been investigated yet. Gene expression was determined in AT samples of 21 morbidly obese and matched non-obese subjects. Primary human adipocytes were treated with full-length OPN or MMP-cleaved OPN (cOPN). Protein and mRNA expressions were analyzed from cell lysates, or cells were subsequently supplied with testosterone to determine estradiol production and for indirect co-culture with the estrogen-dependent MCF-7 cell line. Aromatase expression strongly correlated with gene expression of OPN and various MMPs in visceral and MMPs in subcutaneous AT, but not with TNFα expression in both tissues. In vitro, cOPN more effectively than full-length OPN upregulated aromatase mRNA in adipocytes and significantly increased aromatase protein level and estradiol production, leading to increased MCF-7 growth in indirect co-culture. OPN and MMPs are upregulated in AT in obesity, and MMP-cleaved OPN is particularly effective in inducing aromatase activity in human adipocytes. Thereby, obesity-induced OPN expression in AT may contribute to estradiol production and thus to the association of obesity with estrogen-dependent cancers.</description><subject>Adipocytes - drug effects</subject><subject>Adipocytes - metabolism</subject><subject>Adipogenesis - genetics</subject><subject>Adipose Tissue - metabolism</subject><subject>Adipose tissues</subject><subject>Analysis</subject><subject>Aromatase - genetics</subject><subject>Aromatase - metabolism</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Cytokines</subject><subject>Endometrial cancer</subject><subject>Enzymes</subject><subject>Estradiol</subject><subject>Estradiol - biosynthesis</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Matrix</subject><subject>Matrix Metalloproteinases - genetics</subject><subject>Matrix Metalloproteinases - metabolism</subject><subject>MCF-7 Cells</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mortality</subject><subject>Obesity</subject><subject>Obesity - genetics</subject><subject>Obesity - metabolism</subject><subject>Oncology</subject><subject>Osteopontin - genetics</subject><subject>Osteopontin - metabolism</subject><subject>Osteopontin - pharmacology</subject><subject>Phenols</subject><subject>Postmenopausal women</subject><subject>Preclinical Study</subject><subject>RNA</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Testosterone</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1kVtrFTEUhYMo9lj9Ab7IgCC-TN25TDJ5LMUbFPqivoacZKdnykwyJjNg_70ZTtVWlEASsr-12DuLkJcUziiAelcodEK3QLuWS-AtPCI72ineKkbVY7IDKlUre5An5FkpNwCgFein5IRJ0TMm9I58uyoLpjnFZYjNnNOUFiyNrRe72IIN_pgzljKk2NjoGyxLtn5I48b61S1boSoP62Qr4Yc5udvq8Jw8CXYs-OLuPCVfP7z_cvGpvbz6-Pni_LJ1QsHSaiEY64Xze7UPzgZEkFZxpXygdeuBeutCcN56bZnrpEPfSRt4z9yea8FPydujb23n-1q7M9NQHI6jjZjWYqiSQmpN-w19_Rd6k9Yca3eVYoqLXmj-h7q2I5ohhlQHdpupORdc9aoHJSt19g-qLo_T4FLEMNT3B4I39wQHtONyKGlct_8rD0F6BF1OpWQMZs7DZPOtoWC20M0xdFNDN1voBqrm1d1k635C_1vxK-UKsCNQaileY743-n9dfwIAdrcM</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Leitner, Lukas</creator><creator>Jürets, Alexander</creator><creator>Itariu, Bianca K.</creator><creator>Keck, Maike</creator><creator>Prager, Gerhard</creator><creator>Langer, Felix</creator><creator>Grablowitz, Viktor</creator><creator>Zeyda, Maximilian</creator><creator>Stulnig, Thomas M.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20151101</creationdate><title>Osteopontin promotes aromatase expression and estradiol production in human adipocytes</title><author>Leitner, Lukas ; Jürets, Alexander ; Itariu, Bianca K. ; Keck, Maike ; Prager, Gerhard ; Langer, Felix ; Grablowitz, Viktor ; Zeyda, Maximilian ; Stulnig, Thomas M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-9442284cdb7bfcafee06a7377df177d801dacffcdad9a2c56ced56af382cb3943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adipocytes - drug effects</topic><topic>Adipocytes - metabolism</topic><topic>Adipogenesis - genetics</topic><topic>Adipose Tissue - metabolism</topic><topic>Adipose tissues</topic><topic>Analysis</topic><topic>Aromatase - genetics</topic><topic>Aromatase - metabolism</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Cancer research</topic><topic>Cancer therapies</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Cytokines</topic><topic>Endometrial cancer</topic><topic>Enzymes</topic><topic>Estradiol</topic><topic>Estradiol - biosynthesis</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Matrix</topic><topic>Matrix Metalloproteinases - genetics</topic><topic>Matrix Metalloproteinases - metabolism</topic><topic>MCF-7 Cells</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mortality</topic><topic>Obesity</topic><topic>Obesity - genetics</topic><topic>Obesity - metabolism</topic><topic>Oncology</topic><topic>Osteopontin - genetics</topic><topic>Osteopontin - metabolism</topic><topic>Osteopontin - pharmacology</topic><topic>Phenols</topic><topic>Postmenopausal women</topic><topic>Preclinical Study</topic><topic>RNA</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Testosterone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leitner, Lukas</creatorcontrib><creatorcontrib>Jürets, Alexander</creatorcontrib><creatorcontrib>Itariu, Bianca K.</creatorcontrib><creatorcontrib>Keck, Maike</creatorcontrib><creatorcontrib>Prager, Gerhard</creatorcontrib><creatorcontrib>Langer, Felix</creatorcontrib><creatorcontrib>Grablowitz, Viktor</creatorcontrib><creatorcontrib>Zeyda, Maximilian</creatorcontrib><creatorcontrib>Stulnig, Thomas M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Databases</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leitner, Lukas</au><au>Jürets, Alexander</au><au>Itariu, Bianca K.</au><au>Keck, Maike</au><au>Prager, Gerhard</au><au>Langer, Felix</au><au>Grablowitz, Viktor</au><au>Zeyda, Maximilian</au><au>Stulnig, Thomas M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteopontin promotes aromatase expression and estradiol production in human adipocytes</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>154</volume><issue>1</issue><spage>63</spage><epage>69</epage><pages>63-69</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>Breast and endometrial cancer are often estrogen dependent, and their incidence and mortality are increased by obesity in postmenopausal women. Osteopontin (OPN) is a cytokine strongly upregulated in adipose tissue (AT) in obesity. OPN function is potentiated by cleavage by matrix metalloproteinases (MMP). OPN and MMPs play a role in cancer development and are prognostic markers in breast cancer progression. While induction of the estrogen-synthesizing enzyme aromatase by TNFa and IL1 has been shown in preadipocytes, an impact of OPN on aromatase expression in AT has not been investigated yet. Gene expression was determined in AT samples of 21 morbidly obese and matched non-obese subjects. Primary human adipocytes were treated with full-length OPN or MMP-cleaved OPN (cOPN). Protein and mRNA expressions were analyzed from cell lysates, or cells were subsequently supplied with testosterone to determine estradiol production and for indirect co-culture with the estrogen-dependent MCF-7 cell line. Aromatase expression strongly correlated with gene expression of OPN and various MMPs in visceral and MMPs in subcutaneous AT, but not with TNFα expression in both tissues. In vitro, cOPN more effectively than full-length OPN upregulated aromatase mRNA in adipocytes and significantly increased aromatase protein level and estradiol production, leading to increased MCF-7 growth in indirect co-culture. OPN and MMPs are upregulated in AT in obesity, and MMP-cleaved OPN is particularly effective in inducing aromatase activity in human adipocytes. Thereby, obesity-induced OPN expression in AT may contribute to estradiol production and thus to the association of obesity with estrogen-dependent cancers.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>26482249</pmid><doi>10.1007/s10549-015-3603-0</doi><tpages>7</tpages></addata></record> |
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subjects | Adipocytes - drug effects Adipocytes - metabolism Adipogenesis - genetics Adipose Tissue - metabolism Adipose tissues Analysis Aromatase - genetics Aromatase - metabolism Breast cancer Breast Neoplasms - genetics Breast Neoplasms - metabolism Cancer research Cancer therapies Cell Proliferation Cells, Cultured Cytokines Endometrial cancer Enzymes Estradiol Estradiol - biosynthesis Female Gene Expression Gene Expression Regulation - drug effects Health aspects Humans Matrix Matrix Metalloproteinases - genetics Matrix Metalloproteinases - metabolism MCF-7 Cells Medicine Medicine & Public Health Mortality Obesity Obesity - genetics Obesity - metabolism Oncology Osteopontin - genetics Osteopontin - metabolism Osteopontin - pharmacology Phenols Postmenopausal women Preclinical Study RNA RNA, Messenger - genetics RNA, Messenger - metabolism Testosterone |
title | Osteopontin promotes aromatase expression and estradiol production in human adipocytes |
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