Lumican and decorin are differentially expressed in human breast carcinoma

Previous studies have shown that lumican is expressed and increased in the stroma of breast tumours. Lumican expression has now been examined relative to other members of the small leucine‐rich proteoglycan gene family in normal and neoplastic breast tissues, to begin to determine its role in breast...

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Veröffentlicht in:The Journal of pathology 2000-11, Vol.192 (3), p.313-320
Hauptverfasser: Leygue, Etienne, Snell, Linda, Dotzlaw, Helmut, Troup, Sandra, Hiller-Hitchcock, Tamara, Murphy, Leigh C., Roughley, Peter J., Watson, Peter H.
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container_end_page 320
container_issue 3
container_start_page 313
container_title The Journal of pathology
container_volume 192
creator Leygue, Etienne
Snell, Linda
Dotzlaw, Helmut
Troup, Sandra
Hiller-Hitchcock, Tamara
Murphy, Leigh C.
Roughley, Peter J.
Watson, Peter H.
description Previous studies have shown that lumican is expressed and increased in the stroma of breast tumours. Lumican expression has now been examined relative to other members of the small leucine‐rich proteoglycan gene family in normal and neoplastic breast tissues, to begin to determine its role in breast tumour progression. Western blot study showed that lumican protein is highly abundant relative to decorin, while biglycan and fibromodulin are only detected occasionally in breast tissues (n=15 cases). Further analysis of lumican and decorin expression performed in matched normal and tumour tissues by in situ hybridization showed that both mRNAs were expressed by similar fibroblast‐like cells adjacent to epithelium. However, lumican mRNA expression was significantly increased in tumours (n=34, p
doi_str_mv 10.1002/1096-9896(200011)192:3<313::AID-PATH694>3.0.CO;2-B
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Lumican expression has now been examined relative to other members of the small leucine‐rich proteoglycan gene family in normal and neoplastic breast tissues, to begin to determine its role in breast tumour progression. Western blot study showed that lumican protein is highly abundant relative to decorin, while biglycan and fibromodulin are only detected occasionally in breast tissues (n=15 cases). Further analysis of lumican and decorin expression performed in matched normal and tumour tissues by in situ hybridization showed that both mRNAs were expressed by similar fibroblast‐like cells adjacent to epithelium. However, lumican mRNA expression was significantly increased in tumours (n=34, p&lt;0.0001), while decorin mRNA was decreased (p=0.0002) in neoplastic relative to adjacent normal stroma. This was accompanied by a significant increase in lumican protein (n=12, p=0.0122), but not decorin. Further evidence of altered lumican expression in breast cancer was manifested by discordance between lumican mRNA and protein localization in some regions of tumours but not in adjacent morphologically normal tissues. It is concluded that lumican is the most abundant of these proteoglycans in breast tumours and that lumican and decorin are inversely regulated in association with breast tumourigenesis. 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Pathol</addtitle><description>Previous studies have shown that lumican is expressed and increased in the stroma of breast tumours. Lumican expression has now been examined relative to other members of the small leucine‐rich proteoglycan gene family in normal and neoplastic breast tissues, to begin to determine its role in breast tumour progression. Western blot study showed that lumican protein is highly abundant relative to decorin, while biglycan and fibromodulin are only detected occasionally in breast tissues (n=15 cases). Further analysis of lumican and decorin expression performed in matched normal and tumour tissues by in situ hybridization showed that both mRNAs were expressed by similar fibroblast‐like cells adjacent to epithelium. However, lumican mRNA expression was significantly increased in tumours (n=34, p&lt;0.0001), while decorin mRNA was decreased (p=0.0002) in neoplastic relative to adjacent normal stroma. This was accompanied by a significant increase in lumican protein (n=12, p=0.0122), but not decorin. Further evidence of altered lumican expression in breast cancer was manifested by discordance between lumican mRNA and protein localization in some regions of tumours but not in adjacent morphologically normal tissues. It is concluded that lumican is the most abundant of these proteoglycans in breast tumours and that lumican and decorin are inversely regulated in association with breast tumourigenesis. 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Obstetrics</subject><subject>Humans</subject><subject>In Situ Hybridization</subject><subject>lumican</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Proteoglycans - genetics</subject><subject>Proteoglycans - metabolism</subject><subject>RNA, Messenger - analysis</subject><subject>small leucine-rich proteoglycan</subject><subject>Tumors</subject><subject>tumour progression</subject><issn>0022-3417</issn><issn>1096-9896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkF2LEzEUQIMobnf1L8iAIO7D1GSSmTRVhG7V_aBrl6Xo4yWT3MHofNSkg9t_b8qM9cUXnxKSk5PLIWTO6JRRmr1hVBWpmqnidUYpZeycqWzO33HG5_PF9Yf0brG5KpR4z6d0uly_zdKLR2RyfPSYTKIkS7lg8oSchvA9SpTK86fkhDGaC8nEhNys-sYZ3Sa6tYlF03kX9x4T66oKPbY7p-t6n-DD1mMIaJN4_61v4ovSow67xGhvXNs1-hl5Uuk64PNxPSObTx83y6t0tb68Xi5WqRGKi3Qm8kJnqK1EUVRCW0uVtRVWhhtjpOY0rwprJDKlRIkzw3mZU8tzKgWqkp-RV4N267ufPYYdNC4YrGvdYtcHkBmXShSzCN4PoPFdCB4r2HrXaL8HRuEQGA6t4NAKhsAQAwOHGBggBoYxcDyisFxDBhdR-mL8vS8btH-VY9EIvBwBHYyuK69b48KRkypTPIvUl4H65Wrc_89g_57rz1EUp4PYhR0-HMXa_4BCcpnD18-XcHvP7_jq9gYE_w0WM7Eg</recordid><startdate>200011</startdate><enddate>200011</enddate><creator>Leygue, Etienne</creator><creator>Snell, Linda</creator><creator>Dotzlaw, Helmut</creator><creator>Troup, Sandra</creator><creator>Hiller-Hitchcock, Tamara</creator><creator>Murphy, Leigh C.</creator><creator>Roughley, Peter J.</creator><creator>Watson, Peter H.</creator><general>John Wiley &amp; Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><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></search><sort><creationdate>200011</creationdate><title>Lumican and decorin are differentially expressed in human breast carcinoma</title><author>Leygue, Etienne ; Snell, Linda ; Dotzlaw, Helmut ; Troup, Sandra ; Hiller-Hitchcock, Tamara ; Murphy, Leigh C. ; Roughley, Peter J. ; Watson, Peter H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4934-8456a2ead7e46f4add09ddfefc3ccc7a305f6dc7e1994be8c33b50d35074e9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor</topic><topic>Blotting, Western</topic><topic>breast cancer</topic><topic>Breast Neoplasms - metabolism</topic><topic>Case-Control Studies</topic><topic>decorin</topic><topic>Disease Progression</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>In Situ Hybridization</topic><topic>lumican</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Proteoglycans - genetics</topic><topic>Proteoglycans - metabolism</topic><topic>RNA, Messenger - analysis</topic><topic>small leucine-rich proteoglycan</topic><topic>Tumors</topic><topic>tumour progression</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leygue, Etienne</creatorcontrib><creatorcontrib>Snell, Linda</creatorcontrib><creatorcontrib>Dotzlaw, Helmut</creatorcontrib><creatorcontrib>Troup, Sandra</creatorcontrib><creatorcontrib>Hiller-Hitchcock, Tamara</creatorcontrib><creatorcontrib>Murphy, Leigh C.</creatorcontrib><creatorcontrib>Roughley, Peter J.</creatorcontrib><creatorcontrib>Watson, Peter H.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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><jtitle>The Journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leygue, Etienne</au><au>Snell, Linda</au><au>Dotzlaw, Helmut</au><au>Troup, Sandra</au><au>Hiller-Hitchcock, Tamara</au><au>Murphy, Leigh C.</au><au>Roughley, Peter J.</au><au>Watson, Peter H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lumican and decorin are differentially expressed in human breast carcinoma</atitle><jtitle>The Journal of pathology</jtitle><addtitle>J. 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subjects Adult
Aged
Biological and medical sciences
Biomarkers, Tumor
Blotting, Western
breast cancer
Breast Neoplasms - metabolism
Case-Control Studies
decorin
Disease Progression
Electrophoresis, Polyacrylamide Gel
Female
Gene Expression
Gynecology. Andrology. Obstetrics
Humans
In Situ Hybridization
lumican
Mammary gland diseases
Medical sciences
Middle Aged
Proteoglycans - genetics
Proteoglycans - metabolism
RNA, Messenger - analysis
small leucine-rich proteoglycan
Tumors
tumour progression
title Lumican and decorin are differentially expressed in human breast carcinoma
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