Use of CD10 as a marker of canine mammary myoepithelial cells
CD10 is an important cell marker in the diagnosis of acute lymphoblastic leukaemia and of breast myoepithelial (ME) cells in humans. The objective of this study was to assess the value of CD10 as a marker of canine ME cells using immunohistochemistry on routinely processed normal, dysplastic and neo...
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Veröffentlicht in: | The veterinary journal (1997) 2013-02, Vol.195 (2), p.192-199 |
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container_title | The veterinary journal (1997) |
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creator | Sánchez-Céspedes, R. Suárez-Bonnet, A. Millán, Y. Guil-Luna, S. Reymundo, C. Herráez, P. Espinosa de los Monteros, A. Martin de las Mulas, J. |
description | CD10 is an important cell marker in the diagnosis of acute lymphoblastic leukaemia and of breast myoepithelial (ME) cells in humans. The objective of this study was to assess the value of CD10 as a marker of canine ME cells using immunohistochemistry on routinely processed normal, dysplastic and neoplastic mammary tissue. Five different CD10 positive cell types were identified on the basis of cell morphology, pattern of immunoreactivity, and on the co-expression of additional cell lineage-specific markers.
Type 1 cells were typical fusiform cells with a ME cell phenotype (calponin- and cytokeratin [CK] 14-positive, CK8/18-negative). Type 2 cells were typical or atypical polyhedral cells with a luminal epithelial (LE) cell phenotype (calponin- and CK14-negative, CK8/18-positive). Type 3 cells had a type 1 phenotype with variable morphology, and type 4 were atypical neoplastic cells with a mixed ME/LE phenotype. Type 5 cells were typical fusiform cells with a stromal phenotype.
Type 1 cells were considered normal ME cells and were found in all sample types; type 2 cells were considered normal or neoplastic LE cells and were also found in all sample types; types 3 and 4 cells were restricted to tumour samples and to malignant tumours, respectively, and type 5 cells were found in all sample types, although predominantly in neoplastic tissue. The findings indicate that the CD10 antigen is a sensitive (although not specific) marker of canine ME cells in normal, dysplastic and neoplastic mammary tissue. Differences in the distribution and staining intensity of CD10-positive cells suggest a number of potential roles for this protein in the pathogenesis of canine mammary neoplasia. |
doi_str_mv | 10.1016/j.tvjl.2012.06.003 |
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Type 1 cells were typical fusiform cells with a ME cell phenotype (calponin- and cytokeratin [CK] 14-positive, CK8/18-negative). Type 2 cells were typical or atypical polyhedral cells with a luminal epithelial (LE) cell phenotype (calponin- and CK14-negative, CK8/18-positive). Type 3 cells had a type 1 phenotype with variable morphology, and type 4 were atypical neoplastic cells with a mixed ME/LE phenotype. Type 5 cells were typical fusiform cells with a stromal phenotype.
Type 1 cells were considered normal ME cells and were found in all sample types; type 2 cells were considered normal or neoplastic LE cells and were also found in all sample types; types 3 and 4 cells were restricted to tumour samples and to malignant tumours, respectively, and type 5 cells were found in all sample types, although predominantly in neoplastic tissue. The findings indicate that the CD10 antigen is a sensitive (although not specific) marker of canine ME cells in normal, dysplastic and neoplastic mammary tissue. Differences in the distribution and staining intensity of CD10-positive cells suggest a number of potential roles for this protein in the pathogenesis of canine mammary neoplasia.</description><identifier>ISSN: 1090-0233</identifier><identifier>EISSN: 1532-2971</identifier><identifier>DOI: 10.1016/j.tvjl.2012.06.003</identifier><identifier>PMID: 22819182</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adenoma - metabolism ; Adenoma - veterinary ; Animals ; antigens ; Biomarkers, Tumor ; Calcium-Binding Proteins - genetics ; Calcium-Binding Proteins - metabolism ; Calponins ; Canine ; Carcinoma - metabolism ; Carcinoma - veterinary ; CD10 ; Dog Diseases - genetics ; Dog Diseases - metabolism ; Dogs ; Female ; Gene Expression Regulation - physiology ; humans ; immunohistochemistry ; Keratin-14 - genetics ; Keratin-14 - metabolism ; leukemia ; Mammary Neoplasms, Animal - metabolism ; Mammary tumours ; Microfilament Proteins - genetics ; Microfilament Proteins - metabolism ; Myoepithelium ; Neprilysin - genetics ; Neprilysin - metabolism ; pathogenesis ; phenotype ; Staining and Labeling ; stromal cells</subject><ispartof>The veterinary journal (1997), 2013-02, Vol.195 (2), p.192-199</ispartof><rights>2012 Elsevier Ltd</rights><rights>Copyright © 2012 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-a91ffd3a56432802f5c994b02763e3e7956c6e41218d68632a7596c9611a1e143</citedby><cites>FETCH-LOGICAL-c380t-a91ffd3a56432802f5c994b02763e3e7956c6e41218d68632a7596c9611a1e143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tvjl.2012.06.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27913,27914,45984</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22819182$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sánchez-Céspedes, R.</creatorcontrib><creatorcontrib>Suárez-Bonnet, A.</creatorcontrib><creatorcontrib>Millán, Y.</creatorcontrib><creatorcontrib>Guil-Luna, S.</creatorcontrib><creatorcontrib>Reymundo, C.</creatorcontrib><creatorcontrib>Herráez, P.</creatorcontrib><creatorcontrib>Espinosa de los Monteros, A.</creatorcontrib><creatorcontrib>Martin de las Mulas, J.</creatorcontrib><title>Use of CD10 as a marker of canine mammary myoepithelial cells</title><title>The veterinary journal (1997)</title><addtitle>Vet J</addtitle><description>CD10 is an important cell marker in the diagnosis of acute lymphoblastic leukaemia and of breast myoepithelial (ME) cells in humans. The objective of this study was to assess the value of CD10 as a marker of canine ME cells using immunohistochemistry on routinely processed normal, dysplastic and neoplastic mammary tissue. Five different CD10 positive cell types were identified on the basis of cell morphology, pattern of immunoreactivity, and on the co-expression of additional cell lineage-specific markers.
Type 1 cells were typical fusiform cells with a ME cell phenotype (calponin- and cytokeratin [CK] 14-positive, CK8/18-negative). Type 2 cells were typical or atypical polyhedral cells with a luminal epithelial (LE) cell phenotype (calponin- and CK14-negative, CK8/18-positive). Type 3 cells had a type 1 phenotype with variable morphology, and type 4 were atypical neoplastic cells with a mixed ME/LE phenotype. Type 5 cells were typical fusiform cells with a stromal phenotype.
Type 1 cells were considered normal ME cells and were found in all sample types; type 2 cells were considered normal or neoplastic LE cells and were also found in all sample types; types 3 and 4 cells were restricted to tumour samples and to malignant tumours, respectively, and type 5 cells were found in all sample types, although predominantly in neoplastic tissue. The findings indicate that the CD10 antigen is a sensitive (although not specific) marker of canine ME cells in normal, dysplastic and neoplastic mammary tissue. Differences in the distribution and staining intensity of CD10-positive cells suggest a number of potential roles for this protein in the pathogenesis of canine mammary neoplasia.</description><subject>Adenoma - metabolism</subject><subject>Adenoma - veterinary</subject><subject>Animals</subject><subject>antigens</subject><subject>Biomarkers, Tumor</subject><subject>Calcium-Binding Proteins - genetics</subject><subject>Calcium-Binding Proteins - metabolism</subject><subject>Calponins</subject><subject>Canine</subject><subject>Carcinoma - metabolism</subject><subject>Carcinoma - veterinary</subject><subject>CD10</subject><subject>Dog Diseases - genetics</subject><subject>Dog Diseases - metabolism</subject><subject>Dogs</subject><subject>Female</subject><subject>Gene Expression Regulation - physiology</subject><subject>humans</subject><subject>immunohistochemistry</subject><subject>Keratin-14 - genetics</subject><subject>Keratin-14 - metabolism</subject><subject>leukemia</subject><subject>Mammary Neoplasms, Animal - metabolism</subject><subject>Mammary tumours</subject><subject>Microfilament Proteins - genetics</subject><subject>Microfilament Proteins - metabolism</subject><subject>Myoepithelium</subject><subject>Neprilysin - genetics</subject><subject>Neprilysin - metabolism</subject><subject>pathogenesis</subject><subject>phenotype</subject><subject>Staining and Labeling</subject><subject>stromal cells</subject><issn>1090-0233</issn><issn>1532-2971</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1r3DAQxUVJaT7af6CH1sdc7M6MbNmC5BA2n7DQQ7tnocjjVlt7vZG8gf3vK7NJjjkMMzzePB4_Ib4iFAiofqyL6XndFwRIBagCQH4QJ1hJyknXeJRu0JADSXksTmNcA4AuS_okjoka1NjQibhcRc7GLltcI2Q2ZjYbbPjHYdac3fgNJ2FI2j4b9iNv_fSXe2_7zHHfx8_iY2f7yF9e9plY3d78Xtzny593D4urZe5kA1NuNXZdK22lSkkNUFc5rctHoFpJllzrSjnFJRI2rWqUJFtXWjmtEC0ylvJMnB9yt2F82nGczODj3MBueNxFg9SU1NQKZisdrC6MMQbuzDb4ub9BMDM2szYzNjNjM6BMwpaevr3k7x4Hbt9eXjklw_eDobOjsX-Cj2b1KyVUkIZUNUdcHBycODx7DiY6zxvHrQ_sJtOO_r0G_wHhDYQk</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Sánchez-Céspedes, R.</creator><creator>Suárez-Bonnet, A.</creator><creator>Millán, Y.</creator><creator>Guil-Luna, S.</creator><creator>Reymundo, C.</creator><creator>Herráez, P.</creator><creator>Espinosa de los Monteros, A.</creator><creator>Martin de las Mulas, J.</creator><general>Elsevier Ltd</general><scope>FBQ</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>20130201</creationdate><title>Use of CD10 as a marker of canine mammary myoepithelial cells</title><author>Sánchez-Céspedes, R. ; Suárez-Bonnet, A. ; Millán, Y. ; Guil-Luna, S. ; Reymundo, C. ; Herráez, P. ; Espinosa de los Monteros, A. ; Martin de las Mulas, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-a91ffd3a56432802f5c994b02763e3e7956c6e41218d68632a7596c9611a1e143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenoma - metabolism</topic><topic>Adenoma - veterinary</topic><topic>Animals</topic><topic>antigens</topic><topic>Biomarkers, Tumor</topic><topic>Calcium-Binding Proteins - genetics</topic><topic>Calcium-Binding Proteins - metabolism</topic><topic>Calponins</topic><topic>Canine</topic><topic>Carcinoma - metabolism</topic><topic>Carcinoma - veterinary</topic><topic>CD10</topic><topic>Dog Diseases - genetics</topic><topic>Dog Diseases - metabolism</topic><topic>Dogs</topic><topic>Female</topic><topic>Gene Expression Regulation - physiology</topic><topic>humans</topic><topic>immunohistochemistry</topic><topic>Keratin-14 - genetics</topic><topic>Keratin-14 - metabolism</topic><topic>leukemia</topic><topic>Mammary Neoplasms, Animal - metabolism</topic><topic>Mammary tumours</topic><topic>Microfilament Proteins - genetics</topic><topic>Microfilament Proteins - metabolism</topic><topic>Myoepithelium</topic><topic>Neprilysin - genetics</topic><topic>Neprilysin - metabolism</topic><topic>pathogenesis</topic><topic>phenotype</topic><topic>Staining and Labeling</topic><topic>stromal cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sánchez-Céspedes, R.</creatorcontrib><creatorcontrib>Suárez-Bonnet, A.</creatorcontrib><creatorcontrib>Millán, Y.</creatorcontrib><creatorcontrib>Guil-Luna, S.</creatorcontrib><creatorcontrib>Reymundo, C.</creatorcontrib><creatorcontrib>Herráez, P.</creatorcontrib><creatorcontrib>Espinosa de los Monteros, A.</creatorcontrib><creatorcontrib>Martin de las Mulas, J.</creatorcontrib><collection>AGRIS</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 veterinary journal (1997)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sánchez-Céspedes, R.</au><au>Suárez-Bonnet, A.</au><au>Millán, Y.</au><au>Guil-Luna, S.</au><au>Reymundo, C.</au><au>Herráez, P.</au><au>Espinosa de los Monteros, A.</au><au>Martin de las Mulas, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of CD10 as a marker of canine mammary myoepithelial cells</atitle><jtitle>The veterinary journal (1997)</jtitle><addtitle>Vet J</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>195</volume><issue>2</issue><spage>192</spage><epage>199</epage><pages>192-199</pages><issn>1090-0233</issn><eissn>1532-2971</eissn><abstract>CD10 is an important cell marker in the diagnosis of acute lymphoblastic leukaemia and of breast myoepithelial (ME) cells in humans. The objective of this study was to assess the value of CD10 as a marker of canine ME cells using immunohistochemistry on routinely processed normal, dysplastic and neoplastic mammary tissue. Five different CD10 positive cell types were identified on the basis of cell morphology, pattern of immunoreactivity, and on the co-expression of additional cell lineage-specific markers.
Type 1 cells were typical fusiform cells with a ME cell phenotype (calponin- and cytokeratin [CK] 14-positive, CK8/18-negative). Type 2 cells were typical or atypical polyhedral cells with a luminal epithelial (LE) cell phenotype (calponin- and CK14-negative, CK8/18-positive). Type 3 cells had a type 1 phenotype with variable morphology, and type 4 were atypical neoplastic cells with a mixed ME/LE phenotype. Type 5 cells were typical fusiform cells with a stromal phenotype.
Type 1 cells were considered normal ME cells and were found in all sample types; type 2 cells were considered normal or neoplastic LE cells and were also found in all sample types; types 3 and 4 cells were restricted to tumour samples and to malignant tumours, respectively, and type 5 cells were found in all sample types, although predominantly in neoplastic tissue. The findings indicate that the CD10 antigen is a sensitive (although not specific) marker of canine ME cells in normal, dysplastic and neoplastic mammary tissue. Differences in the distribution and staining intensity of CD10-positive cells suggest a number of potential roles for this protein in the pathogenesis of canine mammary neoplasia.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>22819182</pmid><doi>10.1016/j.tvjl.2012.06.003</doi><tpages>8</tpages></addata></record> |
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subjects | Adenoma - metabolism Adenoma - veterinary Animals antigens Biomarkers, Tumor Calcium-Binding Proteins - genetics Calcium-Binding Proteins - metabolism Calponins Canine Carcinoma - metabolism Carcinoma - veterinary CD10 Dog Diseases - genetics Dog Diseases - metabolism Dogs Female Gene Expression Regulation - physiology humans immunohistochemistry Keratin-14 - genetics Keratin-14 - metabolism leukemia Mammary Neoplasms, Animal - metabolism Mammary tumours Microfilament Proteins - genetics Microfilament Proteins - metabolism Myoepithelium Neprilysin - genetics Neprilysin - metabolism pathogenesis phenotype Staining and Labeling stromal cells |
title | Use of CD10 as a marker of canine mammary myoepithelial cells |
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