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The cellular composition of adenoid cystic carcinoma. An immunohistochemical study
To investigate the cellular differentiation of adenoid cystic carcinomas (ACC), a comparative immunohistochemical study of 12 normal salivary glands and eight specimens of ACC was performed. Antibodies were used against S100 protein (S), keratins (K) of various molecular weights, vimentin (V), muscl...
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Published in: | Cancer 1987-10, Vol.60 (7), p.1589-1598 |
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description | To investigate the cellular differentiation of adenoid cystic carcinomas (ACC), a comparative immunohistochemical study of 12 normal salivary glands and eight specimens of ACC was performed. Antibodies were used against S100 protein (S), keratins (K) of various molecular weights, vimentin (V), muscle‐specific actin (A), epithelial‐membrane antigen, human milk fat globules, and collagen type IV. A panel of four of these antibodies (SKVA) was identified as the most helpful in characterizing cells in normal salivary glands and ACC. The immunophenotypes depended on the histologic patterns of ACC. Cells in morphologically recognizable duct structures in the cribriform and trabecular areas expressed a phenotype similar to that of the intercalated duct. Cell layers around pseudocysts and occasional cellular islands had an immunophenotype suggesting myoepithelial‐cell differentiation. The most clear cut epithelial/myoepithelial bilaminar differentiation was present in areas with a trabecular pattern, in which the layers facing the stroma and the central ductal elements had SKVA phenotypes of myoepithelial and ductal differentiation, respectively. In areas with a reticular pattern, most of the cells showed ductal differentiation. Many of the cells in the cribriform and basaloid regions were immunophenotypically undifferentiated. These results indicate that ACC consists of undifferentiated cells and of cells that are differentiating toward ducts, predominantly intercalated ducts, and toward myoepithelium. These findings support previous observations by electron microscope. |
doi_str_mv | 10.1002/1097-0142(19871001)60:7<1589::AID-CNCR2820600729>3.0.CO;2-U |
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An immunohistochemical study</title><source>EZB Electronic Journals Library</source><creator>Azumi, Norio ; Battifora, Hector</creator><creatorcontrib>Azumi, Norio ; Battifora, Hector</creatorcontrib><description>To investigate the cellular differentiation of adenoid cystic carcinomas (ACC), a comparative immunohistochemical study of 12 normal salivary glands and eight specimens of ACC was performed. Antibodies were used against S100 protein (S), keratins (K) of various molecular weights, vimentin (V), muscle‐specific actin (A), epithelial‐membrane antigen, human milk fat globules, and collagen type IV. A panel of four of these antibodies (SKVA) was identified as the most helpful in characterizing cells in normal salivary glands and ACC. The immunophenotypes depended on the histologic patterns of ACC. Cells in morphologically recognizable duct structures in the cribriform and trabecular areas expressed a phenotype similar to that of the intercalated duct. Cell layers around pseudocysts and occasional cellular islands had an immunophenotype suggesting myoepithelial‐cell differentiation. The most clear cut epithelial/myoepithelial bilaminar differentiation was present in areas with a trabecular pattern, in which the layers facing the stroma and the central ductal elements had SKVA phenotypes of myoepithelial and ductal differentiation, respectively. In areas with a reticular pattern, most of the cells showed ductal differentiation. Many of the cells in the cribriform and basaloid regions were immunophenotypically undifferentiated. These results indicate that ACC consists of undifferentiated cells and of cells that are differentiating toward ducts, predominantly intercalated ducts, and toward myoepithelium. These findings support previous observations by electron microscope.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19871001)60:7<1589::AID-CNCR2820600729>3.0.CO;2-U</identifier><identifier>PMID: 2441847</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Actins - analysis ; Antibodies ; Biological and medical sciences ; Breast Neoplasms - pathology ; Bronchial Neoplasms - pathology ; Carcinoma, Adenoid Cystic - pathology ; Cell Differentiation ; Collagen - analysis ; Histocytochemistry ; Keratins - analysis ; Lymphatic Metastasis ; Medical sciences ; Membrane Proteins - analysis ; Molecular Weight ; Mucin-1 ; Otorhinolaryngology. Stomatology ; Phenotype ; S100 Proteins - analysis ; Salivary Gland Neoplasms - pathology ; Salivary Glands - pathology ; Skin Neoplasms - pathology ; Submandibular Gland Neoplasms - pathology ; Tumors ; Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology ; Vimentin - analysis</subject><ispartof>Cancer, 1987-10, Vol.60 (7), p.1589-1598</ispartof><rights>Copyright © 1987 American Cancer Society</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5649-33587713797287307c403363bc255fa28468187ca0b33ca9aea73b15db1b80ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7389706$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2441847$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Azumi, Norio</creatorcontrib><creatorcontrib>Battifora, Hector</creatorcontrib><title>The cellular composition of adenoid cystic carcinoma. An immunohistochemical study</title><title>Cancer</title><addtitle>Cancer</addtitle><description>To investigate the cellular differentiation of adenoid cystic carcinomas (ACC), a comparative immunohistochemical study of 12 normal salivary glands and eight specimens of ACC was performed. Antibodies were used against S100 protein (S), keratins (K) of various molecular weights, vimentin (V), muscle‐specific actin (A), epithelial‐membrane antigen, human milk fat globules, and collagen type IV. A panel of four of these antibodies (SKVA) was identified as the most helpful in characterizing cells in normal salivary glands and ACC. The immunophenotypes depended on the histologic patterns of ACC. Cells in morphologically recognizable duct structures in the cribriform and trabecular areas expressed a phenotype similar to that of the intercalated duct. Cell layers around pseudocysts and occasional cellular islands had an immunophenotype suggesting myoepithelial‐cell differentiation. The most clear cut epithelial/myoepithelial bilaminar differentiation was present in areas with a trabecular pattern, in which the layers facing the stroma and the central ductal elements had SKVA phenotypes of myoepithelial and ductal differentiation, respectively. In areas with a reticular pattern, most of the cells showed ductal differentiation. Many of the cells in the cribriform and basaloid regions were immunophenotypically undifferentiated. These results indicate that ACC consists of undifferentiated cells and of cells that are differentiating toward ducts, predominantly intercalated ducts, and toward myoepithelium. These findings support previous observations by electron microscope.</description><subject>Actins - analysis</subject><subject>Antibodies</subject><subject>Biological and medical sciences</subject><subject>Breast Neoplasms - pathology</subject><subject>Bronchial Neoplasms - pathology</subject><subject>Carcinoma, Adenoid Cystic - pathology</subject><subject>Cell Differentiation</subject><subject>Collagen - analysis</subject><subject>Histocytochemistry</subject><subject>Keratins - analysis</subject><subject>Lymphatic Metastasis</subject><subject>Medical sciences</subject><subject>Membrane Proteins - analysis</subject><subject>Molecular Weight</subject><subject>Mucin-1</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Phenotype</subject><subject>S100 Proteins - analysis</subject><subject>Salivary Gland Neoplasms - pathology</subject><subject>Salivary Glands - pathology</subject><subject>Skin Neoplasms - pathology</subject><subject>Submandibular Gland Neoplasms - pathology</subject><subject>Tumors</subject><subject>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</subject><subject>Vimentin - analysis</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNqVkF2L1DAYhYMo67j6E4ReiLgXHd989U1nRRjq18LiwLIDghchTVMm0jZj07LMv7dlxgG9ELwK5Dw5nDyEFBSWFIC9pZBjClSwNzRXOF3RqwxW-I5Kla9W65sPafG1uGOKQQaALH_Pl7AsNtcs3T4ii_Prx2QBACqVgn97Sp7F-ANmXPILcsGEoErggtzd71xiXdOMjekTG9p9iH7woUtCnZjKdcFXiT3EwdvEmt76LrRmmay7xLft2IWdj0OwO9d6a5okDmN1eE6e1KaJ7sXpvCTbTx_viy_p7ebzTbG-Ta3MRJ5yLhUi5ZgjU8gBrQDOM15aJmVtmBKZogqtgZJza3LjDPKSyqqkpYLS8Evy-ti778PP0cVBtz7OXzGdC2PUiJkUAtkEfj-Ctg8x9q7W-963pj9oCno2rmdnenamfxvXGWjUs3GtJ-P6T-Oaa9DFRjO9ndpfnmaMZeuqc_dJ8ZS_OuUmTo7q3nTWxzOGXOUI2YTVR-zBN-7wfwv_OfCvhP8CUHuqVw</recordid><startdate>19871001</startdate><enddate>19871001</enddate><creator>Azumi, Norio</creator><creator>Battifora, Hector</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><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>19871001</creationdate><title>The cellular composition of adenoid cystic carcinoma. An immunohistochemical study</title><author>Azumi, Norio ; Battifora, Hector</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5649-33587713797287307c403363bc255fa28468187ca0b33ca9aea73b15db1b80ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Actins - analysis</topic><topic>Antibodies</topic><topic>Biological and medical sciences</topic><topic>Breast Neoplasms - pathology</topic><topic>Bronchial Neoplasms - pathology</topic><topic>Carcinoma, Adenoid Cystic - pathology</topic><topic>Cell Differentiation</topic><topic>Collagen - analysis</topic><topic>Histocytochemistry</topic><topic>Keratins - analysis</topic><topic>Lymphatic Metastasis</topic><topic>Medical sciences</topic><topic>Membrane Proteins - analysis</topic><topic>Molecular Weight</topic><topic>Mucin-1</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Phenotype</topic><topic>S100 Proteins - analysis</topic><topic>Salivary Gland Neoplasms - pathology</topic><topic>Salivary Glands - pathology</topic><topic>Skin Neoplasms - pathology</topic><topic>Submandibular Gland Neoplasms - pathology</topic><topic>Tumors</topic><topic>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</topic><topic>Vimentin - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Azumi, Norio</creatorcontrib><creatorcontrib>Battifora, Hector</creatorcontrib><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>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Azumi, Norio</au><au>Battifora, Hector</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The cellular composition of adenoid cystic carcinoma. An immunohistochemical study</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1987-10-01</date><risdate>1987</risdate><volume>60</volume><issue>7</issue><spage>1589</spage><epage>1598</epage><pages>1589-1598</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>To investigate the cellular differentiation of adenoid cystic carcinomas (ACC), a comparative immunohistochemical study of 12 normal salivary glands and eight specimens of ACC was performed. Antibodies were used against S100 protein (S), keratins (K) of various molecular weights, vimentin (V), muscle‐specific actin (A), epithelial‐membrane antigen, human milk fat globules, and collagen type IV. A panel of four of these antibodies (SKVA) was identified as the most helpful in characterizing cells in normal salivary glands and ACC. The immunophenotypes depended on the histologic patterns of ACC. Cells in morphologically recognizable duct structures in the cribriform and trabecular areas expressed a phenotype similar to that of the intercalated duct. Cell layers around pseudocysts and occasional cellular islands had an immunophenotype suggesting myoepithelial‐cell differentiation. The most clear cut epithelial/myoepithelial bilaminar differentiation was present in areas with a trabecular pattern, in which the layers facing the stroma and the central ductal elements had SKVA phenotypes of myoepithelial and ductal differentiation, respectively. In areas with a reticular pattern, most of the cells showed ductal differentiation. Many of the cells in the cribriform and basaloid regions were immunophenotypically undifferentiated. These results indicate that ACC consists of undifferentiated cells and of cells that are differentiating toward ducts, predominantly intercalated ducts, and toward myoepithelium. These findings support previous observations by electron microscope.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2441847</pmid><doi>10.1002/1097-0142(19871001)60:7<1589::AID-CNCR2820600729>3.0.CO;2-U</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actins - analysis Antibodies Biological and medical sciences Breast Neoplasms - pathology Bronchial Neoplasms - pathology Carcinoma, Adenoid Cystic - pathology Cell Differentiation Collagen - analysis Histocytochemistry Keratins - analysis Lymphatic Metastasis Medical sciences Membrane Proteins - analysis Molecular Weight Mucin-1 Otorhinolaryngology. Stomatology Phenotype S100 Proteins - analysis Salivary Gland Neoplasms - pathology Salivary Glands - pathology Skin Neoplasms - pathology Submandibular Gland Neoplasms - pathology Tumors Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology Vimentin - analysis |
title | The cellular composition of adenoid cystic carcinoma. An immunohistochemical study |
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