The complement regulatory proteins CD46 and CD59, but not CD55, are highly expressed by glandular epithelium of human breast and colorectal tumour tissues
Three of the proteins protecting cells from autologous lysis by complement are: membrane cofactor protein (MCP; CD46), an inhibitor of the membrane attack complex formation (CD59), and decay accelerating factor (DAF; CD55). We have investigated the expression of these proteins in breast and colorect...
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description | Three of the proteins protecting cells from autologous lysis by complement are: membrane cofactor protein (MCP; CD46), an inhibitor of the membrane attack complex formation (CD59), and decay accelerating factor (DAF; CD55). We have investigated the expression of these proteins in breast and colorectal carcinoma by immunohistochemistry and immunoblotting of breast tissue for CD46. CD46 was consistently and strongly expressed in the epithelial compartment in 26/28 ductal carcinomas of the breast, 9/9 fibroadenomas, and 9/11 cases of control non‐neoplastic breast tissue. CD59 showed a similar degree of expression in the fibroadenomas (9/9), but was less strongly expressed in carcinomatous (22/28) and control (5/11) tissues. In marked contrast, no CD55 expression was detected in tissue from 15 ductal carcinomas. Immunoblotting of breast tissue for CD46 showed the same size of the molecule as for lymphocytes. It had however considerably stronger expression in tumour tissue than in non‐neoplastic tissue. CD46 and CD59 were either lacking or only weakly expressed in the epithelial component of control colorectal mucosa: 2/15 and 5/15, respectively. In contrast, tissue samples from colorectal adenocarcinomas showed clear staining for both CD59 (10/18) and, more markedly, CD46 (15/18). There was no association between the pattern or intensity of CD46 and CD59 expression and tumour differentiation. As the complement regulatory proteins CD46 and CD59 are also strongly expressed by trophoblast at the feto‐maternal tissue interface, these results support the concept that similar mechanisms are employed both by the genetically dissimilar fetus and certain tumours to evade immune attack by their host. |
doi_str_mv | 10.1111/j.1699-0463.1998.tb00233.x |
format | Article |
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M. ; HARRINGTON, P. M. ; JOHNSON, P. M.</creator><creatorcontrib>THORSTEINSSON, L. ; O'DOWD, G. M. ; HARRINGTON, P. M. ; JOHNSON, P. M.</creatorcontrib><description>Three of the proteins protecting cells from autologous lysis by complement are: membrane cofactor protein (MCP; CD46), an inhibitor of the membrane attack complex formation (CD59), and decay accelerating factor (DAF; CD55). We have investigated the expression of these proteins in breast and colorectal carcinoma by immunohistochemistry and immunoblotting of breast tissue for CD46. CD46 was consistently and strongly expressed in the epithelial compartment in 26/28 ductal carcinomas of the breast, 9/9 fibroadenomas, and 9/11 cases of control non‐neoplastic breast tissue. CD59 showed a similar degree of expression in the fibroadenomas (9/9), but was less strongly expressed in carcinomatous (22/28) and control (5/11) tissues. In marked contrast, no CD55 expression was detected in tissue from 15 ductal carcinomas. Immunoblotting of breast tissue for CD46 showed the same size of the molecule as for lymphocytes. It had however considerably stronger expression in tumour tissue than in non‐neoplastic tissue. CD46 and CD59 were either lacking or only weakly expressed in the epithelial component of control colorectal mucosa: 2/15 and 5/15, respectively. In contrast, tissue samples from colorectal adenocarcinomas showed clear staining for both CD59 (10/18) and, more markedly, CD46 (15/18). There was no association between the pattern or intensity of CD46 and CD59 expression and tumour differentiation. As the complement regulatory proteins CD46 and CD59 are also strongly expressed by trophoblast at the feto‐maternal tissue interface, these results support the concept that similar mechanisms are employed both by the genetically dissimilar fetus and certain tumours to evade immune attack by their host.</description><identifier>ISSN: 0903-4641</identifier><identifier>EISSN: 1600-0463</identifier><identifier>DOI: 10.1111/j.1699-0463.1998.tb00233.x</identifier><identifier>PMID: 9808413</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenocarcinoma - immunology ; Adult ; Aged ; Antigens, CD - analysis ; Antigens, CD - blood ; Biological and medical sciences ; Blotting, Western ; Breast - immunology ; Breast and colorectal tumours ; Breast Neoplasms - immunology ; Carcinoma, Ductal, Breast - immunology ; CD46 ; CD55 ; CD55 Antigens - analysis ; CD59 Antigens - analysis ; Colorectal Neoplasms - immunology ; Complement System Proteins ; decay accelerating factor (DAF ; Enzyme-Linked Immunosorbent Assay ; Epithelial Cells - immunology ; Female ; Fibroadenoma - immunology ; Gynecology. Andrology. Obstetrics ; HLA Antigens - analysis ; Humans ; Immunohistochemistry ; inhibitor of membrane attack complex formation (CD59) ; Intestinal Mucosa - immunology ; Lymphocytes - immunology ; Mammary gland diseases ; Medical sciences ; Membrane Cofactor Protein ; membrane cofactor protein (MCP ; Membrane Glycoproteins - analysis ; Membrane Glycoproteins - blood ; Middle Aged ; regulators of complement activation (RCA) ; Stromal Cells - immunology ; Tumors</subject><ispartof>APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 1998-09, Vol.106 (7-12), p.869-878</ispartof><rights>1998 APMIS</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4369-6f3970258bf0862df8cf531d73e8250042c5bd0d6f64868f160011e278581b193</citedby><cites>FETCH-LOGICAL-c4369-6f3970258bf0862df8cf531d73e8250042c5bd0d6f64868f160011e278581b193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1699-0463.1998.tb00233.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1699-0463.1998.tb00233.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1595966$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9808413$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>THORSTEINSSON, L.</creatorcontrib><creatorcontrib>O'DOWD, G. M.</creatorcontrib><creatorcontrib>HARRINGTON, P. M.</creatorcontrib><creatorcontrib>JOHNSON, P. M.</creatorcontrib><title>The complement regulatory proteins CD46 and CD59, but not CD55, are highly expressed by glandular epithelium of human breast and colorectal tumour tissues</title><title>APMIS : acta pathologica, microbiologica et immunologica Scandinavica</title><addtitle>APMIS</addtitle><description>Three of the proteins protecting cells from autologous lysis by complement are: membrane cofactor protein (MCP; CD46), an inhibitor of the membrane attack complex formation (CD59), and decay accelerating factor (DAF; CD55). We have investigated the expression of these proteins in breast and colorectal carcinoma by immunohistochemistry and immunoblotting of breast tissue for CD46. CD46 was consistently and strongly expressed in the epithelial compartment in 26/28 ductal carcinomas of the breast, 9/9 fibroadenomas, and 9/11 cases of control non‐neoplastic breast tissue. CD59 showed a similar degree of expression in the fibroadenomas (9/9), but was less strongly expressed in carcinomatous (22/28) and control (5/11) tissues. In marked contrast, no CD55 expression was detected in tissue from 15 ductal carcinomas. Immunoblotting of breast tissue for CD46 showed the same size of the molecule as for lymphocytes. It had however considerably stronger expression in tumour tissue than in non‐neoplastic tissue. CD46 and CD59 were either lacking or only weakly expressed in the epithelial component of control colorectal mucosa: 2/15 and 5/15, respectively. In contrast, tissue samples from colorectal adenocarcinomas showed clear staining for both CD59 (10/18) and, more markedly, CD46 (15/18). There was no association between the pattern or intensity of CD46 and CD59 expression and tumour differentiation. As the complement regulatory proteins CD46 and CD59 are also strongly expressed by trophoblast at the feto‐maternal tissue interface, these results support the concept that similar mechanisms are employed both by the genetically dissimilar fetus and certain tumours to evade immune attack by their host.</description><subject>Adenocarcinoma - immunology</subject><subject>Adult</subject><subject>Aged</subject><subject>Antigens, CD - analysis</subject><subject>Antigens, CD - blood</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Breast - immunology</subject><subject>Breast and colorectal tumours</subject><subject>Breast Neoplasms - immunology</subject><subject>Carcinoma, Ductal, Breast - immunology</subject><subject>CD46</subject><subject>CD55</subject><subject>CD55 Antigens - analysis</subject><subject>CD59 Antigens - analysis</subject><subject>Colorectal Neoplasms - immunology</subject><subject>Complement System Proteins</subject><subject>decay accelerating factor (DAF</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Epithelial Cells - immunology</subject><subject>Female</subject><subject>Fibroadenoma - immunology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>HLA Antigens - analysis</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>inhibitor of membrane attack complex formation (CD59)</subject><subject>Intestinal Mucosa - immunology</subject><subject>Lymphocytes - immunology</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Membrane Cofactor Protein</subject><subject>membrane cofactor protein (MCP</subject><subject>Membrane Glycoproteins - analysis</subject><subject>Membrane Glycoproteins - blood</subject><subject>Middle Aged</subject><subject>regulators of complement activation (RCA)</subject><subject>Stromal Cells - immunology</subject><subject>Tumors</subject><issn>0903-4641</issn><issn>1600-0463</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUcuO1DAQtBBoGQY-AclCiNMm2HHs2ByQloFdkJanFnG0nKQzk8F5YDti8it8Lc7OaDnji92q7mpXFULPKElpPC_3KRVKJSQXLKVKyTSUhGSMpYd7aEUFIbfQfbQiirAkFzl9iB55vyeEZlIUZ-hMSSJzylboz80OcDV0o4UO-oAdbCdrwuBmPLohQNt7vHmbC2z6Oj64OsflFHA_hKXi59g4wLt2u7MzhsPowHuocTnjrY0TkcphGNuwA9tOHR4avJs60-PSgfHhlrQa7OCgCsbiMHXD5HBovZ_AP0YPGmM9PDnda_T98t3N5n1y_fnqw-biOqlyJlQiGqYKknFZNkSKrG5k1XBG64KBzDgheVbxsia1aEQuhWwWfyiFrJBc0pIqtkYvjrxR8K-4N-iu9RXYKACGyeuCEJaT6NYavTo2Vm7w3kGjR9d2xs2aEr0Eo_d6CUYv7uslGH0KRh_i8NPTlqnsoL4bPSUR8ecn3PjK2MaZvmr9vw1ccSVEbHt9bPvdWpj_4wP64stHKRa1yZGg9QEOdwTG_dSiYAXXPz5d6ZxfZl-_vdloxv4C2Aa5eQ</recordid><startdate>19980901</startdate><enddate>19980901</enddate><creator>THORSTEINSSON, L.</creator><creator>O'DOWD, G. M.</creator><creator>HARRINGTON, P. M.</creator><creator>JOHNSON, P. M.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</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>19980901</creationdate><title>The complement regulatory proteins CD46 and CD59, but not CD55, are highly expressed by glandular epithelium of human breast and colorectal tumour tissues</title><author>THORSTEINSSON, L. ; O'DOWD, G. M. ; HARRINGTON, P. M. ; JOHNSON, P. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4369-6f3970258bf0862df8cf531d73e8250042c5bd0d6f64868f160011e278581b193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adenocarcinoma - immunology</topic><topic>Adult</topic><topic>Aged</topic><topic>Antigens, CD - analysis</topic><topic>Antigens, CD - blood</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Breast - immunology</topic><topic>Breast and colorectal tumours</topic><topic>Breast Neoplasms - immunology</topic><topic>Carcinoma, Ductal, Breast - immunology</topic><topic>CD46</topic><topic>CD55</topic><topic>CD55 Antigens - analysis</topic><topic>CD59 Antigens - analysis</topic><topic>Colorectal Neoplasms - immunology</topic><topic>Complement System Proteins</topic><topic>decay accelerating factor (DAF</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Epithelial Cells - immunology</topic><topic>Female</topic><topic>Fibroadenoma - immunology</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>HLA Antigens - analysis</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>inhibitor of membrane attack complex formation (CD59)</topic><topic>Intestinal Mucosa - immunology</topic><topic>Lymphocytes - immunology</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Membrane Cofactor Protein</topic><topic>membrane cofactor protein (MCP</topic><topic>Membrane Glycoproteins - analysis</topic><topic>Membrane Glycoproteins - blood</topic><topic>Middle Aged</topic><topic>regulators of complement activation (RCA)</topic><topic>Stromal Cells - immunology</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>THORSTEINSSON, L.</creatorcontrib><creatorcontrib>O'DOWD, G. M.</creatorcontrib><creatorcontrib>HARRINGTON, P. M.</creatorcontrib><creatorcontrib>JOHNSON, P. M.</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>APMIS : acta pathologica, microbiologica et immunologica Scandinavica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>THORSTEINSSON, L.</au><au>O'DOWD, G. M.</au><au>HARRINGTON, P. M.</au><au>JOHNSON, P. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The complement regulatory proteins CD46 and CD59, but not CD55, are highly expressed by glandular epithelium of human breast and colorectal tumour tissues</atitle><jtitle>APMIS : acta pathologica, microbiologica et immunologica Scandinavica</jtitle><addtitle>APMIS</addtitle><date>1998-09-01</date><risdate>1998</risdate><volume>106</volume><issue>7-12</issue><spage>869</spage><epage>878</epage><pages>869-878</pages><issn>0903-4641</issn><eissn>1600-0463</eissn><abstract>Three of the proteins protecting cells from autologous lysis by complement are: membrane cofactor protein (MCP; CD46), an inhibitor of the membrane attack complex formation (CD59), and decay accelerating factor (DAF; CD55). We have investigated the expression of these proteins in breast and colorectal carcinoma by immunohistochemistry and immunoblotting of breast tissue for CD46. CD46 was consistently and strongly expressed in the epithelial compartment in 26/28 ductal carcinomas of the breast, 9/9 fibroadenomas, and 9/11 cases of control non‐neoplastic breast tissue. CD59 showed a similar degree of expression in the fibroadenomas (9/9), but was less strongly expressed in carcinomatous (22/28) and control (5/11) tissues. In marked contrast, no CD55 expression was detected in tissue from 15 ductal carcinomas. Immunoblotting of breast tissue for CD46 showed the same size of the molecule as for lymphocytes. It had however considerably stronger expression in tumour tissue than in non‐neoplastic tissue. CD46 and CD59 were either lacking or only weakly expressed in the epithelial component of control colorectal mucosa: 2/15 and 5/15, respectively. In contrast, tissue samples from colorectal adenocarcinomas showed clear staining for both CD59 (10/18) and, more markedly, CD46 (15/18). There was no association between the pattern or intensity of CD46 and CD59 expression and tumour differentiation. As the complement regulatory proteins CD46 and CD59 are also strongly expressed by trophoblast at the feto‐maternal tissue interface, these results support the concept that similar mechanisms are employed both by the genetically dissimilar fetus and certain tumours to evade immune attack by their host.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>9808413</pmid><doi>10.1111/j.1699-0463.1998.tb00233.x</doi><tpages>10</tpages></addata></record> |
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subjects | Adenocarcinoma - immunology Adult Aged Antigens, CD - analysis Antigens, CD - blood Biological and medical sciences Blotting, Western Breast - immunology Breast and colorectal tumours Breast Neoplasms - immunology Carcinoma, Ductal, Breast - immunology CD46 CD55 CD55 Antigens - analysis CD59 Antigens - analysis Colorectal Neoplasms - immunology Complement System Proteins decay accelerating factor (DAF Enzyme-Linked Immunosorbent Assay Epithelial Cells - immunology Female Fibroadenoma - immunology Gynecology. Andrology. Obstetrics HLA Antigens - analysis Humans Immunohistochemistry inhibitor of membrane attack complex formation (CD59) Intestinal Mucosa - immunology Lymphocytes - immunology Mammary gland diseases Medical sciences Membrane Cofactor Protein membrane cofactor protein (MCP Membrane Glycoproteins - analysis Membrane Glycoproteins - blood Middle Aged regulators of complement activation (RCA) Stromal Cells - immunology Tumors |
title | The complement regulatory proteins CD46 and CD59, but not CD55, are highly expressed by glandular epithelium of human breast and colorectal tumour tissues |
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