Staining pattern of specific and cross‐reacting Melan‐A antibodies: A comparative study on 15,840 samples from 133 human tumor types

The Melan‐A (melanocyte antigen) protein, also termed ‘melanoma antigen recognized by T cells 1’ (MART‐1) is a protein with unknown function whose expression is specific for the melanocyte lineage. Antibodies against Melan‐A are thus used for identifying melanocytic tumors, but some Melan‐A antibodi...

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Veröffentlicht in:APMIS : acta pathologica, microbiologica et immunologica Scandinavica microbiologica et immunologica Scandinavica, 2024-07, Vol.132 (7), p.479-491
Hauptverfasser: Boroojerdi, Shiva, Weidemann, Sören, Menz, Anne, Lennartz, Maximilian, Dwertmann Rico, Sebastian, Schlichter, Ria, Kind, Simon, Reiswich, Viktor, Viehweger, Florian, Bawahab, Ahmed Abdulwahab, Höflmeyer, Doris, Fraune, Christoph, Gorbokon, Natalia, Luebke, Andreas M., Hube‐Magg, Claudia, Büscheck, Franziska, Krech, Till, Hinsch, Andrea, Jacobsen, Frank, Burandt, Eike, Sauter, Guido, Simon, Ronald, Kluth, Martina, Steurer, Stefan, Minner, Sarah, Marx, Andreas H., Bernreuther, Christian, Clauditz, Till S., Dum, David, Lebok, Patrick
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container_title APMIS : acta pathologica, microbiologica et immunologica Scandinavica
container_volume 132
creator Boroojerdi, Shiva
Weidemann, Sören
Menz, Anne
Lennartz, Maximilian
Dwertmann Rico, Sebastian
Schlichter, Ria
Kind, Simon
Reiswich, Viktor
Viehweger, Florian
Bawahab, Ahmed Abdulwahab
Höflmeyer, Doris
Fraune, Christoph
Gorbokon, Natalia
Luebke, Andreas M.
Hube‐Magg, Claudia
Büscheck, Franziska
Krech, Till
Hinsch, Andrea
Jacobsen, Frank
Burandt, Eike
Sauter, Guido
Simon, Ronald
Kluth, Martina
Steurer, Stefan
Minner, Sarah
Marx, Andreas H.
Bernreuther, Christian
Clauditz, Till S.
Dum, David
Lebok, Patrick
description The Melan‐A (melanocyte antigen) protein, also termed ‘melanoma antigen recognized by T cells 1’ (MART‐1) is a protein with unknown function whose expression is specific for the melanocyte lineage. Antibodies against Melan‐A are thus used for identifying melanocytic tumors, but some Melan‐A antibodies show an additional – diagnostically useful – cross‐reactivity against an unspecified protein involved in corticosteroid hormone synthesis. To comprehensively compare the staining patterns of a specific and a cross‐reactive Melan‐A antibody in normal and neoplastic tissues, tissue microarrays containing 15,840 samples from 133 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types were analyzed by immunohistochemistry. For the Melan‐A‐specific antibody ‘Melan‐A specific’ (MSVA‐900M), Melan‐A positivity was seen in 96.0% of 25 benign nevi, 93.0% of 40 primary and 86.7% of 75 metastatic melanomas, 82.4% of 85 renal angiomyolipomas as well as 96.4% of 84 neurofibromas, 2.2% of 46 granular cell tumors, 1.0% of 104 schwannomas, and 1.1% of 87 leiomyosarcomas. The cross‐reactive antibody ‘Melan‐A+' (MSVA‐901M+) stained 98.1% of the tumors stained by ‘Melan‐A specific’. In addition, high positivity rates were seen in sex‐cord‐stroma tumors of the ovary (35.3%–100%) and the testis (86.7%) as well as for adrenocortical neoplasms (76.3%–83.0%). Only nine further tumor groups showed Melan‐A+ staining, including five different categories of urothelial carcinomas. Our data provide a comprehensive overview on the staining patterns of specific and cross‐reactive Melan‐A antibodies. The data demonstrate that both antibodies are highly useful for their specific purpose. It is important for pathologists to distinguish these two Melan‐A antibody subtypes for their daily work.
doi_str_mv 10.1111/apm.13408
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Antibodies against Melan‐A are thus used for identifying melanocytic tumors, but some Melan‐A antibodies show an additional – diagnostically useful – cross‐reactivity against an unspecified protein involved in corticosteroid hormone synthesis. To comprehensively compare the staining patterns of a specific and a cross‐reactive Melan‐A antibody in normal and neoplastic tissues, tissue microarrays containing 15,840 samples from 133 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types were analyzed by immunohistochemistry. For the Melan‐A‐specific antibody ‘Melan‐A specific’ (MSVA‐900M), Melan‐A positivity was seen in 96.0% of 25 benign nevi, 93.0% of 40 primary and 86.7% of 75 metastatic melanomas, 82.4% of 85 renal angiomyolipomas as well as 96.4% of 84 neurofibromas, 2.2% of 46 granular cell tumors, 1.0% of 104 schwannomas, and 1.1% of 87 leiomyosarcomas. The cross‐reactive antibody ‘Melan‐A+' (MSVA‐901M+) stained 98.1% of the tumors stained by ‘Melan‐A specific’. In addition, high positivity rates were seen in sex‐cord‐stroma tumors of the ovary (35.3%–100%) and the testis (86.7%) as well as for adrenocortical neoplasms (76.3%–83.0%). Only nine further tumor groups showed Melan‐A+ staining, including five different categories of urothelial carcinomas. Our data provide a comprehensive overview on the staining patterns of specific and cross‐reactive Melan‐A antibodies. The data demonstrate that both antibodies are highly useful for their specific purpose. 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The cross‐reactive antibody ‘Melan‐A+' (MSVA‐901M+) stained 98.1% of the tumors stained by ‘Melan‐A specific’. In addition, high positivity rates were seen in sex‐cord‐stroma tumors of the ovary (35.3%–100%) and the testis (86.7%) as well as for adrenocortical neoplasms (76.3%–83.0%). Only nine further tumor groups showed Melan‐A+ staining, including five different categories of urothelial carcinomas. Our data provide a comprehensive overview on the staining patterns of specific and cross‐reactive Melan‐A antibodies. The data demonstrate that both antibodies are highly useful for their specific purpose. 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immunology</subject><subject>Neoplasms - pathology</subject><subject>Proteins</subject><subject>Staining</subject><subject>Stroma</subject><subject>Tissue Array Analysis</subject><subject>tissue microarray</subject><subject>Tumors</subject><subject>Urothelial carcinoma</subject><issn>0903-4641</issn><issn>1600-0463</issn><issn>1600-0463</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp10cFqFTEUBuAgir1WF76ABNwoOG0yyWQy7i7FVqFFQV0PJ5kzmjKZjElGuTuXLn1Gn8Tc3upCMJtA8vGTk5-Qx5yd8LJOYfEnXEim75ANV4xVTCpxl2xYx0QlleRH5EFK14zxWqv2PjkSum3aWuoN-fE-g5vd_IkukDPGmYaRpgWtG52lMA_UxpDSr-8_I4LNe3iFE8zlYFuuszNhcJhe0i21wS8QIbuvSFNehx0NM-XNCy0ZTeCXCRMdY_CUC0E_rx5mmlcfIs27BdNDcm-EKeGj2_2YfDx_9eHsdXX59uLN2fayskJqXYnOtDBI4KJWHW-Y5abmoGWtuVYDcGxN19WdbphWY601WGVMZ8GYEQyvURyTZ4fcJYYvK6bce5csTmUmDGvqBWuUUkIoWejTf-h1WONcXleUkrrVrNur5wd181ERx36JzkPc9Zz1-3r6Uk9_U0-xT24TV-Nx-Cv_9FHA6QF8cxPu_p_Ub99dHSJ_A8M1ml8</recordid><startdate>202407</startdate><enddate>202407</enddate><creator>Boroojerdi, Shiva</creator><creator>Weidemann, Sören</creator><creator>Menz, Anne</creator><creator>Lennartz, Maximilian</creator><creator>Dwertmann Rico, Sebastian</creator><creator>Schlichter, Ria</creator><creator>Kind, Simon</creator><creator>Reiswich, Viktor</creator><creator>Viehweger, Florian</creator><creator>Bawahab, Ahmed Abdulwahab</creator><creator>Höflmeyer, Doris</creator><creator>Fraune, Christoph</creator><creator>Gorbokon, Natalia</creator><creator>Luebke, Andreas M.</creator><creator>Hube‐Magg, Claudia</creator><creator>Büscheck, Franziska</creator><creator>Krech, Till</creator><creator>Hinsch, Andrea</creator><creator>Jacobsen, Frank</creator><creator>Burandt, Eike</creator><creator>Sauter, Guido</creator><creator>Simon, Ronald</creator><creator>Kluth, Martina</creator><creator>Steurer, Stefan</creator><creator>Minner, Sarah</creator><creator>Marx, Andreas H.</creator><creator>Bernreuther, Christian</creator><creator>Clauditz, Till S.</creator><creator>Dum, David</creator><creator>Lebok, Patrick</creator><general>Wiley Subscription Services, Inc</general><scope>24P</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>7QL</scope><scope>7T5</scope><scope>7T7</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7542-4340</orcidid><orcidid>https://orcid.org/0000-0002-5705-9084</orcidid><orcidid>https://orcid.org/0000-0003-0158-4258</orcidid><orcidid>https://orcid.org/0000-0002-1572-8200</orcidid><orcidid>https://orcid.org/0000-0003-3939-322X</orcidid></search><sort><creationdate>202407</creationdate><title>Staining pattern of specific and cross‐reacting Melan‐A antibodies: A comparative study on 15,840 samples from 133 human tumor types</title><author>Boroojerdi, Shiva ; Weidemann, Sören ; Menz, Anne ; Lennartz, Maximilian ; Dwertmann Rico, Sebastian ; Schlichter, Ria ; Kind, Simon ; Reiswich, Viktor ; Viehweger, Florian ; Bawahab, Ahmed Abdulwahab ; Höflmeyer, Doris ; Fraune, Christoph ; Gorbokon, Natalia ; Luebke, Andreas M. ; Hube‐Magg, Claudia ; Büscheck, Franziska ; Krech, Till ; Hinsch, Andrea ; Jacobsen, Frank ; Burandt, Eike ; Sauter, Guido ; Simon, Ronald ; Kluth, Martina ; Steurer, Stefan ; Minner, Sarah ; Marx, Andreas H. ; Bernreuther, Christian ; Clauditz, Till S. ; Dum, David ; Lebok, Patrick</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3488-39b7ad4a13269150c1b21a8428186da1e7b992985086f288ac6bb9cabbfab12e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antibodies</topic><topic>Antigens</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Biomarkers, Tumor - immunology</topic><topic>Comparative studies</topic><topic>Cross Reactions - immunology</topic><topic>Cross‐reactive antibody</topic><topic>diagnostic</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunohistochemistry - methods</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>MART-1 Antigen - analysis</topic><topic>MART-1 Antigen - immunology</topic><topic>Melanoma</topic><topic>Melanoma - diagnosis</topic><topic>Melanoma - immunology</topic><topic>Melanoma - pathology</topic><topic>Melan‐A</topic><topic>Metastases</topic><topic>Neoplasms</topic><topic>Neoplasms - diagnosis</topic><topic>Neoplasms - immunology</topic><topic>Neoplasms - pathology</topic><topic>Proteins</topic><topic>Staining</topic><topic>Stroma</topic><topic>Tissue Array Analysis</topic><topic>tissue microarray</topic><topic>Tumors</topic><topic>Urothelial carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boroojerdi, Shiva</creatorcontrib><creatorcontrib>Weidemann, Sören</creatorcontrib><creatorcontrib>Menz, Anne</creatorcontrib><creatorcontrib>Lennartz, Maximilian</creatorcontrib><creatorcontrib>Dwertmann Rico, Sebastian</creatorcontrib><creatorcontrib>Schlichter, Ria</creatorcontrib><creatorcontrib>Kind, Simon</creatorcontrib><creatorcontrib>Reiswich, Viktor</creatorcontrib><creatorcontrib>Viehweger, Florian</creatorcontrib><creatorcontrib>Bawahab, Ahmed Abdulwahab</creatorcontrib><creatorcontrib>Höflmeyer, Doris</creatorcontrib><creatorcontrib>Fraune, Christoph</creatorcontrib><creatorcontrib>Gorbokon, Natalia</creatorcontrib><creatorcontrib>Luebke, Andreas M.</creatorcontrib><creatorcontrib>Hube‐Magg, Claudia</creatorcontrib><creatorcontrib>Büscheck, Franziska</creatorcontrib><creatorcontrib>Krech, Till</creatorcontrib><creatorcontrib>Hinsch, Andrea</creatorcontrib><creatorcontrib>Jacobsen, Frank</creatorcontrib><creatorcontrib>Burandt, Eike</creatorcontrib><creatorcontrib>Sauter, Guido</creatorcontrib><creatorcontrib>Simon, Ronald</creatorcontrib><creatorcontrib>Kluth, Martina</creatorcontrib><creatorcontrib>Steurer, Stefan</creatorcontrib><creatorcontrib>Minner, Sarah</creatorcontrib><creatorcontrib>Marx, Andreas H.</creatorcontrib><creatorcontrib>Bernreuther, Christian</creatorcontrib><creatorcontrib>Clauditz, Till S.</creatorcontrib><creatorcontrib>Dum, David</creatorcontrib><creatorcontrib>Lebok, Patrick</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</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>Boroojerdi, Shiva</au><au>Weidemann, Sören</au><au>Menz, Anne</au><au>Lennartz, Maximilian</au><au>Dwertmann Rico, Sebastian</au><au>Schlichter, Ria</au><au>Kind, Simon</au><au>Reiswich, Viktor</au><au>Viehweger, Florian</au><au>Bawahab, Ahmed Abdulwahab</au><au>Höflmeyer, Doris</au><au>Fraune, Christoph</au><au>Gorbokon, Natalia</au><au>Luebke, Andreas M.</au><au>Hube‐Magg, Claudia</au><au>Büscheck, Franziska</au><au>Krech, Till</au><au>Hinsch, Andrea</au><au>Jacobsen, Frank</au><au>Burandt, Eike</au><au>Sauter, Guido</au><au>Simon, Ronald</au><au>Kluth, Martina</au><au>Steurer, Stefan</au><au>Minner, Sarah</au><au>Marx, Andreas H.</au><au>Bernreuther, Christian</au><au>Clauditz, Till S.</au><au>Dum, David</au><au>Lebok, Patrick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Staining pattern of specific and cross‐reacting Melan‐A antibodies: A comparative study on 15,840 samples from 133 human tumor types</atitle><jtitle>APMIS : acta pathologica, microbiologica et immunologica Scandinavica</jtitle><addtitle>APMIS</addtitle><date>2024-07</date><risdate>2024</risdate><volume>132</volume><issue>7</issue><spage>479</spage><epage>491</epage><pages>479-491</pages><issn>0903-4641</issn><issn>1600-0463</issn><eissn>1600-0463</eissn><abstract>The Melan‐A (melanocyte antigen) protein, also termed ‘melanoma antigen recognized by T cells 1’ (MART‐1) is a protein with unknown function whose expression is specific for the melanocyte lineage. Antibodies against Melan‐A are thus used for identifying melanocytic tumors, but some Melan‐A antibodies show an additional – diagnostically useful – cross‐reactivity against an unspecified protein involved in corticosteroid hormone synthesis. To comprehensively compare the staining patterns of a specific and a cross‐reactive Melan‐A antibody in normal and neoplastic tissues, tissue microarrays containing 15,840 samples from 133 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types were analyzed by immunohistochemistry. For the Melan‐A‐specific antibody ‘Melan‐A specific’ (MSVA‐900M), Melan‐A positivity was seen in 96.0% of 25 benign nevi, 93.0% of 40 primary and 86.7% of 75 metastatic melanomas, 82.4% of 85 renal angiomyolipomas as well as 96.4% of 84 neurofibromas, 2.2% of 46 granular cell tumors, 1.0% of 104 schwannomas, and 1.1% of 87 leiomyosarcomas. The cross‐reactive antibody ‘Melan‐A+' (MSVA‐901M+) stained 98.1% of the tumors stained by ‘Melan‐A specific’. In addition, high positivity rates were seen in sex‐cord‐stroma tumors of the ovary (35.3%–100%) and the testis (86.7%) as well as for adrenocortical neoplasms (76.3%–83.0%). Only nine further tumor groups showed Melan‐A+ staining, including five different categories of urothelial carcinomas. Our data provide a comprehensive overview on the staining patterns of specific and cross‐reactive Melan‐A antibodies. The data demonstrate that both antibodies are highly useful for their specific purpose. It is important for pathologists to distinguish these two Melan‐A antibody subtypes for their daily work.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38757248</pmid><doi>10.1111/apm.13408</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-7542-4340</orcidid><orcidid>https://orcid.org/0000-0002-5705-9084</orcidid><orcidid>https://orcid.org/0000-0003-0158-4258</orcidid><orcidid>https://orcid.org/0000-0002-1572-8200</orcidid><orcidid>https://orcid.org/0000-0003-3939-322X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Antibodies
Antigens
Biomarkers, Tumor - analysis
Biomarkers, Tumor - immunology
Comparative studies
Cross Reactions - immunology
Cross‐reactive antibody
diagnostic
Female
Humans
Immunohistochemistry
Immunohistochemistry - methods
Lymphocytes
Lymphocytes T
MART-1 Antigen - analysis
MART-1 Antigen - immunology
Melanoma
Melanoma - diagnosis
Melanoma - immunology
Melanoma - pathology
Melan‐A
Metastases
Neoplasms
Neoplasms - diagnosis
Neoplasms - immunology
Neoplasms - pathology
Proteins
Staining
Stroma
Tissue Array Analysis
tissue microarray
Tumors
Urothelial carcinoma
title Staining pattern of specific and cross‐reacting Melan‐A antibodies: A comparative study on 15,840 samples from 133 human tumor types
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