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Frequent overexpression of CADM1/IGSF4 in lung adenocarcinoma
We reported comprehensive screening for antigens (Ags) overexpressed on various carcinomas via isolation of human monoclonal antibodies (mAbs) that may be therapeutic in a previous paper (Proc. Natl. Acad. Sci. USA 105, 7287-7292, 2008). Twenty-one distinct Ags highly expressed on several carcinomas...
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Published in: | Biochemical and biophysical research communications 2009-06, Vol.383 (4), p.480-484 |
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creator | Kitamura, Yuka Kurosawa, Gene Tanaka, Miho Sumitomo, Mariko Muramatsu, Chiho Eguchi, Keiko Akahori, Yasushi Iba, Yoshitaka Tsuda, Hiroyuki Sugiura, Mototaka Hattori, Yoshinobu Kurosawa, Yoshikazu |
description | We reported comprehensive screening for antigens (Ags) overexpressed on various carcinomas via isolation of human monoclonal antibodies (mAbs) that may be therapeutic in a previous paper (Proc. Natl. Acad. Sci. USA 105, 7287-7292, 2008). Twenty-one distinct Ags highly expressed on several carcinomas were identified and 356 mAbs with unique sequences turned out to bind to one of the 21 Ags. Among them CADM1/IGSF4 which had been originally referred to as tumor suppressor lung cancer 1 (TSLC1) was included. Therefore we examined the expression of CADM1 in lung cancers in this study. Eight different anti CADM1 mAbs were used for immunohistochemical analysis of 29 fresh lung cancer specimens. Staining patterns were categorized to six groups based on the extent of positive staining and the localization of stained portions. While overexpression of CADM1 was observed on the cell surface of adenocarcinomas at a high frequency, around 60%, positive stainings were rarely observed on that of other lung carcinomas including squamous cell carcinomas. Moreover, some clones among the eight mAbs gave different staining patterns from those by the other clones against the same fresh specimen, suggesting presence of variant forms of CADM1 differentiated by mAbs. |
doi_str_mv | 10.1016/j.bbrc.2009.04.039 |
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Natl. Acad. Sci. USA 105, 7287-7292, 2008). Twenty-one distinct Ags highly expressed on several carcinomas were identified and 356 mAbs with unique sequences turned out to bind to one of the 21 Ags. Among them CADM1/IGSF4 which had been originally referred to as tumor suppressor lung cancer 1 (TSLC1) was included. Therefore we examined the expression of CADM1 in lung cancers in this study. Eight different anti CADM1 mAbs were used for immunohistochemical analysis of 29 fresh lung cancer specimens. Staining patterns were categorized to six groups based on the extent of positive staining and the localization of stained portions. While overexpression of CADM1 was observed on the cell surface of adenocarcinomas at a high frequency, around 60%, positive stainings were rarely observed on that of other lung carcinomas including squamous cell carcinomas. 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Natl. Acad. Sci. USA 105, 7287-7292, 2008). Twenty-one distinct Ags highly expressed on several carcinomas were identified and 356 mAbs with unique sequences turned out to bind to one of the 21 Ags. Among them CADM1/IGSF4 which had been originally referred to as tumor suppressor lung cancer 1 (TSLC1) was included. Therefore we examined the expression of CADM1 in lung cancers in this study. Eight different anti CADM1 mAbs were used for immunohistochemical analysis of 29 fresh lung cancer specimens. Staining patterns were categorized to six groups based on the extent of positive staining and the localization of stained portions. While overexpression of CADM1 was observed on the cell surface of adenocarcinomas at a high frequency, around 60%, positive stainings were rarely observed on that of other lung carcinomas including squamous cell carcinomas. Moreover, some clones among the eight mAbs gave different staining patterns from those by the other clones against the same fresh specimen, suggesting presence of variant forms of CADM1 differentiated by mAbs.</description><subject>Adenocarcinoma - immunology</subject><subject>Amino Acid Sequence</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antigens, Neoplasm - biosynthesis</subject><subject>Antigens, Neoplasm - immunology</subject><subject>Cell Adhesion Molecule-1</subject><subject>Cell Adhesion Molecules</subject><subject>Epitopes - immunology</subject><subject>Human monoclonal antibodies</subject><subject>Humans</subject><subject>Immunoglobulins - biosynthesis</subject><subject>Immunoglobulins - immunology</subject><subject>Immunohistochemical analysis</subject><subject>Lung Neoplasms - immunology</subject><subject>Membrane Proteins - biosynthesis</subject><subject>Membrane Proteins - immunology</subject><subject>Tumor suppressor</subject><subject>Tumor Suppressor Proteins - biosynthesis</subject><subject>Tumor Suppressor Proteins - immunology</subject><subject>Tumor-associated antigens</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkM1KAzEURoMotv68gAuZlbsZ700y7QR0UaqtguJCBXchydyRlHZSk1b07Z3SgjtdZXO-w81h7AyhQMDB5aywNrqCA6gCZAFC7bE-goKcI8h91geAQc4VvvXYUUozAEQ5UIesh0oMccixz64nkT7W1K6y8EmRvpaRUvKhzUKTjUc3j3h5P32eyMy32XzdvmempjY4E51vw8KcsIPGzBOd7t5j9jq5fRnf5Q9P0_vx6CF3oipXeVUToFRYoyBXldZK5xAqKE1ZSds0wpi6sZVFIbhSpbTdj8rSOu6wqU23OmYXW-8yhu7atNILnxzN56alsE56MORccc7_BTmUQyHFxsi3oIshpUiNXka_MPFbI-hNXT3Tm7p6U1eD1F3dbnS-s6_tgurfyS5nB1xtAepifHqKOjlPraPaR3IrXQf_l_8H4sGJ3g</recordid><startdate>20090612</startdate><enddate>20090612</enddate><creator>Kitamura, Yuka</creator><creator>Kurosawa, Gene</creator><creator>Tanaka, Miho</creator><creator>Sumitomo, Mariko</creator><creator>Muramatsu, Chiho</creator><creator>Eguchi, Keiko</creator><creator>Akahori, Yasushi</creator><creator>Iba, Yoshitaka</creator><creator>Tsuda, Hiroyuki</creator><creator>Sugiura, Mototaka</creator><creator>Hattori, Yoshinobu</creator><creator>Kurosawa, Yoshikazu</creator><general>Elsevier Inc</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20090612</creationdate><title>Frequent overexpression of CADM1/IGSF4 in lung adenocarcinoma</title><author>Kitamura, Yuka ; Kurosawa, Gene ; Tanaka, Miho ; Sumitomo, Mariko ; Muramatsu, Chiho ; Eguchi, Keiko ; Akahori, Yasushi ; Iba, Yoshitaka ; Tsuda, Hiroyuki ; Sugiura, Mototaka ; Hattori, Yoshinobu ; Kurosawa, Yoshikazu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-8de01491d13ec85bb4cc10805a584bff3aadfb8b13329954b00955bc2c1fdad13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adenocarcinoma - immunology</topic><topic>Amino Acid Sequence</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antigens, Neoplasm - biosynthesis</topic><topic>Antigens, Neoplasm - immunology</topic><topic>Cell Adhesion Molecule-1</topic><topic>Cell Adhesion Molecules</topic><topic>Epitopes - immunology</topic><topic>Human monoclonal antibodies</topic><topic>Humans</topic><topic>Immunoglobulins - biosynthesis</topic><topic>Immunoglobulins - immunology</topic><topic>Immunohistochemical analysis</topic><topic>Lung Neoplasms - immunology</topic><topic>Membrane Proteins - biosynthesis</topic><topic>Membrane Proteins - immunology</topic><topic>Tumor suppressor</topic><topic>Tumor Suppressor Proteins - biosynthesis</topic><topic>Tumor Suppressor Proteins - immunology</topic><topic>Tumor-associated antigens</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kitamura, Yuka</creatorcontrib><creatorcontrib>Kurosawa, Gene</creatorcontrib><creatorcontrib>Tanaka, Miho</creatorcontrib><creatorcontrib>Sumitomo, Mariko</creatorcontrib><creatorcontrib>Muramatsu, Chiho</creatorcontrib><creatorcontrib>Eguchi, Keiko</creatorcontrib><creatorcontrib>Akahori, Yasushi</creatorcontrib><creatorcontrib>Iba, Yoshitaka</creatorcontrib><creatorcontrib>Tsuda, Hiroyuki</creatorcontrib><creatorcontrib>Sugiura, Mototaka</creatorcontrib><creatorcontrib>Hattori, Yoshinobu</creatorcontrib><creatorcontrib>Kurosawa, Yoshikazu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kitamura, Yuka</au><au>Kurosawa, Gene</au><au>Tanaka, Miho</au><au>Sumitomo, Mariko</au><au>Muramatsu, Chiho</au><au>Eguchi, Keiko</au><au>Akahori, Yasushi</au><au>Iba, Yoshitaka</au><au>Tsuda, Hiroyuki</au><au>Sugiura, Mototaka</au><au>Hattori, Yoshinobu</au><au>Kurosawa, Yoshikazu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Frequent overexpression of CADM1/IGSF4 in lung adenocarcinoma</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2009-06-12</date><risdate>2009</risdate><volume>383</volume><issue>4</issue><spage>480</spage><epage>484</epage><pages>480-484</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>We reported comprehensive screening for antigens (Ags) overexpressed on various carcinomas via isolation of human monoclonal antibodies (mAbs) that may be therapeutic in a previous paper (Proc. Natl. Acad. Sci. USA 105, 7287-7292, 2008). Twenty-one distinct Ags highly expressed on several carcinomas were identified and 356 mAbs with unique sequences turned out to bind to one of the 21 Ags. Among them CADM1/IGSF4 which had been originally referred to as tumor suppressor lung cancer 1 (TSLC1) was included. Therefore we examined the expression of CADM1 in lung cancers in this study. Eight different anti CADM1 mAbs were used for immunohistochemical analysis of 29 fresh lung cancer specimens. Staining patterns were categorized to six groups based on the extent of positive staining and the localization of stained portions. While overexpression of CADM1 was observed on the cell surface of adenocarcinomas at a high frequency, around 60%, positive stainings were rarely observed on that of other lung carcinomas including squamous cell carcinomas. 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subjects | Adenocarcinoma - immunology Amino Acid Sequence Antibodies, Monoclonal - immunology Antigens, Neoplasm - biosynthesis Antigens, Neoplasm - immunology Cell Adhesion Molecule-1 Cell Adhesion Molecules Epitopes - immunology Human monoclonal antibodies Humans Immunoglobulins - biosynthesis Immunoglobulins - immunology Immunohistochemical analysis Lung Neoplasms - immunology Membrane Proteins - biosynthesis Membrane Proteins - immunology Tumor suppressor Tumor Suppressor Proteins - biosynthesis Tumor Suppressor Proteins - immunology Tumor-associated antigens |
title | Frequent overexpression of CADM1/IGSF4 in lung adenocarcinoma |
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