Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Biochemical and biophysical research communications 2009-06, Vol.383 (4), p.480-484
Main Authors: Kitamura, Yuka, Kurosawa, Gene, Tanaka, Miho, Sumitomo, Mariko, Muramatsu, Chiho, Eguchi, Keiko, Akahori, Yasushi, Iba, Yoshitaka, Tsuda, Hiroyuki, Sugiura, Mototaka, Hattori, Yoshinobu, Kurosawa, Yoshikazu
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c385t-8de01491d13ec85bb4cc10805a584bff3aadfb8b13329954b00955bc2c1fdad13
cites cdi_FETCH-LOGICAL-c385t-8de01491d13ec85bb4cc10805a584bff3aadfb8b13329954b00955bc2c1fdad13
container_end_page 484
container_issue 4
container_start_page 480
container_title Biochemical and biophysical research communications
container_volume 383
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67229222</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006291X09007281</els_id><sourcerecordid>20573431</sourcerecordid><originalsourceid>FETCH-LOGICAL-c385t-8de01491d13ec85bb4cc10805a584bff3aadfb8b13329954b00955bc2c1fdad13</originalsourceid><addsrcrecordid>eNqFkM1KAzEURoMotv68gAuZlbsZ700y7QR0UaqtguJCBXchydyRlHZSk1b07Z3SgjtdZXO-w81h7AyhQMDB5aywNrqCA6gCZAFC7bE-goKcI8h91geAQc4VvvXYUUozAEQ5UIesh0oMccixz64nkT7W1K6y8EmRvpaRUvKhzUKTjUc3j3h5P32eyMy32XzdvmempjY4E51vw8KcsIPGzBOd7t5j9jq5fRnf5Q9P0_vx6CF3oipXeVUToFRYoyBXldZK5xAqKE1ZSds0wpi6sZVFIbhSpbTdj8rSOu6wqU23OmYXW-8yhu7atNILnxzN56alsE56MORccc7_BTmUQyHFxsi3oIshpUiNXka_MPFbI-hNXT3Tm7p6U1eD1F3dbnS-s6_tgurfyS5nB1xtAepifHqKOjlPraPaR3IrXQf_l_8H4sGJ3g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20573431</pqid></control><display><type>article</type><title>Frequent overexpression of CADM1/IGSF4 in lung adenocarcinoma</title><source>Elsevier</source><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</creator><creatorcontrib>Kitamura, Yuka ; Kurosawa, Gene ; Tanaka, Miho ; Sumitomo, Mariko ; Muramatsu, Chiho ; Eguchi, Keiko ; Akahori, Yasushi ; Iba, Yoshitaka ; Tsuda, Hiroyuki ; Sugiura, Mototaka ; Hattori, Yoshinobu ; Kurosawa, Yoshikazu</creatorcontrib><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.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2009.04.039</identifier><identifier>PMID: 19371721</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>Biochemical and biophysical research communications, 2009-06, Vol.383 (4), p.480-484</ispartof><rights>2009 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-8de01491d13ec85bb4cc10805a584bff3aadfb8b13329954b00955bc2c1fdad13</citedby><cites>FETCH-LOGICAL-c385t-8de01491d13ec85bb4cc10805a584bff3aadfb8b13329954b00955bc2c1fdad13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19371721$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Frequent overexpression of CADM1/IGSF4 in lung adenocarcinoma</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><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.</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. 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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19371721</pmid><doi>10.1016/j.bbrc.2009.04.039</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0006-291X
ispartof Biochemical and biophysical research communications, 2009-06, Vol.383 (4), p.480-484
issn 0006-291X
1090-2104
language eng
recordid cdi_proquest_miscellaneous_67229222
source Elsevier
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T16%3A59%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Frequent%20overexpression%20of%20CADM1/IGSF4%20in%20lung%20adenocarcinoma&rft.jtitle=Biochemical%20and%20biophysical%20research%20communications&rft.au=Kitamura,%20Yuka&rft.date=2009-06-12&rft.volume=383&rft.issue=4&rft.spage=480&rft.epage=484&rft.pages=480-484&rft.issn=0006-291X&rft.eissn=1090-2104&rft_id=info:doi/10.1016/j.bbrc.2009.04.039&rft_dat=%3Cproquest_cross%3E20573431%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c385t-8de01491d13ec85bb4cc10805a584bff3aadfb8b13329954b00955bc2c1fdad13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=20573431&rft_id=info:pmid/19371721&rfr_iscdi=true