CD44-Associated Tn Antigen as a New Biomarker of Tumor Cells with Aberrant Glycosylation
Tn antigen is a tumor-associated antigen that appears on cancer cells as a result of aberrant O-glycosylation. The most studied form of Tn antigen is found in mucins, in particular, in mucin 1 (MUC1). Antibodies against this form of Tn antigen are used to diagnose tumors, as well as to generate T-ki...
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Veröffentlicht in: | Biochemistry (Moscow) 2020-09, Vol.85 (9), p.1064-1071 |
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description | Tn antigen is a tumor-associated antigen that appears on cancer cells as a result of aberrant O-glycosylation. The most studied form of Tn antigen is found in mucins, in particular, in mucin 1 (MUC1). Antibodies against this form of Tn antigen are used to diagnose tumors, as well as to generate T-killers with a chimeric receptor. Some carcinomas do not carry MUC1 and antibodies of a different specificity are required to detect Tn antigen on these cells. In our work, we searched for anti-Tn antibodies without preliminary assumptions about the proteins that may be carriers of the Tn antigen. For this purpose, we obtained several pairs of isogenic cell lines with the wild type and knockout of the
Cosmc
gene, which is essential for correct protein O-glycosylation. Using the created lines as immunogens, we generated a monoclonal antibody AKC3, which reacted with the Cosmc-deficient A549 lung adenocarcinoma cells and did not bind to the wild-type cells. Using mass spectrometry, as well as co-immunoprecipitation, it was shown that the AKC3 antibody recognized the Tn antigen in the context of CD44 protein – a protein important for tumor growth. The AKC3 antibody can be used for tumor diagnosis, and to generate T cells with a chimeric receptor for treatment of tumors that do not express mucins. |
doi_str_mv | 10.1134/S0006297920090060 |
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Cosmc
gene, which is essential for correct protein O-glycosylation. Using the created lines as immunogens, we generated a monoclonal antibody AKC3, which reacted with the Cosmc-deficient A549 lung adenocarcinoma cells and did not bind to the wild-type cells. Using mass spectrometry, as well as co-immunoprecipitation, it was shown that the AKC3 antibody recognized the Tn antigen in the context of CD44 protein – a protein important for tumor growth. The AKC3 antibody can be used for tumor diagnosis, and to generate T cells with a chimeric receptor for treatment of tumors that do not express mucins.</description><identifier>ISSN: 0006-2979</identifier><identifier>EISSN: 1608-3040</identifier><identifier>DOI: 10.1134/S0006297920090060</identifier><identifier>PMID: 33050853</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>A549 Cells ; Adenocarcinoma of Lung - diagnosis ; Adenocarcinoma of Lung - immunology ; Adenocarcinoma of Lung - metabolism ; Antibodies, Monoclonal - immunology ; Antigens ; Antigens, Tumor-Associated, Carbohydrate - immunology ; Antigens, Tumor-Associated, Carbohydrate - metabolism ; Biochemistry ; Biomarkers, Tumor - metabolism ; Biomedical and Life Sciences ; Biomedicine ; Bioorganic Chemistry ; CRISPR-Cas Systems ; Ethylenediaminetetraacetic acid ; Glycosylation ; Humans ; Hyaluronan Receptors - immunology ; Hyaluronan Receptors - metabolism ; Life Sciences ; Lung Neoplasms - diagnosis ; Lung Neoplasms - immunology ; Lung Neoplasms - metabolism ; Mass spectrometry ; Microbiology ; Molecular Chaperones - antagonists & inhibitors ; Molecular Chaperones - genetics ; Molecular Chaperones - metabolism ; Monoclonal antibodies ; Mucins ; T cells ; Tumors</subject><ispartof>Biochemistry (Moscow), 2020-09, Vol.85 (9), p.1064-1071</ispartof><rights>Pleiades Publishing, Ltd. 2020</rights><rights>COPYRIGHT 2020 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-7b655c1d1675f6cde5347a5dfb55e75c557286c52a085d4937528f4da9eaf34d3</citedby><cites>FETCH-LOGICAL-c411t-7b655c1d1675f6cde5347a5dfb55e75c557286c52a085d4937528f4da9eaf34d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0006297920090060$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0006297920090060$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33050853$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shuvalova, M. L.</creatorcontrib><creatorcontrib>Kopylov, A. T.</creatorcontrib><creatorcontrib>Mazurov, D. V.</creatorcontrib><creatorcontrib>Pichugin, A. V.</creatorcontrib><creatorcontrib>Bovin, N. V.</creatorcontrib><creatorcontrib>Filatov, A. V.</creatorcontrib><title>CD44-Associated Tn Antigen as a New Biomarker of Tumor Cells with Aberrant Glycosylation</title><title>Biochemistry (Moscow)</title><addtitle>Biochemistry Moscow</addtitle><addtitle>Biochemistry (Mosc)</addtitle><description>Tn antigen is a tumor-associated antigen that appears on cancer cells as a result of aberrant O-glycosylation. The most studied form of Tn antigen is found in mucins, in particular, in mucin 1 (MUC1). Antibodies against this form of Tn antigen are used to diagnose tumors, as well as to generate T-killers with a chimeric receptor. Some carcinomas do not carry MUC1 and antibodies of a different specificity are required to detect Tn antigen on these cells. In our work, we searched for anti-Tn antibodies without preliminary assumptions about the proteins that may be carriers of the Tn antigen. For this purpose, we obtained several pairs of isogenic cell lines with the wild type and knockout of the
Cosmc
gene, which is essential for correct protein O-glycosylation. Using the created lines as immunogens, we generated a monoclonal antibody AKC3, which reacted with the Cosmc-deficient A549 lung adenocarcinoma cells and did not bind to the wild-type cells. Using mass spectrometry, as well as co-immunoprecipitation, it was shown that the AKC3 antibody recognized the Tn antigen in the context of CD44 protein – a protein important for tumor growth. The AKC3 antibody can be used for tumor diagnosis, and to generate T cells with a chimeric receptor for treatment of tumors that do not express mucins.</description><subject>A549 Cells</subject><subject>Adenocarcinoma of Lung - diagnosis</subject><subject>Adenocarcinoma of Lung - immunology</subject><subject>Adenocarcinoma of Lung - metabolism</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antigens</subject><subject>Antigens, Tumor-Associated, Carbohydrate - immunology</subject><subject>Antigens, Tumor-Associated, Carbohydrate - metabolism</subject><subject>Biochemistry</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bioorganic Chemistry</subject><subject>CRISPR-Cas Systems</subject><subject>Ethylenediaminetetraacetic acid</subject><subject>Glycosylation</subject><subject>Humans</subject><subject>Hyaluronan Receptors - immunology</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Life Sciences</subject><subject>Lung Neoplasms - diagnosis</subject><subject>Lung Neoplasms - immunology</subject><subject>Lung Neoplasms - metabolism</subject><subject>Mass spectrometry</subject><subject>Microbiology</subject><subject>Molecular Chaperones - antagonists & inhibitors</subject><subject>Molecular Chaperones - genetics</subject><subject>Molecular Chaperones - metabolism</subject><subject>Monoclonal antibodies</subject><subject>Mucins</subject><subject>T cells</subject><subject>Tumors</subject><issn>0006-2979</issn><issn>1608-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kV9rFDEUxYModq1-AF8k4IsvU_N_Zh7HrVahtA-u4FvIJjdr6kxSkxnKfnuzbBWkRfKQ3JzfuVzuQeg1JWeUcvH-KyFEsb7tGSF9fZInaEUV6RpOBHmKVge5Oegn6EUpN7VkpOfP0QnnRJJO8hX6vj4XohlKSTaYGRzeRDzEOewgYlOwwVdwhz-ENJn8EzJOHm-WKWW8hnEs-C7MP_CwhZxNnPHFuLep7EczhxRfomfejAVe3d-n6Nunj5v15-by-uLLerhsrKB0btqtktJSR1UrvbIOJBetkc5vpYRWWilb1ikrmanzOtHzVrLOC2d6MJ4Lx0_Ru2Pf25x-LVBmPYVi63QmQlqKZkLWXdGWdhV9e0R3ZgQdok9zNvaA60FxxVQvGa_U2SNUPQ6mYFMEH-r_PwZ6NNicSsng9W0OdV97TYk-5KQf5FQ9b-6nXrYTuL-OP8FUgB2BUqW4g6xv0pJj3eR_uv4GOVCY8A</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Shuvalova, M. L.</creator><creator>Kopylov, A. T.</creator><creator>Mazurov, D. V.</creator><creator>Pichugin, A. V.</creator><creator>Bovin, N. V.</creator><creator>Filatov, A. V.</creator><general>Pleiades Publishing</general><general>Springer</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>7X8</scope></search><sort><creationdate>20200901</creationdate><title>CD44-Associated Tn Antigen as a New Biomarker of Tumor Cells with Aberrant Glycosylation</title><author>Shuvalova, M. L. ; Kopylov, A. T. ; Mazurov, D. V. ; Pichugin, A. V. ; Bovin, N. V. ; Filatov, A. V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-7b655c1d1675f6cde5347a5dfb55e75c557286c52a085d4937528f4da9eaf34d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>A549 Cells</topic><topic>Adenocarcinoma of Lung - diagnosis</topic><topic>Adenocarcinoma of Lung - immunology</topic><topic>Adenocarcinoma of Lung - metabolism</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antigens</topic><topic>Antigens, Tumor-Associated, Carbohydrate - immunology</topic><topic>Antigens, Tumor-Associated, Carbohydrate - metabolism</topic><topic>Biochemistry</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Bioorganic Chemistry</topic><topic>CRISPR-Cas Systems</topic><topic>Ethylenediaminetetraacetic acid</topic><topic>Glycosylation</topic><topic>Humans</topic><topic>Hyaluronan Receptors - immunology</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Life Sciences</topic><topic>Lung Neoplasms - diagnosis</topic><topic>Lung Neoplasms - immunology</topic><topic>Lung Neoplasms - metabolism</topic><topic>Mass spectrometry</topic><topic>Microbiology</topic><topic>Molecular Chaperones - antagonists & inhibitors</topic><topic>Molecular Chaperones - genetics</topic><topic>Molecular Chaperones - metabolism</topic><topic>Monoclonal antibodies</topic><topic>Mucins</topic><topic>T cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shuvalova, M. L.</creatorcontrib><creatorcontrib>Kopylov, A. T.</creatorcontrib><creatorcontrib>Mazurov, D. V.</creatorcontrib><creatorcontrib>Pichugin, A. V.</creatorcontrib><creatorcontrib>Bovin, N. V.</creatorcontrib><creatorcontrib>Filatov, A. V.</creatorcontrib><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>Biochemistry (Moscow)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shuvalova, M. L.</au><au>Kopylov, A. T.</au><au>Mazurov, D. V.</au><au>Pichugin, A. V.</au><au>Bovin, N. V.</au><au>Filatov, A. V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD44-Associated Tn Antigen as a New Biomarker of Tumor Cells with Aberrant Glycosylation</atitle><jtitle>Biochemistry (Moscow)</jtitle><stitle>Biochemistry Moscow</stitle><addtitle>Biochemistry (Mosc)</addtitle><date>2020-09-01</date><risdate>2020</risdate><volume>85</volume><issue>9</issue><spage>1064</spage><epage>1071</epage><pages>1064-1071</pages><issn>0006-2979</issn><eissn>1608-3040</eissn><abstract>Tn antigen is a tumor-associated antigen that appears on cancer cells as a result of aberrant O-glycosylation. The most studied form of Tn antigen is found in mucins, in particular, in mucin 1 (MUC1). Antibodies against this form of Tn antigen are used to diagnose tumors, as well as to generate T-killers with a chimeric receptor. Some carcinomas do not carry MUC1 and antibodies of a different specificity are required to detect Tn antigen on these cells. In our work, we searched for anti-Tn antibodies without preliminary assumptions about the proteins that may be carriers of the Tn antigen. For this purpose, we obtained several pairs of isogenic cell lines with the wild type and knockout of the
Cosmc
gene, which is essential for correct protein O-glycosylation. Using the created lines as immunogens, we generated a monoclonal antibody AKC3, which reacted with the Cosmc-deficient A549 lung adenocarcinoma cells and did not bind to the wild-type cells. Using mass spectrometry, as well as co-immunoprecipitation, it was shown that the AKC3 antibody recognized the Tn antigen in the context of CD44 protein – a protein important for tumor growth. The AKC3 antibody can be used for tumor diagnosis, and to generate T cells with a chimeric receptor for treatment of tumors that do not express mucins.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><pmid>33050853</pmid><doi>10.1134/S0006297920090060</doi><tpages>8</tpages></addata></record> |
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subjects | A549 Cells Adenocarcinoma of Lung - diagnosis Adenocarcinoma of Lung - immunology Adenocarcinoma of Lung - metabolism Antibodies, Monoclonal - immunology Antigens Antigens, Tumor-Associated, Carbohydrate - immunology Antigens, Tumor-Associated, Carbohydrate - metabolism Biochemistry Biomarkers, Tumor - metabolism Biomedical and Life Sciences Biomedicine Bioorganic Chemistry CRISPR-Cas Systems Ethylenediaminetetraacetic acid Glycosylation Humans Hyaluronan Receptors - immunology Hyaluronan Receptors - metabolism Life Sciences Lung Neoplasms - diagnosis Lung Neoplasms - immunology Lung Neoplasms - metabolism Mass spectrometry Microbiology Molecular Chaperones - antagonists & inhibitors Molecular Chaperones - genetics Molecular Chaperones - metabolism Monoclonal antibodies Mucins T cells Tumors |
title | CD44-Associated Tn Antigen as a New Biomarker of Tumor Cells with Aberrant Glycosylation |
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