Removal of Sialic Acid from the Surface of Human MCF-7 Mammary Cancer Cells Abolishes E-Cadherin-Dependent Cell-Cell Adhesion in an Aggregation Assay
MCF-7 human breast cancer cells express E-cadherin and show, at least in some circumstances, E-cadherin-dependent cell-cell adhesion (Bracke et al., 1993).The MCF-7/AZ variant spontaneously displays E-cadherin-dependent fast aggregation; in the MCF-7/6 variant, E-cadherin appeared not to be spontane...
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Veröffentlicht in: | In vitro cellular & developmental biology. Animal 1995-09, Vol.31 (8), p.633-639 |
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creator | Deman, J J Van Larebeke, N A Bruyneel, E A Bracke, M E Vermeulen, S J Vennekens, K M Mareel, M M |
description | MCF-7 human breast cancer cells express E-cadherin and show, at least in some circumstances, E-cadherin-dependent cell-cell adhesion (Bracke et al., 1993).The MCF-7/AZ variant spontaneously displays E-cadherin-dependent fast aggregation; in the MCF-7/6 variant, E-cadherin appeared not to be spontaneously functional in the conditions of the fast aggregation assay, but function could be induced by incubation of the suspended cells in the presence of insulinlike growth factor I (IGF-I) (Bracke et al, 1993). E-cadherin from MCF-7 cells was shown to contain sialic acid. Treatment with neuraminidase was shown to remove this sialic acid, as well as most of the sialic acid present at the cell surface. Applied to MCF-7/AZ, and MCF-7/6 cells, pretreatment with neuraminidase abolished spontaneous as well as IGF-I induced, E-cadherin-dependent fast cell-cell adhesion of cells in suspension, as measured in the fast aggregation assay. Treatment with neuraminidase did not, however, inhibit the possibly different, but equally E-cadherin-mediated, process of cell-cell adhesion of MCF-7 cells on a flat plastic substrate as assessed by determining the percentage of cells remaining isolated (without contact with other cells) 24 h after plating. |
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E-cadherin from MCF-7 cells was shown to contain sialic acid. Treatment with neuraminidase was shown to remove this sialic acid, as well as most of the sialic acid present at the cell surface. Applied to MCF-7/AZ, and MCF-7/6 cells, pretreatment with neuraminidase abolished spontaneous as well as IGF-I induced, E-cadherin-dependent fast cell-cell adhesion of cells in suspension, as measured in the fast aggregation assay. Treatment with neuraminidase did not, however, inhibit the possibly different, but equally E-cadherin-mediated, process of cell-cell adhesion of MCF-7 cells on a flat plastic substrate as assessed by determining the percentage of cells remaining isolated (without contact with other cells) 24 h after plating.</description><identifier>ISSN: 1071-2690</identifier><identifier>EISSN: 1543-706X</identifier><identifier>DOI: 10.1007/BF02634317</identifier><identifier>PMID: 8528519</identifier><language>eng</language><publisher>Germany: Society for In Vitro Biology</publisher><subject>Adhesive bonding ; Adhesives ; Aggregation ; Antibodies ; Breast Neoplasms ; Cadherins ; Cadherins - metabolism ; Calcium ; Cell Adhesion ; Cell Aggregation ; Cell Membrane - metabolism ; Cultured cells ; Female ; Growth, Differentiation and Senescence ; Humans ; Molecules ; N-Acetylneuraminic Acid ; Neurons ; Sialic Acids - metabolism ; Tumor Cells, Cultured</subject><ispartof>In vitro cellular & developmental biology. 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Animal</title><addtitle>In Vitro Cell Dev Biol Anim</addtitle><description>MCF-7 human breast cancer cells express E-cadherin and show, at least in some circumstances, E-cadherin-dependent cell-cell adhesion (Bracke et al., 1993).The MCF-7/AZ variant spontaneously displays E-cadherin-dependent fast aggregation; in the MCF-7/6 variant, E-cadherin appeared not to be spontaneously functional in the conditions of the fast aggregation assay, but function could be induced by incubation of the suspended cells in the presence of insulinlike growth factor I (IGF-I) (Bracke et al, 1993). E-cadherin from MCF-7 cells was shown to contain sialic acid. Treatment with neuraminidase was shown to remove this sialic acid, as well as most of the sialic acid present at the cell surface. Applied to MCF-7/AZ, and MCF-7/6 cells, pretreatment with neuraminidase abolished spontaneous as well as IGF-I induced, E-cadherin-dependent fast cell-cell adhesion of cells in suspension, as measured in the fast aggregation assay. Treatment with neuraminidase did not, however, inhibit the possibly different, but equally E-cadherin-mediated, process of cell-cell adhesion of MCF-7 cells on a flat plastic substrate as assessed by determining the percentage of cells remaining isolated (without contact with other cells) 24 h after plating.</description><subject>Adhesive bonding</subject><subject>Adhesives</subject><subject>Aggregation</subject><subject>Antibodies</subject><subject>Breast Neoplasms</subject><subject>Cadherins</subject><subject>Cadherins - metabolism</subject><subject>Calcium</subject><subject>Cell Adhesion</subject><subject>Cell Aggregation</subject><subject>Cell Membrane - metabolism</subject><subject>Cultured cells</subject><subject>Female</subject><subject>Growth, Differentiation and Senescence</subject><subject>Humans</subject><subject>Molecules</subject><subject>N-Acetylneuraminic Acid</subject><subject>Neurons</subject><subject>Sialic Acids - metabolism</subject><subject>Tumor Cells, Cultured</subject><issn>1071-2690</issn><issn>1543-706X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkU1v1DAQhi0EKqVw4QySTxyQDP5KvDmG0KVIrZAoSNyiSTzedZXEWztB6g_h_-Kwq-KDbfl59Go8Q8hrwT8Izs3HT1suS6WVME_IuSi0YoaXv57mOzeCybLiz8mLlO54XpUoz8jZppCbQlTn5M93HMNvGGhw9NbD4Hta995SF8NI5z3S2yU66HHlV8sIE71ptszQGxhHiA-0ganHSBschkTrLgw-7THRS9aA3WP0E_uMB5wsTvM_ia0brTNLPkzUTzRH1rtdxB3M60udEjy8JM8cDAlfnc4L8nN7-aO5Ytffvnxt6mvWK65mVjpeWNFJwx0oZzmCqyB_sURhQHeKd12hqo22XEkhtQV0FdeFLXpdyBK5uiDvjrmHGO4XTHM7-tTnCmHCsKTWmLISQsosvj-KfQwpRXTtIfq1Aa3g7TqD9v8Msvz2lLp0I9pH9dT0zN8c-V2aQ3zEWlZab4T6CwDHiZc</recordid><startdate>19950901</startdate><enddate>19950901</enddate><creator>Deman, J J</creator><creator>Van Larebeke, N A</creator><creator>Bruyneel, E A</creator><creator>Bracke, M E</creator><creator>Vermeulen, S J</creator><creator>Vennekens, K M</creator><creator>Mareel, M M</creator><general>Society for In Vitro Biology</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>19950901</creationdate><title>Removal of Sialic Acid from the Surface of Human MCF-7 Mammary Cancer Cells Abolishes E-Cadherin-Dependent Cell-Cell Adhesion in an Aggregation Assay</title><author>Deman, J J ; Van Larebeke, N A ; Bruyneel, E A ; Bracke, M E ; Vermeulen, S J ; Vennekens, K M ; Mareel, M M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c303t-6f05d1b270fa3fd0eaf9a0096e17a4b30bb53984d032124daef9045d5c4526e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adhesive bonding</topic><topic>Adhesives</topic><topic>Aggregation</topic><topic>Antibodies</topic><topic>Breast Neoplasms</topic><topic>Cadherins</topic><topic>Cadherins - metabolism</topic><topic>Calcium</topic><topic>Cell Adhesion</topic><topic>Cell Aggregation</topic><topic>Cell Membrane - metabolism</topic><topic>Cultured cells</topic><topic>Female</topic><topic>Growth, Differentiation and Senescence</topic><topic>Humans</topic><topic>Molecules</topic><topic>N-Acetylneuraminic Acid</topic><topic>Neurons</topic><topic>Sialic Acids - metabolism</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deman, J J</creatorcontrib><creatorcontrib>Van Larebeke, N A</creatorcontrib><creatorcontrib>Bruyneel, E A</creatorcontrib><creatorcontrib>Bracke, M E</creatorcontrib><creatorcontrib>Vermeulen, S J</creatorcontrib><creatorcontrib>Vennekens, K M</creatorcontrib><creatorcontrib>Mareel, M M</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>In vitro cellular & developmental biology. Animal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deman, J J</au><au>Van Larebeke, N A</au><au>Bruyneel, E A</au><au>Bracke, M E</au><au>Vermeulen, S J</au><au>Vennekens, K M</au><au>Mareel, M M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Removal of Sialic Acid from the Surface of Human MCF-7 Mammary Cancer Cells Abolishes E-Cadherin-Dependent Cell-Cell Adhesion in an Aggregation Assay</atitle><jtitle>In vitro cellular & developmental biology. Animal</jtitle><addtitle>In Vitro Cell Dev Biol Anim</addtitle><date>1995-09-01</date><risdate>1995</risdate><volume>31</volume><issue>8</issue><spage>633</spage><epage>639</epage><pages>633-639</pages><issn>1071-2690</issn><eissn>1543-706X</eissn><abstract>MCF-7 human breast cancer cells express E-cadherin and show, at least in some circumstances, E-cadherin-dependent cell-cell adhesion (Bracke et al., 1993).The MCF-7/AZ variant spontaneously displays E-cadherin-dependent fast aggregation; in the MCF-7/6 variant, E-cadherin appeared not to be spontaneously functional in the conditions of the fast aggregation assay, but function could be induced by incubation of the suspended cells in the presence of insulinlike growth factor I (IGF-I) (Bracke et al, 1993). E-cadherin from MCF-7 cells was shown to contain sialic acid. Treatment with neuraminidase was shown to remove this sialic acid, as well as most of the sialic acid present at the cell surface. Applied to MCF-7/AZ, and MCF-7/6 cells, pretreatment with neuraminidase abolished spontaneous as well as IGF-I induced, E-cadherin-dependent fast cell-cell adhesion of cells in suspension, as measured in the fast aggregation assay. Treatment with neuraminidase did not, however, inhibit the possibly different, but equally E-cadherin-mediated, process of cell-cell adhesion of MCF-7 cells on a flat plastic substrate as assessed by determining the percentage of cells remaining isolated (without contact with other cells) 24 h after plating.</abstract><cop>Germany</cop><pub>Society for In Vitro Biology</pub><pmid>8528519</pmid><doi>10.1007/BF02634317</doi><tpages>7</tpages></addata></record> |
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subjects | Adhesive bonding Adhesives Aggregation Antibodies Breast Neoplasms Cadherins Cadherins - metabolism Calcium Cell Adhesion Cell Aggregation Cell Membrane - metabolism Cultured cells Female Growth, Differentiation and Senescence Humans Molecules N-Acetylneuraminic Acid Neurons Sialic Acids - metabolism Tumor Cells, Cultured |
title | Removal of Sialic Acid from the Surface of Human MCF-7 Mammary Cancer Cells Abolishes E-Cadherin-Dependent Cell-Cell Adhesion in an Aggregation Assay |
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