Differential expression of α-2,3-sialyltransferases and α-1,3/4-fucosyltransferases regulates the levels of sialyl Lewis a and sialyl Lewis x in gastrointestinal carcinoma cells

Sialyl Lewis x and sialyl Lewis a expression depends on sialyltransferases and fucosyltransferases. In this study, we screened for major variations of sialyltransferases and fucosyltransferases involved in the synthesis and regulation of sialyl Lewis x and sialyl Lewis a epitopes in gastrointestinal...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The international journal of biochemistry & cell biology 2010-01, Vol.42 (1), p.80-89
Hauptverfasser: Carvalho, A.S., Harduin-Lepers, A., Magalhães, A., Machado, E., Mendes, N., Costa, L.T., Matthiesen, R., Almeida, R., Costa, J., Reis, C.A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 89
container_issue 1
container_start_page 80
container_title The international journal of biochemistry & cell biology
container_volume 42
creator Carvalho, A.S.
Harduin-Lepers, A.
Magalhães, A.
Machado, E.
Mendes, N.
Costa, L.T.
Matthiesen, R.
Almeida, R.
Costa, J.
Reis, C.A.
description Sialyl Lewis x and sialyl Lewis a expression depends on sialyltransferases and fucosyltransferases. In this study, we screened for major variations of sialyltransferases and fucosyltransferases involved in the synthesis and regulation of sialyl Lewis x and sialyl Lewis a epitopes in gastrointestinal carcinoma cells. Our results show that expression of ST3Gal IV in several gastrointestinal cell lines is correlated with the expression of sialyl Lewis x at the cell surface. ST3Gal IV overexpressed in the gastric MKN45 cell line, showed exclusive enzymatic activity towards glycoproteins containing terminal Galβ1-4GlcNAc structure. On the other hand, when ST3Gal III was overexpressed in MKN45, an increase in the expression levels of both sialyl Lewis epitopes was observed. ST3Gal III and ST3Gal IV lead to de novo synthesis of sialyl Lewis x determinant on different molecular weight glycoproteins of MKN45 cells suggesting that each enzyme used different substrates within the available glycoproteome. The final glycosylation step in sialyl Lewis x and sialyl Lewis a biosynthesis in MKN45 cell line was shown to be associated to FUT5, which efficiently fucosylated sialyl Lewis precursors on glycoproteins. Moreover we demonstrate that the expression of sialyl Lewis epitopes in the MKN45 was induced by cell confluence, which can be regarded as a model to study altered glycosylation during tumour progression. This increase was observed together with an increase in mRNA levels of ST3GAL3, FUT5 and FUT6, and a decrease in FUT4 transcript levels in MKN45 confluent cells, suggesting a possible control at the transcriptional level.
doi_str_mv 10.1016/j.biocel.2009.09.010
format Article
fullrecord <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00423661v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1357272509002660</els_id><sourcerecordid>734161803</sourcerecordid><originalsourceid>FETCH-LOGICAL-c395t-5c3d190e00c2965c8f21a56f594e54eaf6d2e938f78d5c3ccb0815f7f71e64ba3</originalsourceid><addsrcrecordid>eNp9kc2KFDEQx4Mo7rr6BiK5ibA9m-p0-uMiLOvHCgNe9Bwy6cpuhp5kTHWPu48lvofPZNoeFD0IBSmqfvWvShVjz0GsQEB9sV1tfLQ4rEohutVsIB6wU2ibtlBtox5mX6qmKJtSnbAnRFshBKhSPmYn0DUt1DWcsu9vvHOYMIzeDBzv9gmJfAw8Ov7jW1Gey4Jy5n4YkwmUSUNI3IR-zsK5vKgKN9lI_wAJb6bBjNkbb5EPeMCBZslFi6_xq88qv3T-Ct1xH_iNoTFFH3L56EMey5pkfYg7w_N_B3rKHjkzED47vmfs87u3n66ui_XH9x-uLteFlZ0aC2VlD51AIWzZ1cq2rgSjaqe6ClWFxtV9iZ1sXdP2mbV2I1pQrnENYF1tjDxjrxbdWzPoffI7k-51NF5fX671HBOiKmVe4wEy-3Jh9yl-mfLgeudpntYEjBPpRlZQQytkJquFtCkSJXS_pUHo-bJ6q5fL6vmyejYQuezFscG02WH_p-h4ygy8XoC8ajx4TJqsx2Cx9wntqPvo_9_hJ14muq0</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>734161803</pqid></control><display><type>article</type><title>Differential expression of α-2,3-sialyltransferases and α-1,3/4-fucosyltransferases regulates the levels of sialyl Lewis a and sialyl Lewis x in gastrointestinal carcinoma cells</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Carvalho, A.S. ; Harduin-Lepers, A. ; Magalhães, A. ; Machado, E. ; Mendes, N. ; Costa, L.T. ; Matthiesen, R. ; Almeida, R. ; Costa, J. ; Reis, C.A.</creator><creatorcontrib>Carvalho, A.S. ; Harduin-Lepers, A. ; Magalhães, A. ; Machado, E. ; Mendes, N. ; Costa, L.T. ; Matthiesen, R. ; Almeida, R. ; Costa, J. ; Reis, C.A.</creatorcontrib><description>Sialyl Lewis x and sialyl Lewis a expression depends on sialyltransferases and fucosyltransferases. In this study, we screened for major variations of sialyltransferases and fucosyltransferases involved in the synthesis and regulation of sialyl Lewis x and sialyl Lewis a epitopes in gastrointestinal carcinoma cells. Our results show that expression of ST3Gal IV in several gastrointestinal cell lines is correlated with the expression of sialyl Lewis x at the cell surface. ST3Gal IV overexpressed in the gastric MKN45 cell line, showed exclusive enzymatic activity towards glycoproteins containing terminal Galβ1-4GlcNAc structure. On the other hand, when ST3Gal III was overexpressed in MKN45, an increase in the expression levels of both sialyl Lewis epitopes was observed. ST3Gal III and ST3Gal IV lead to de novo synthesis of sialyl Lewis x determinant on different molecular weight glycoproteins of MKN45 cells suggesting that each enzyme used different substrates within the available glycoproteome. The final glycosylation step in sialyl Lewis x and sialyl Lewis a biosynthesis in MKN45 cell line was shown to be associated to FUT5, which efficiently fucosylated sialyl Lewis precursors on glycoproteins. Moreover we demonstrate that the expression of sialyl Lewis epitopes in the MKN45 was induced by cell confluence, which can be regarded as a model to study altered glycosylation during tumour progression. This increase was observed together with an increase in mRNA levels of ST3GAL3, FUT5 and FUT6, and a decrease in FUT4 transcript levels in MKN45 confluent cells, suggesting a possible control at the transcriptional level.</description><identifier>ISSN: 1357-2725</identifier><identifier>EISSN: 1878-5875</identifier><identifier>DOI: 10.1016/j.biocel.2009.09.010</identifier><identifier>PMID: 19781661</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Antigens, Tumor-Associated, Carbohydrate - metabolism ; Biochemistry, Molecular Biology ; Cell confluence ; Cell Count ; Cell Extracts ; Cell Line, Tumor ; Fucosyltransferases - genetics ; Fucosyltransferases - metabolism ; Gastric cancer ; Gene Expression Regulation, Enzymologic ; Gene Expression Regulation, Neoplastic ; Humans ; Life Sciences ; mRNA expression ; Oligosaccharides - metabolism ; Sialyl Lewis a and sialyl Lewis x ; Sialyltransferase ; Sialyltransferases - genetics ; Sialyltransferases - metabolism ; Stomach Neoplasms - enzymology ; Stomach Neoplasms - genetics ; Stomach Neoplasms - pathology ; Transfection</subject><ispartof>The international journal of biochemistry &amp; cell biology, 2010-01, Vol.42 (1), p.80-89</ispartof><rights>2009 Elsevier Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-5c3d190e00c2965c8f21a56f594e54eaf6d2e938f78d5c3ccb0815f7f71e64ba3</citedby><cites>FETCH-LOGICAL-c395t-5c3d190e00c2965c8f21a56f594e54eaf6d2e938f78d5c3ccb0815f7f71e64ba3</cites><orcidid>0000-0002-1233-3799 ; 0000-0003-2888-9617</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1357272509002660$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19781661$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00423661$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Carvalho, A.S.</creatorcontrib><creatorcontrib>Harduin-Lepers, A.</creatorcontrib><creatorcontrib>Magalhães, A.</creatorcontrib><creatorcontrib>Machado, E.</creatorcontrib><creatorcontrib>Mendes, N.</creatorcontrib><creatorcontrib>Costa, L.T.</creatorcontrib><creatorcontrib>Matthiesen, R.</creatorcontrib><creatorcontrib>Almeida, R.</creatorcontrib><creatorcontrib>Costa, J.</creatorcontrib><creatorcontrib>Reis, C.A.</creatorcontrib><title>Differential expression of α-2,3-sialyltransferases and α-1,3/4-fucosyltransferases regulates the levels of sialyl Lewis a and sialyl Lewis x in gastrointestinal carcinoma cells</title><title>The international journal of biochemistry &amp; cell biology</title><addtitle>Int J Biochem Cell Biol</addtitle><description>Sialyl Lewis x and sialyl Lewis a expression depends on sialyltransferases and fucosyltransferases. In this study, we screened for major variations of sialyltransferases and fucosyltransferases involved in the synthesis and regulation of sialyl Lewis x and sialyl Lewis a epitopes in gastrointestinal carcinoma cells. Our results show that expression of ST3Gal IV in several gastrointestinal cell lines is correlated with the expression of sialyl Lewis x at the cell surface. ST3Gal IV overexpressed in the gastric MKN45 cell line, showed exclusive enzymatic activity towards glycoproteins containing terminal Galβ1-4GlcNAc structure. On the other hand, when ST3Gal III was overexpressed in MKN45, an increase in the expression levels of both sialyl Lewis epitopes was observed. ST3Gal III and ST3Gal IV lead to de novo synthesis of sialyl Lewis x determinant on different molecular weight glycoproteins of MKN45 cells suggesting that each enzyme used different substrates within the available glycoproteome. The final glycosylation step in sialyl Lewis x and sialyl Lewis a biosynthesis in MKN45 cell line was shown to be associated to FUT5, which efficiently fucosylated sialyl Lewis precursors on glycoproteins. Moreover we demonstrate that the expression of sialyl Lewis epitopes in the MKN45 was induced by cell confluence, which can be regarded as a model to study altered glycosylation during tumour progression. This increase was observed together with an increase in mRNA levels of ST3GAL3, FUT5 and FUT6, and a decrease in FUT4 transcript levels in MKN45 confluent cells, suggesting a possible control at the transcriptional level.</description><subject>Antigens, Tumor-Associated, Carbohydrate - metabolism</subject><subject>Biochemistry, Molecular Biology</subject><subject>Cell confluence</subject><subject>Cell Count</subject><subject>Cell Extracts</subject><subject>Cell Line, Tumor</subject><subject>Fucosyltransferases - genetics</subject><subject>Fucosyltransferases - metabolism</subject><subject>Gastric cancer</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>mRNA expression</subject><subject>Oligosaccharides - metabolism</subject><subject>Sialyl Lewis a and sialyl Lewis x</subject><subject>Sialyltransferase</subject><subject>Sialyltransferases - genetics</subject><subject>Sialyltransferases - metabolism</subject><subject>Stomach Neoplasms - enzymology</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach Neoplasms - pathology</subject><subject>Transfection</subject><issn>1357-2725</issn><issn>1878-5875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc2KFDEQx4Mo7rr6BiK5ibA9m-p0-uMiLOvHCgNe9Bwy6cpuhp5kTHWPu48lvofPZNoeFD0IBSmqfvWvShVjz0GsQEB9sV1tfLQ4rEohutVsIB6wU2ibtlBtox5mX6qmKJtSnbAnRFshBKhSPmYn0DUt1DWcsu9vvHOYMIzeDBzv9gmJfAw8Ov7jW1Gey4Jy5n4YkwmUSUNI3IR-zsK5vKgKN9lI_wAJb6bBjNkbb5EPeMCBZslFi6_xq88qv3T-Ct1xH_iNoTFFH3L56EMey5pkfYg7w_N_B3rKHjkzED47vmfs87u3n66ui_XH9x-uLteFlZ0aC2VlD51AIWzZ1cq2rgSjaqe6ClWFxtV9iZ1sXdP2mbV2I1pQrnENYF1tjDxjrxbdWzPoffI7k-51NF5fX671HBOiKmVe4wEy-3Jh9yl-mfLgeudpntYEjBPpRlZQQytkJquFtCkSJXS_pUHo-bJ6q5fL6vmyejYQuezFscG02WH_p-h4ygy8XoC8ajx4TJqsx2Cx9wntqPvo_9_hJ14muq0</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Carvalho, A.S.</creator><creator>Harduin-Lepers, A.</creator><creator>Magalhães, A.</creator><creator>Machado, E.</creator><creator>Mendes, N.</creator><creator>Costa, L.T.</creator><creator>Matthiesen, R.</creator><creator>Almeida, R.</creator><creator>Costa, J.</creator><creator>Reis, C.A.</creator><general>Elsevier Ltd</general><general>Elsevier</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><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-1233-3799</orcidid><orcidid>https://orcid.org/0000-0003-2888-9617</orcidid></search><sort><creationdate>20100101</creationdate><title>Differential expression of α-2,3-sialyltransferases and α-1,3/4-fucosyltransferases regulates the levels of sialyl Lewis a and sialyl Lewis x in gastrointestinal carcinoma cells</title><author>Carvalho, A.S. ; Harduin-Lepers, A. ; Magalhães, A. ; Machado, E. ; Mendes, N. ; Costa, L.T. ; Matthiesen, R. ; Almeida, R. ; Costa, J. ; Reis, C.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-5c3d190e00c2965c8f21a56f594e54eaf6d2e938f78d5c3ccb0815f7f71e64ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Antigens, Tumor-Associated, Carbohydrate - metabolism</topic><topic>Biochemistry, Molecular Biology</topic><topic>Cell confluence</topic><topic>Cell Count</topic><topic>Cell Extracts</topic><topic>Cell Line, Tumor</topic><topic>Fucosyltransferases - genetics</topic><topic>Fucosyltransferases - metabolism</topic><topic>Gastric cancer</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>mRNA expression</topic><topic>Oligosaccharides - metabolism</topic><topic>Sialyl Lewis a and sialyl Lewis x</topic><topic>Sialyltransferase</topic><topic>Sialyltransferases - genetics</topic><topic>Sialyltransferases - metabolism</topic><topic>Stomach Neoplasms - enzymology</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach Neoplasms - pathology</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carvalho, A.S.</creatorcontrib><creatorcontrib>Harduin-Lepers, A.</creatorcontrib><creatorcontrib>Magalhães, A.</creatorcontrib><creatorcontrib>Machado, E.</creatorcontrib><creatorcontrib>Mendes, N.</creatorcontrib><creatorcontrib>Costa, L.T.</creatorcontrib><creatorcontrib>Matthiesen, R.</creatorcontrib><creatorcontrib>Almeida, R.</creatorcontrib><creatorcontrib>Costa, J.</creatorcontrib><creatorcontrib>Reis, C.A.</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><collection>Hyper Article en Ligne (HAL)</collection><jtitle>The international journal of biochemistry &amp; cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carvalho, A.S.</au><au>Harduin-Lepers, A.</au><au>Magalhães, A.</au><au>Machado, E.</au><au>Mendes, N.</au><au>Costa, L.T.</au><au>Matthiesen, R.</au><au>Almeida, R.</au><au>Costa, J.</au><au>Reis, C.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression of α-2,3-sialyltransferases and α-1,3/4-fucosyltransferases regulates the levels of sialyl Lewis a and sialyl Lewis x in gastrointestinal carcinoma cells</atitle><jtitle>The international journal of biochemistry &amp; cell biology</jtitle><addtitle>Int J Biochem Cell Biol</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>42</volume><issue>1</issue><spage>80</spage><epage>89</epage><pages>80-89</pages><issn>1357-2725</issn><eissn>1878-5875</eissn><abstract>Sialyl Lewis x and sialyl Lewis a expression depends on sialyltransferases and fucosyltransferases. In this study, we screened for major variations of sialyltransferases and fucosyltransferases involved in the synthesis and regulation of sialyl Lewis x and sialyl Lewis a epitopes in gastrointestinal carcinoma cells. Our results show that expression of ST3Gal IV in several gastrointestinal cell lines is correlated with the expression of sialyl Lewis x at the cell surface. ST3Gal IV overexpressed in the gastric MKN45 cell line, showed exclusive enzymatic activity towards glycoproteins containing terminal Galβ1-4GlcNAc structure. On the other hand, when ST3Gal III was overexpressed in MKN45, an increase in the expression levels of both sialyl Lewis epitopes was observed. ST3Gal III and ST3Gal IV lead to de novo synthesis of sialyl Lewis x determinant on different molecular weight glycoproteins of MKN45 cells suggesting that each enzyme used different substrates within the available glycoproteome. The final glycosylation step in sialyl Lewis x and sialyl Lewis a biosynthesis in MKN45 cell line was shown to be associated to FUT5, which efficiently fucosylated sialyl Lewis precursors on glycoproteins. Moreover we demonstrate that the expression of sialyl Lewis epitopes in the MKN45 was induced by cell confluence, which can be regarded as a model to study altered glycosylation during tumour progression. This increase was observed together with an increase in mRNA levels of ST3GAL3, FUT5 and FUT6, and a decrease in FUT4 transcript levels in MKN45 confluent cells, suggesting a possible control at the transcriptional level.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>19781661</pmid><doi>10.1016/j.biocel.2009.09.010</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1233-3799</orcidid><orcidid>https://orcid.org/0000-0003-2888-9617</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1357-2725
ispartof The international journal of biochemistry & cell biology, 2010-01, Vol.42 (1), p.80-89
issn 1357-2725
1878-5875
language eng
recordid cdi_hal_primary_oai_HAL_hal_00423661v1
source MEDLINE; Elsevier ScienceDirect Journals
subjects Antigens, Tumor-Associated, Carbohydrate - metabolism
Biochemistry, Molecular Biology
Cell confluence
Cell Count
Cell Extracts
Cell Line, Tumor
Fucosyltransferases - genetics
Fucosyltransferases - metabolism
Gastric cancer
Gene Expression Regulation, Enzymologic
Gene Expression Regulation, Neoplastic
Humans
Life Sciences
mRNA expression
Oligosaccharides - metabolism
Sialyl Lewis a and sialyl Lewis x
Sialyltransferase
Sialyltransferases - genetics
Sialyltransferases - metabolism
Stomach Neoplasms - enzymology
Stomach Neoplasms - genetics
Stomach Neoplasms - pathology
Transfection
title Differential expression of α-2,3-sialyltransferases and α-1,3/4-fucosyltransferases regulates the levels of sialyl Lewis a and sialyl Lewis x in gastrointestinal carcinoma cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T06%3A08%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Differential%20expression%20of%20%CE%B1-2,3-sialyltransferases%20and%20%CE%B1-1,3/4-fucosyltransferases%20regulates%20the%20levels%20of%20sialyl%20Lewis%20a%20and%20sialyl%20Lewis%20x%20in%20gastrointestinal%20carcinoma%20cells&rft.jtitle=The%20international%20journal%20of%20biochemistry%20&%20cell%20biology&rft.au=Carvalho,%20A.S.&rft.date=2010-01-01&rft.volume=42&rft.issue=1&rft.spage=80&rft.epage=89&rft.pages=80-89&rft.issn=1357-2725&rft.eissn=1878-5875&rft_id=info:doi/10.1016/j.biocel.2009.09.010&rft_dat=%3Cproquest_hal_p%3E734161803%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=734161803&rft_id=info:pmid/19781661&rft_els_id=S1357272509002660&rfr_iscdi=true