Comprehensive Analysis of Oligo/Polysialylglycoconjugates in Cancer Cell Lines
In cancer cells, cell-surface sialylation is altered, including a change in oligo/polysialic acid (oligo/polySia) structures. Since they are unique and rarely expressed in normal cells, oligo/polySia structures may serve as promising novel biomarkers and targets for therapies. For the diagnosis and...
Gespeichert in:
Veröffentlicht in: | International journal of molecular sciences 2022-05, Vol.23 (10), p.5569 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 10 |
container_start_page | 5569 |
container_title | International journal of molecular sciences |
container_volume | 23 |
creator | Hane, Masaya Kitajima, Ken Sato, Chihiro |
description | In cancer cells, cell-surface sialylation is altered, including a change in oligo/polysialic acid (oligo/polySia) structures. Since they are unique and rarely expressed in normal cells, oligo/polySia structures may serve as promising novel biomarkers and targets for therapies. For the diagnosis and treatment of the disease, a precise understanding of the oligo/polySia structures in cancer cells is necessary. In this study, flow cytometric analysis and gene expression datasets were obtained from sixteen different cancer cell lines. These datasets demonstrated the ability to predict glycan structures and their sialylation status. Our results also revealed that sialylation patterns are unique to each cancer cell line. Thus, we can suggest promising combinations of antibody and cancer cell for glycan prediction. However, the precise prediction of minor glycans need to be further explored. |
doi_str_mv | 10.3390/ijms23105569 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9147586</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2671269248</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3939-109ed9d68b86e2e6867e5f2b419530a72403f22473b4fdb318b0c41c0978fe713</originalsourceid><addsrcrecordid>eNpdkctLxDAQxoMovm-epeDFg9U82jS5CEvxBYt60HNI02nN0iZrsl3Y_96uL1ZPM8z8-JhvPoROCL5kTOIrO-sjZQTnOZdbaJ9klKYY82J7o99DBzHOMKaM5nIX7bGcU8EE3UePpe_nAd7ARbuEZOJ0t4o2Jr5Jnjrb-qtnvx6M067tVsYb72ZDqxcQE-uSUjsDISmh65KpdRCP0E6juwjH3_UQvd7evJT36fTp7qGcTFPDJJMpwRJqWXNRCQ4UuOAF5A2tMiJzhnVBM8waSrOCVVlTV4yICpuMGCwL0UBB2CG6_tKdD1UPtQG3CLpT82B7HVbKa6v-bpx9U61fKkmyIhd8FDj_Fgj-fYC4UL2NZvShHfghKsoLQrmkmRjRs3_ozA9hfNQnhYkk430jdfFFmeBjDND8HkOwWgelNoMa8dNNA7_wTzLsA9tdjsg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2670191318</pqid></control><display><type>article</type><title>Comprehensive Analysis of Oligo/Polysialylglycoconjugates in Cancer Cell Lines</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Hane, Masaya ; Kitajima, Ken ; Sato, Chihiro</creator><creatorcontrib>Hane, Masaya ; Kitajima, Ken ; Sato, Chihiro</creatorcontrib><description>In cancer cells, cell-surface sialylation is altered, including a change in oligo/polysialic acid (oligo/polySia) structures. Since they are unique and rarely expressed in normal cells, oligo/polySia structures may serve as promising novel biomarkers and targets for therapies. For the diagnosis and treatment of the disease, a precise understanding of the oligo/polySia structures in cancer cells is necessary. In this study, flow cytometric analysis and gene expression datasets were obtained from sixteen different cancer cell lines. These datasets demonstrated the ability to predict glycan structures and their sialylation status. Our results also revealed that sialylation patterns are unique to each cancer cell line. Thus, we can suggest promising combinations of antibody and cancer cell for glycan prediction. However, the precise prediction of minor glycans need to be further explored.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23105569</identifier><identifier>PMID: 35628382</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Acids ; Antibodies ; Biomarkers ; Biosynthesis ; Cancer ; Cell surface ; Datasets ; Enzymes ; Flow cytometry ; Gene expression ; Gene flow ; Glycan ; Glycoproteins ; Hypoxia ; Neuroblastoma ; Polysaccharides ; Polysialic acid ; Tumor cell lines</subject><ispartof>International journal of molecular sciences, 2022-05, Vol.23 (10), p.5569</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3939-109ed9d68b86e2e6867e5f2b419530a72403f22473b4fdb318b0c41c0978fe713</citedby><cites>FETCH-LOGICAL-c3939-109ed9d68b86e2e6867e5f2b419530a72403f22473b4fdb318b0c41c0978fe713</cites><orcidid>0000-0002-2075-6185 ; 0000-0001-6830-2900</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147586/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147586/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35628382$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hane, Masaya</creatorcontrib><creatorcontrib>Kitajima, Ken</creatorcontrib><creatorcontrib>Sato, Chihiro</creatorcontrib><title>Comprehensive Analysis of Oligo/Polysialylglycoconjugates in Cancer Cell Lines</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>In cancer cells, cell-surface sialylation is altered, including a change in oligo/polysialic acid (oligo/polySia) structures. Since they are unique and rarely expressed in normal cells, oligo/polySia structures may serve as promising novel biomarkers and targets for therapies. For the diagnosis and treatment of the disease, a precise understanding of the oligo/polySia structures in cancer cells is necessary. In this study, flow cytometric analysis and gene expression datasets were obtained from sixteen different cancer cell lines. These datasets demonstrated the ability to predict glycan structures and their sialylation status. Our results also revealed that sialylation patterns are unique to each cancer cell line. Thus, we can suggest promising combinations of antibody and cancer cell for glycan prediction. However, the precise prediction of minor glycans need to be further explored.</description><subject>Acids</subject><subject>Antibodies</subject><subject>Biomarkers</subject><subject>Biosynthesis</subject><subject>Cancer</subject><subject>Cell surface</subject><subject>Datasets</subject><subject>Enzymes</subject><subject>Flow cytometry</subject><subject>Gene expression</subject><subject>Gene flow</subject><subject>Glycan</subject><subject>Glycoproteins</subject><subject>Hypoxia</subject><subject>Neuroblastoma</subject><subject>Polysaccharides</subject><subject>Polysialic acid</subject><subject>Tumor cell lines</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkctLxDAQxoMovm-epeDFg9U82jS5CEvxBYt60HNI02nN0iZrsl3Y_96uL1ZPM8z8-JhvPoROCL5kTOIrO-sjZQTnOZdbaJ9klKYY82J7o99DBzHOMKaM5nIX7bGcU8EE3UePpe_nAd7ARbuEZOJ0t4o2Jr5Jnjrb-qtnvx6M067tVsYb72ZDqxcQE-uSUjsDISmh65KpdRCP0E6juwjH3_UQvd7evJT36fTp7qGcTFPDJJMpwRJqWXNRCQ4UuOAF5A2tMiJzhnVBM8waSrOCVVlTV4yICpuMGCwL0UBB2CG6_tKdD1UPtQG3CLpT82B7HVbKa6v-bpx9U61fKkmyIhd8FDj_Fgj-fYC4UL2NZvShHfghKsoLQrmkmRjRs3_ozA9hfNQnhYkk430jdfFFmeBjDND8HkOwWgelNoMa8dNNA7_wTzLsA9tdjsg</recordid><startdate>20220516</startdate><enddate>20220516</enddate><creator>Hane, Masaya</creator><creator>Kitajima, Ken</creator><creator>Sato, Chihiro</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2075-6185</orcidid><orcidid>https://orcid.org/0000-0001-6830-2900</orcidid></search><sort><creationdate>20220516</creationdate><title>Comprehensive Analysis of Oligo/Polysialylglycoconjugates in Cancer Cell Lines</title><author>Hane, Masaya ; Kitajima, Ken ; Sato, Chihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3939-109ed9d68b86e2e6867e5f2b419530a72403f22473b4fdb318b0c41c0978fe713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acids</topic><topic>Antibodies</topic><topic>Biomarkers</topic><topic>Biosynthesis</topic><topic>Cancer</topic><topic>Cell surface</topic><topic>Datasets</topic><topic>Enzymes</topic><topic>Flow cytometry</topic><topic>Gene expression</topic><topic>Gene flow</topic><topic>Glycan</topic><topic>Glycoproteins</topic><topic>Hypoxia</topic><topic>Neuroblastoma</topic><topic>Polysaccharides</topic><topic>Polysialic acid</topic><topic>Tumor cell lines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hane, Masaya</creatorcontrib><creatorcontrib>Kitajima, Ken</creatorcontrib><creatorcontrib>Sato, Chihiro</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hane, Masaya</au><au>Kitajima, Ken</au><au>Sato, Chihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comprehensive Analysis of Oligo/Polysialylglycoconjugates in Cancer Cell Lines</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2022-05-16</date><risdate>2022</risdate><volume>23</volume><issue>10</issue><spage>5569</spage><pages>5569-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>In cancer cells, cell-surface sialylation is altered, including a change in oligo/polysialic acid (oligo/polySia) structures. Since they are unique and rarely expressed in normal cells, oligo/polySia structures may serve as promising novel biomarkers and targets for therapies. For the diagnosis and treatment of the disease, a precise understanding of the oligo/polySia structures in cancer cells is necessary. In this study, flow cytometric analysis and gene expression datasets were obtained from sixteen different cancer cell lines. These datasets demonstrated the ability to predict glycan structures and their sialylation status. Our results also revealed that sialylation patterns are unique to each cancer cell line. Thus, we can suggest promising combinations of antibody and cancer cell for glycan prediction. However, the precise prediction of minor glycans need to be further explored.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35628382</pmid><doi>10.3390/ijms23105569</doi><orcidid>https://orcid.org/0000-0002-2075-6185</orcidid><orcidid>https://orcid.org/0000-0001-6830-2900</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2022-05, Vol.23 (10), p.5569 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9147586 |
source | MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Acids Antibodies Biomarkers Biosynthesis Cancer Cell surface Datasets Enzymes Flow cytometry Gene expression Gene flow Glycan Glycoproteins Hypoxia Neuroblastoma Polysaccharides Polysialic acid Tumor cell lines |
title | Comprehensive Analysis of Oligo/Polysialylglycoconjugates in Cancer Cell Lines |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T07%3A16%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Comprehensive%20Analysis%20of%20Oligo/Polysialylglycoconjugates%20in%20Cancer%20Cell%20Lines&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Hane,%20Masaya&rft.date=2022-05-16&rft.volume=23&rft.issue=10&rft.spage=5569&rft.pages=5569-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms23105569&rft_dat=%3Cproquest_pubme%3E2671269248%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2670191318&rft_id=info:pmid/35628382&rfr_iscdi=true |