Nutrient stress alters the glycosylation status of LGR5 resulting in reduced protein stability and membrane localisation in colorectal tumour cells: implications for targeting cancer stem cells
Background: LGR5 is an important marker of intestinal stem cells and performs its vital functions at the cell membrane. Despite the importance of LGR5 to both normal and cancer stem cell biology, it is not known how microenvironmental stress affects the expression and subcellular distribution of the...
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Veröffentlicht in: | British journal of cancer 2015-02, Vol.112 (4), p.714-719 |
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creator | Morgan, R G Molnár, E Jones, R F Collard, T J Lane, J D Greenhough, A Paraskeva, C Williams, A C |
description | Background:
LGR5 is an important marker of intestinal stem cells and performs its vital functions at the cell membrane. Despite the importance of LGR5 to both normal and cancer stem cell biology, it is not known how microenvironmental stress affects the expression and subcellular distribution of the protein.
Methods:
Nutrient stress was induced through glucose starvation. Glycosylation status was assessed using endoglycosidase or tunicamycin treatment. Flow cytometry and confocal microscopy were used to assess subcellular distribution of LGR5.
Results:
Glucose deprivation altered the glycosylation status of LGR5 resulting in reduced protein stability and cell surface expression. Furthermore, inhibiting LGR5 glycosylation resulted in depleted surface expression and reduced localisation in the
cis
-Golgi network.
Conclusions:
Nutrient stress within a tumour microenvironment has the capacity to alter LGR5 protein stability and membrane localisation through modulation of LGR5 glycosylation status. As LGR5 surface localisation is required for enhanced Wnt signalling, this is the first report to show a mechanism by which the microenvironment could affect LGR5 function. |
doi_str_mv | 10.1038/bjc.2015.4 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4333507</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1657324691</sourcerecordid><originalsourceid>FETCH-LOGICAL-c442t-15e782e33c342f166439989b3d918f9fe3e4a15982708936050e4d28d923c90d3</originalsourceid><addsrcrecordid>eNplkt2KFDEQhYMo7jh64wNIwBtResxP_8ULQRZdhUFB9Dqk09W9GdLJmKSFeTzfzPT0uqx6VRT1carqcBB6SsmOEt6-7g56xwitduU9tKEVZwVtWXMfbQghTUEEIxfoUYyH3ArSNg_RBatqSjkhG_Tr85yCAZdwTAFixMomCBGna8CjPWkfT1Yl412eqzRH7Ae8v_pa4QzPNhk3YuNy088aenwMPoE5s52xJp2wcj2eYOqCcoCt18qauOplTHvrA-ikLE7z5OeANVgb32AzHa3RZy7iwQecVBjhvE0rpyHkDTCt9GP0YFA2wpObukXfP7z_dvmx2H-5-nT5bl_osmSpoBU0LQPONS_ZQOu65EK0ouO9oO0gBuBQKlqJ7BxpBa9JRaDsWdsLxrUgPd-it6vuce4m6HX2LCgrj8FMKpykV0b-PXHmWo7-pyw55xVpssCLG4Hgf8wQk5xMXF7I1vg5SlpXDWdlLWhGn_-DHrI7Lr-3UFXDaioWwZcrpYOPMcBwewwlckmGzMmQSzLyDVv07O75t-ifKGTg1QrEPHIjhDs7_5f7DeWPx24</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1655726197</pqid></control><display><type>article</type><title>Nutrient stress alters the glycosylation status of LGR5 resulting in reduced protein stability and membrane localisation in colorectal tumour cells: implications for targeting cancer stem cells</title><source>MEDLINE</source><source>Nature</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>SpringerLink Journals - AutoHoldings</source><creator>Morgan, R G ; Molnár, E ; Jones, R F ; Collard, T J ; Lane, J D ; Greenhough, A ; Paraskeva, C ; Williams, A C</creator><creatorcontrib>Morgan, R G ; Molnár, E ; Jones, R F ; Collard, T J ; Lane, J D ; Greenhough, A ; Paraskeva, C ; Williams, A C</creatorcontrib><description>Background:
LGR5 is an important marker of intestinal stem cells and performs its vital functions at the cell membrane. Despite the importance of LGR5 to both normal and cancer stem cell biology, it is not known how microenvironmental stress affects the expression and subcellular distribution of the protein.
Methods:
Nutrient stress was induced through glucose starvation. Glycosylation status was assessed using endoglycosidase or tunicamycin treatment. Flow cytometry and confocal microscopy were used to assess subcellular distribution of LGR5.
Results:
Glucose deprivation altered the glycosylation status of LGR5 resulting in reduced protein stability and cell surface expression. Furthermore, inhibiting LGR5 glycosylation resulted in depleted surface expression and reduced localisation in the
cis
-Golgi network.
Conclusions:
Nutrient stress within a tumour microenvironment has the capacity to alter LGR5 protein stability and membrane localisation through modulation of LGR5 glycosylation status. As LGR5 surface localisation is required for enhanced Wnt signalling, this is the first report to show a mechanism by which the microenvironment could affect LGR5 function.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.2015.4</identifier><identifier>PMID: 25611300</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/337/458/1524 ; 631/45/612/194 ; 692/699/67/1504/1885 ; 692/699/67/327 ; Adenoma - genetics ; Adenoma - metabolism ; Adenoma - therapy ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Cell Membrane - metabolism ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - therapy ; Drug Resistance ; Epidemiology ; Food ; Glucose - deficiency ; Glycosylation ; Humans ; Molecular Medicine ; Neoplastic Stem Cells - metabolism ; Oncology ; Protein Stability ; Protein Transport ; Receptors, G-Protein-Coupled - genetics ; Receptors, G-Protein-Coupled - metabolism ; Short Communication ; Stress, Physiological - physiology ; Tumor Cells, Cultured ; Tumor Microenvironment</subject><ispartof>British journal of cancer, 2015-02, Vol.112 (4), p.714-719</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Feb 17, 2015</rights><rights>Copyright © 2015 Cancer Research UK 2015 Cancer Research UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-15e782e33c342f166439989b3d918f9fe3e4a15982708936050e4d28d923c90d3</citedby><cites>FETCH-LOGICAL-c442t-15e782e33c342f166439989b3d918f9fe3e4a15982708936050e4d28d923c90d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333507/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333507/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25611300$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morgan, R G</creatorcontrib><creatorcontrib>Molnár, E</creatorcontrib><creatorcontrib>Jones, R F</creatorcontrib><creatorcontrib>Collard, T J</creatorcontrib><creatorcontrib>Lane, J D</creatorcontrib><creatorcontrib>Greenhough, A</creatorcontrib><creatorcontrib>Paraskeva, C</creatorcontrib><creatorcontrib>Williams, A C</creatorcontrib><title>Nutrient stress alters the glycosylation status of LGR5 resulting in reduced protein stability and membrane localisation in colorectal tumour cells: implications for targeting cancer stem cells</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>Background:
LGR5 is an important marker of intestinal stem cells and performs its vital functions at the cell membrane. Despite the importance of LGR5 to both normal and cancer stem cell biology, it is not known how microenvironmental stress affects the expression and subcellular distribution of the protein.
Methods:
Nutrient stress was induced through glucose starvation. Glycosylation status was assessed using endoglycosidase or tunicamycin treatment. Flow cytometry and confocal microscopy were used to assess subcellular distribution of LGR5.
Results:
Glucose deprivation altered the glycosylation status of LGR5 resulting in reduced protein stability and cell surface expression. Furthermore, inhibiting LGR5 glycosylation resulted in depleted surface expression and reduced localisation in the
cis
-Golgi network.
Conclusions:
Nutrient stress within a tumour microenvironment has the capacity to alter LGR5 protein stability and membrane localisation through modulation of LGR5 glycosylation status. As LGR5 surface localisation is required for enhanced Wnt signalling, this is the first report to show a mechanism by which the microenvironment could affect LGR5 function.</description><subject>631/337/458/1524</subject><subject>631/45/612/194</subject><subject>692/699/67/1504/1885</subject><subject>692/699/67/327</subject><subject>Adenoma - genetics</subject><subject>Adenoma - metabolism</subject><subject>Adenoma - therapy</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Cell Membrane - metabolism</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - therapy</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Food</subject><subject>Glucose - deficiency</subject><subject>Glycosylation</subject><subject>Humans</subject><subject>Molecular Medicine</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Oncology</subject><subject>Protein Stability</subject><subject>Protein Transport</subject><subject>Receptors, G-Protein-Coupled - genetics</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Short Communication</subject><subject>Stress, Physiological - physiology</subject><subject>Tumor Cells, Cultured</subject><subject>Tumor Microenvironment</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNplkt2KFDEQhYMo7jh64wNIwBtResxP_8ULQRZdhUFB9Dqk09W9GdLJmKSFeTzfzPT0uqx6VRT1carqcBB6SsmOEt6-7g56xwitduU9tKEVZwVtWXMfbQghTUEEIxfoUYyH3ArSNg_RBatqSjkhG_Tr85yCAZdwTAFixMomCBGna8CjPWkfT1Yl412eqzRH7Ae8v_pa4QzPNhk3YuNy088aenwMPoE5s52xJp2wcj2eYOqCcoCt18qauOplTHvrA-ikLE7z5OeANVgb32AzHa3RZy7iwQecVBjhvE0rpyHkDTCt9GP0YFA2wpObukXfP7z_dvmx2H-5-nT5bl_osmSpoBU0LQPONS_ZQOu65EK0ouO9oO0gBuBQKlqJ7BxpBa9JRaDsWdsLxrUgPd-it6vuce4m6HX2LCgrj8FMKpykV0b-PXHmWo7-pyw55xVpssCLG4Hgf8wQk5xMXF7I1vg5SlpXDWdlLWhGn_-DHrI7Lr-3UFXDaioWwZcrpYOPMcBwewwlckmGzMmQSzLyDVv07O75t-ifKGTg1QrEPHIjhDs7_5f7DeWPx24</recordid><startdate>20150217</startdate><enddate>20150217</enddate><creator>Morgan, R G</creator><creator>Molnár, E</creator><creator>Jones, R F</creator><creator>Collard, T J</creator><creator>Lane, J D</creator><creator>Greenhough, A</creator><creator>Paraskeva, C</creator><creator>Williams, A C</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150217</creationdate><title>Nutrient stress alters the glycosylation status of LGR5 resulting in reduced protein stability and membrane localisation in colorectal tumour cells: implications for targeting cancer stem cells</title><author>Morgan, R G ; Molnár, E ; Jones, R F ; Collard, T J ; Lane, J D ; Greenhough, A ; Paraskeva, C ; Williams, A C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-15e782e33c342f166439989b3d918f9fe3e4a15982708936050e4d28d923c90d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>631/337/458/1524</topic><topic>631/45/612/194</topic><topic>692/699/67/1504/1885</topic><topic>692/699/67/327</topic><topic>Adenoma - genetics</topic><topic>Adenoma - metabolism</topic><topic>Adenoma - therapy</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Cell Membrane - metabolism</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Colorectal Neoplasms - therapy</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Food</topic><topic>Glucose - deficiency</topic><topic>Glycosylation</topic><topic>Humans</topic><topic>Molecular Medicine</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Oncology</topic><topic>Protein Stability</topic><topic>Protein Transport</topic><topic>Receptors, G-Protein-Coupled - genetics</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Short Communication</topic><topic>Stress, Physiological - physiology</topic><topic>Tumor Cells, Cultured</topic><topic>Tumor Microenvironment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morgan, R G</creatorcontrib><creatorcontrib>Molnár, E</creatorcontrib><creatorcontrib>Jones, R F</creatorcontrib><creatorcontrib>Collard, T J</creatorcontrib><creatorcontrib>Lane, J D</creatorcontrib><creatorcontrib>Greenhough, A</creatorcontrib><creatorcontrib>Paraskeva, C</creatorcontrib><creatorcontrib>Williams, A C</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morgan, R G</au><au>Molnár, E</au><au>Jones, R F</au><au>Collard, T J</au><au>Lane, J D</au><au>Greenhough, A</au><au>Paraskeva, C</au><au>Williams, A C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nutrient stress alters the glycosylation status of LGR5 resulting in reduced protein stability and membrane localisation in colorectal tumour cells: implications for targeting cancer stem cells</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><addtitle>Br J Cancer</addtitle><date>2015-02-17</date><risdate>2015</risdate><volume>112</volume><issue>4</issue><spage>714</spage><epage>719</epage><pages>714-719</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>Background:
LGR5 is an important marker of intestinal stem cells and performs its vital functions at the cell membrane. Despite the importance of LGR5 to both normal and cancer stem cell biology, it is not known how microenvironmental stress affects the expression and subcellular distribution of the protein.
Methods:
Nutrient stress was induced through glucose starvation. Glycosylation status was assessed using endoglycosidase or tunicamycin treatment. Flow cytometry and confocal microscopy were used to assess subcellular distribution of LGR5.
Results:
Glucose deprivation altered the glycosylation status of LGR5 resulting in reduced protein stability and cell surface expression. Furthermore, inhibiting LGR5 glycosylation resulted in depleted surface expression and reduced localisation in the
cis
-Golgi network.
Conclusions:
Nutrient stress within a tumour microenvironment has the capacity to alter LGR5 protein stability and membrane localisation through modulation of LGR5 glycosylation status. As LGR5 surface localisation is required for enhanced Wnt signalling, this is the first report to show a mechanism by which the microenvironment could affect LGR5 function.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>25611300</pmid><doi>10.1038/bjc.2015.4</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Nature; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; SpringerLink Journals - AutoHoldings |
subjects | 631/337/458/1524 631/45/612/194 692/699/67/1504/1885 692/699/67/327 Adenoma - genetics Adenoma - metabolism Adenoma - therapy Biomedical and Life Sciences Biomedicine Cancer Research Cell Membrane - metabolism Colorectal Neoplasms - genetics Colorectal Neoplasms - metabolism Colorectal Neoplasms - therapy Drug Resistance Epidemiology Food Glucose - deficiency Glycosylation Humans Molecular Medicine Neoplastic Stem Cells - metabolism Oncology Protein Stability Protein Transport Receptors, G-Protein-Coupled - genetics Receptors, G-Protein-Coupled - metabolism Short Communication Stress, Physiological - physiology Tumor Cells, Cultured Tumor Microenvironment |
title | Nutrient stress alters the glycosylation status of LGR5 resulting in reduced protein stability and membrane localisation in colorectal tumour cells: implications for targeting cancer stem cells |
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