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
Hauptverfasser: Morgan, R G, Molnár, E, Jones, R F, Collard, T J, Lane, J D, Greenhough, A, Paraskeva, C, Williams, A C
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container_end_page 719
container_issue 4
container_start_page 714
container_title British journal of cancer
container_volume 112
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
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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. 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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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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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