Evidence map›Paper›PMID 25611300›Full record

ArticleBritish journal of cancer2015

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.

R G Morgan, E Molnár, R F Jones, T J Collard, J D Lane, A Greenhough, C Paraskeva, A C Williams

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. The intellectual base and research fronts of LGR5: a bibliometric analysis.Frontiers in research metrics and analytics · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Immunohistochemical Analysis of the Stem Cell Marker LGR5 in Pediatric Liver Disease.Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

R G MorganCancer Research UK Colorectal Tumour Biology Group, School of Cellular and Molecular Medicine, Bristol BS8 1TD, UK.
E MolnárSchool of Physiology and Pharmacology, Bristol BS8 1TD, UK.
R F JonesCancer Research UK Colorectal Tumour Biology Group, School of Cellular and Molecular Medicine, Bristol BS8 1TD, UK.
T J CollardCancer Research UK Colorectal Tumour Biology Group, School of Cellular and Molecular Medicine, Bristol BS8 1TD, UK.
J D LaneCell Biology Laboratories, School of Biochemistry, University of Bristol, Medical Sciences Building, University Walk, Bristol BS8 1TD, UK.
A GreenhoughCancer Research UK Colorectal Tumour Biology Group, School of Cellular and Molecular Medicine, Bristol BS8 1TD, UK.
C ParaskevaCancer Research UK Colorectal Tumour Biology Group, School of Cellular and Molecular Medicine, Bristol BS8 1TD, UK.
A C WilliamsCancer Research UK Colorectal Tumour Biology Group, School of Cellular and Molecular Medicine, Bristol BS8 1TD, UK.
Cancer Research UK · GBAt Bristol · GBUniversity of Bristol · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J015938/1Cancer Research UK 11975Cancer Research UK C19/A11975
6 · The paper itself

Abstract

backgroundLGR5 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.

methodsNutrient 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.

resultsGlucose 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.

conclusionsNutrient 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.

Indexed as

AdenomaCell MembraneColorectal NeoplasmsFoodGlucoseGlycosylationHumansNeoplastic Stem CellsProtein StabilityProtein TransportReceptors, G-Protein-CoupledStress, PhysiologicalTumor Cells, CulturedTumor MicroenvironmentGlucoseLGR5 protein, humanReceptors, G-Protein-Coupled

Identifiers

PMID25611300
PMCPMC4333507
OpenAlexW2082135667

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.