Evidence map›Paper›PMID 41731278›Full record

ArticleMolecular imaging and biology2026

Imaging vascular characteristics and glycolytic metabolism of glioblastoma in a chick embryo model using

Elisabeth Non Gash, Jan Schulze, Sarah E Barnett, Mahon L Maguire, Michael Batie, Mohesh Moothanchery, Stephen Pickup, Ian Scott, Rasheed Zakaria, Judy M Coulson and 2 more

Abstract read
In one paragraph

Article in Molecular imaging and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Elisabeth Non GashDepartment of Molecular & Clinical Cancer Medicine, Institute of Systems, Molecular & Integrative Biology, University of Liverpool, Liverpool, UK.
Jan SchulzeDepartment of Molecular & Clinical Cancer Medicine, Institute of Systems, Molecular & Integrative Biology, University of Liverpool, Liverpool, UK.
Sarah E BarnettEgg Facility, Liverpool Shared Research Facility, University of Liverpool, Liverpool, UK.
Mahon L MaguireCentre for Pre-Clinical Imaging, Liverpool Shared Resource Facilities, University of Liverpool, Nuffield Wing, Sherrington Building, Crown Street, Liverpool, L69 3BX, UK.
Michael BatieDepartment of Biochemistry and Systems Biology, Institute of Systems, Molecular & Integrative Biology, University of Liverpool, Liverpool, UK.
Mohesh MoothancheryCentre for Pre-Clinical Imaging, Liverpool Shared Resource Facilities, University of Liverpool, Nuffield Wing, Sherrington Building, Crown Street, Liverpool, L69 3BX, UK.
Stephen PickupDepartment of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Ian ScottDepartment of Pathology, The Walton Centre NHS Trust, Liverpool, UK.
Rasheed ZakariaDepartment of Molecular & Clinical Cancer Medicine, Institute of Systems, Molecular & Integrative Biology, University of Liverpool, Liverpool, UK.
Judy M CoulsonDepartment of Molecular & Clinical Cancer Medicine, Institute of Systems, Molecular & Integrative Biology, University of Liverpool, Liverpool, UK.
Sonia RochaDepartment of Biochemistry and Systems Biology, Institute of Systems, Molecular & Integrative Biology, University of Liverpool, Liverpool, UK.
Harish PoptaniDepartment of Molecular & Clinical Cancer Medicine, Institute of Systems, Molecular & Integrative Biology, University of Liverpool, Liverpool, UK. harish.poptani@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-0593-3235

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo assess hypoxia-associated host-tumour vascular adaptations and glycolytic metabolism in the chick chorioallantoic membrane (CAM) glioblastoma model. PROCEDURES: U251 GBM cells were conditioned under normoxia (21% O₂) or hypoxia (1% O₂) for 72 h before implantation onto the CAM on embryonic day 7 (E7). Imaging was performed on E13 using MRI (control-CAM n = 8, normoxic-tumour n = 7, hypoxic-tumour n = 6) and brightfield microscopy (control-CAM n = 7, normoxic-tumour n = 8, hypoxic-tumour n = 7). Tumours were harvested on E14 for histology and gene expression analyses. In a separate cohort of 25 GBM-CAM tumours grown under normoxic conditioning, the correlation of glucose metabolism was assessed using [

resultsNormoxia- and hypoxia-conditioned tumour-bearing CAMs exhibited vascular remodelling and significant upregulation of VEGFA and ADM compared to cultured cells. αSMA staining confirmed vessel infiltration in normoxia-conditioned tumours. CAIX staining revealed a hypoxic core in these tumours while hypoxia-conditioned tumours displayed heterogeneous staining. In both conditions, GLUT1 staining colocalised with CAIX staining, indicating hypoxia-associated glycolysis. GLUT1, PDK1 and LDHA expression was elevated in CAM tumours relative to tumour cells in vitro. In the metabolic imaging cohort, most tumours exhibited [

conclusionsThe CAM model provides a versatile platform for investigating GBM vascularisation and metabolism. Hypoxic conditioning amplifies transcriptional and vascular changes to the CAM. Although both [

Indexed as

Fluorodeoxyglucose F18GlioblastomaGlycolysisMagnetic Resonance ImagingPositron-Emission TomographyAnimalsCell Line, TumorChick EmbryoChorioallantoic MembraneHumansNeovascularization, PathologicFluorodeoxyglucose F18Chick chorioallantoic membraneGlioblastomaMetabolismMRIPETVasculature

Identifiers

PMID41731278
PMCPMC13161295

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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.