ANALYSING THE ROLE OF GLUT-1 AND GLUT-3 PROTEINS IN HISTONE 3 MUTATED CHILDHOOD BRAIN TUMOUR

Abstract AIMS Paediatric high-grade gliomas (pHGG) are the leading cause of childhood cancer deaths. A subset of pHGG has Histone 3 (H3) mutation in them, mainly H3-K27M, H3-G34R, H3-G34V mutations. Our previous research has found increased expression of cell membrane proteins, GLUT-1 (Glucose transport) and GLUT-3 in H3 mutated pHGG. The aim of this study is to analyse the role of GLUT-1 and GLUT-3 in H3 mutated pHGG by localization, expression and inhibiting their function these with drugs/small molecules. METHODS Expression and localization study of GLUT-1 and GLUT-3 proteins in different pHGG cultured cell-lines and controls, was carried out by immunofluorescence and western-blot experiments. Inhibition of GLUT-1 and GLUT-3 by Glutor measured by cell proliferation assays and analyses. RESULTS Immunofluorescence and western blot experiments revealed increased expression of GLUT-3 protein in pHGG cell lines than control astrocytes. Although over-expressed, GLUT-1 was less varied in expression than GLUT-3. Results of the above experiments and inhibitory effect of Glutor will be presented. CONCLUSION The study provides insight into the potential role of GLUT-1 and GLUT-3 proteins in H3 mutated pHGG and highlights areas for further research and could be targets for future therapeutics.

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Publication Details

Journal
Neuro-Oncology
Published
2025-09-01
DOI
https://doi.org/10.1093/neuonc/noaf185.047
Primary Topic
RNA modifications and cancer
Type
article
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article

ANALYSING THE ROLE OF GLUT-1 AND GLUT-3 PROTEINS IN HISTONE 3 MUTATED CHILDHOOD BRAIN TUMOUR

Robert Layfield, Anya Snary, Farhana Haque, Parsa Samimi
Neuro-Oncology
RNA modifications and cancer
article

ANALYSING THE ROLE OF GLUT-1 AND GLUT-3 PROTEINS IN HISTONE 3 MUTATED CHILDHOOD BRAIN TUMOUR

Robert Layfield, Anya Snary, Farhana Haque, Parsa Samimi
article en

Abstract

Abstract AIMS Paediatric high-grade gliomas (pHGG) are the leading cause of childhood cancer deaths. A subset of pHGG has Histone 3 (H3) mutation in them, mainly H3-K27M, H3-G34R, H3-G34V mutations. Our previous research has found increased expression of cell membrane proteins, GLUT-1 (Glucose transport) and GLUT-3 in H3 mutated pHGG. The aim of this study is to analyse the role of GLUT-1 and GLUT-3 in H3 mutated pHGG by localization, expression and inhibiting their function these with drugs/small molecules. METHODS Expression and localization study of GLUT-1 and GLUT-3 proteins in different pHGG cultured cell-lines and controls, was carried out by immunofluorescence and western-blot experiments. Inhibition of GLUT-1 and GLUT-3 by Glutor measured by cell proliferation assays and analyses. RESULTS Immunofluorescence and western blot experiments revealed increased expression of GLUT-3 protein in pHGG cell lines than control astrocytes. Although over-expressed, GLUT-1 was less varied in expression than GLUT-3. Results of the above experiments and inhibitory effect of Glutor will be presented. CONCLUSION The study provides insight into the potential role of GLUT-1 and GLUT-3 proteins in H3 mutated pHGG and highlights areas for further research and could be targets for future therapeutics.

Neuro-OncologyVol. 27(Supplement_2)
University of Nottingham (GB), University of Lincoln (GB), Nottingham Trent University (GB)
Openalex Percentile: Top 79%
RNA modifications and cancer
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