Glioblastoma biomarkers in urinary extracellular vesicles reveal the potential for a ‘liquid gold’ biopsy

Background Biomarkers that reflect glioblastoma tumour activity and treatment response are urgently needed to help guide clinical management, particularly for recurrent disease. As the urinary system is a major clearance route of circulating extracellular vesicles (EVs; 30–1000 nm nanoparticles) we...

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Veröffentlicht in:British journal of cancer 2024-03, Vol.130 (5), p.836-851
Hauptverfasser: Hallal, Susannah M., Tűzesi, Ágota, Sida, Liam A., Xian, Elissa, Madani, Daniel, Muralidharan, Krishna, Shivalingam, Brindha, Buckland, Michael E., Satgunaseelan, Laveniya, Alexander, Kimberley L.
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Sprache:eng
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Zusammenfassung:Background Biomarkers that reflect glioblastoma tumour activity and treatment response are urgently needed to help guide clinical management, particularly for recurrent disease. As the urinary system is a major clearance route of circulating extracellular vesicles (EVs; 30–1000 nm nanoparticles) we explored whether sampling urinary-EVs could serve as a simple and non-invasive liquid biopsy approach for measuring glioblastoma-associated biomarkers. Methods Fifty urine specimens (15–60 ml) were collected from 24 catheterised glioblastoma patients immediately prior to primary ( n  = 17) and recurrence ( n  = 7) surgeries, following gross total resection ( n  = 9), and from age/gender-matched healthy participants ( n  = 14). EVs isolated by differential ultracentrifugation were characterised and extracted proteomes were analysed by high-resolution data-independent acquisition liquid chromatography tandem mass spectrometry (DIA-LC-MS/MS). Results Overall, 6857 proteins were confidently identified in urinary-EVs ( q -value ≤ 0.01), including 94 EV marker proteins. Glioblastoma-specific proteomic signatures were determined, and putative urinary-EV biomarkers corresponding to tumour burden and recurrence were identified (FC ≥ | 2 | , adjust p -val≤0.05, AUC > 0.9). Conclusion In-depth DIA-LC-MS/MS characterisation of urinary-EVs substantiates urine as a viable source of glioblastoma biomarkers. The promising ‘liquid gold’ biomarker panels described here warrant further investigation.
ISSN:0007-0920
1532-1827
DOI:10.1038/s41416-023-02548-9