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Glioblastoma biomarkers in urinary extracellular vesicles reveal the potential for a 'liquid gold' biopsy.
Hallal, Susannah M; Tuzesi, Ágota; Sida, Liam A; Xian, Elissa; Madani, Daniel; Muralidharan, Krishna; Shivalingam, Brindha; Buckland, Michael E; Satgunaseelan, Laveniya; Alexander, Kimberley L.
Afiliação
  • Hallal SM; Brain Cancer Research, Neurosurgery Department, Chris O'Brien Lifehouse, Camperdown, NSW, Australia.
  • Tuzesi Á; Department of Neuropathology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
  • Sida LA; School of Medical Sciences, Faculty of Medicine and Health Sciences, The University of Sydney, Camperdown, NSW, Australia.
  • Xian E; Department of Neuropathology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
  • Madani D; School of Medical Sciences, Faculty of Medicine and Health Sciences, The University of Sydney, Camperdown, NSW, Australia.
  • Muralidharan K; School of Medical Sciences, Faculty of Medicine and Health Sciences, The University of Sydney, Camperdown, NSW, Australia.
  • Shivalingam B; Brain Cancer Research, Neurosurgery Department, Chris O'Brien Lifehouse, Camperdown, NSW, Australia.
  • Buckland ME; Neurosurgery Department, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
  • Satgunaseelan L; Brain Cancer Research, Neurosurgery Department, Chris O'Brien Lifehouse, Camperdown, NSW, Australia.
  • Alexander KL; Neurosurgery Department, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
Br J Cancer ; 130(5): 836-851, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38212481
ABSTRACT

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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glioblastoma / Vesículas Extracelulares Limite: Humans Idioma: En Revista: Br J Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glioblastoma / Vesículas Extracelulares Limite: Humans Idioma: En Revista: Br J Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália