Brain Cancer Research, Neurosurgery Department, Chris O'Brien Lifehouse, Camperdown, NSW, Australia.
Department of Neuropathology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
Br J Cancer. 2024 Mar;130(5):836-851. doi: 10.1038/s41416-023-02548-9. Epub 2024 Jan 11.
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.
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).
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).
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.
急需反映胶质母细胞瘤肿瘤活性和治疗反应的生物标志物来帮助指导临床管理,特别是对于复发性疾病。由于泌尿系统是循环细胞外囊泡(EV;30-1000nm 纳米颗粒)的主要清除途径,我们探讨了是否可以通过采集尿液中的 EV 作为一种简单、非侵入性的液体活检方法来测量与胶质母细胞瘤相关的生物标志物。
从 24 例经导管的胶质母细胞瘤患者中收集了 50 份尿液标本(15-60ml),这些患者在初次(n=17)和复发(n=7)手术前、全切除术后(n=9)和年龄/性别匹配的健康参与者(n=14)。通过差速超速离心分离 EV,通过高分辨率数据非依赖性采集液相色谱串联质谱(DIA-LC-MS/MS)分析提取的蛋白质组。
总体而言,在尿 EV 中鉴定出 6857 种蛋白(q 值≤0.01),包括 94 种 EV 标记蛋白。确定了胶质母细胞瘤特异性的蛋白质组学特征,并鉴定出与肿瘤负荷和复发相对应的潜在尿 EV 生物标志物(FC≥|2|,调整后的 p 值≤0.05,AUC>0.9)。
对尿 EV 进行深入的 DIA-LC-MS/MS 表征证实了尿液是胶质母细胞瘤生物标志物的可行来源。这里描述的有前途的“液体黄金”生物标志物组合值得进一步研究。