Definition of an Inflammatory Biomarker Signature in Plasma-Derived Extracellular Vesicles of Glioblastoma Patients

被引:23
作者
Cilibrasi, Chiara [1 ]
Simon, Thomas [1 ,2 ]
Vintu, Marian [1 ,3 ]
Tolias, Christos [1 ,3 ]
Samuels, Mark [1 ]
Mazarakis, Nektarios K. [4 ,5 ]
Eravci, Murat [1 ]
Stewart, Nicolas [6 ]
Critchley, Giles [3 ]
Giamas, Georgios [1 ]
机构
[1] Univ Sussex, Sch Life Sci, Dept Biochem & Biomed, Brighton BN1 9QG, E Sussex, England
[2] Univ Southern Calif, Keck Sch Med, Dept Translat Genom, Los Angeles, CA 90033 USA
[3] Univ Hosp Sussex, Dept Neurosurg, Brighton BN2 5BE, E Sussex, England
[4] Royal Coll Surgeons Ireland, Dublin D02 YN77, Ireland
[5] Beaumont Hosp, Dept Neurosurg, Dublin D09 V2N0, Ireland
[6] Univ Brighton, Sch Appl Sci, Ctr Stress & Age Related Dis, Brighton BN2 4GJ, E Sussex, England
关键词
glioblastoma; extracellular vesicles; liquid biopsy; CENTRAL-NERVOUS-SYSTEM; FC BINDING-PROTEIN; PROGNOSTIC-SIGNIFICANCE; LIQUID BIOPSIES; CELLS; ALPHA-1-ANTITRYPSIN; CLASSIFICATION; EXPRESSION; EXOSOMES; MICROVESICLES;
D O I
10.3390/biomedicines10010125
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glioblastoma (GB) is an aggressive type of tumour for which therapeutic options and biomarkers are limited. GB diagnosis mostly relies on symptomatic presentation of the tumour and, in turn, brain imaging and invasive biopsy that can delay its diagnosis. Description of easily accessible and effective biomarkers present in biofluids would thus prove invaluable in GB diagnosis. Extracellular vesicles (EVs) derived from both GB and stromal cells are essential to intercellular crosstalk in the tumour bulk, and circulating EVs have been described as a potential reservoir of GB biomarkers. Therefore, EV-based liquid biopsies have been suggested as a promising tool for GB diagnosis and follow up. To identify GB specific proteins, sEVs were isolated from plasma samples of GB patients as well as healthy volunteers using differential ultracentrifugation, and their content was characterised through mass spectrometry. Our data indicate the presence of an inflammatory biomarker signature comprising members of the complement and regulators of inflammation and coagulation including VWF, FCGBP, C3, PROS1, and SERPINA1. Overall, this study is a step forward in the development of a non-invasive liquid biopsy approach for the identification of valuable biomarkers that could significantly improve GB diagnosis and, consequently, patients' prognosis and quality of life.
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页数:15
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