Abstract

Extracellular vesicles (EVs) are small, membrane-bound particles released by all cells that have emerged as an attractive biomarker platform. We study the utility of a dielectrophoretic (DEP) micro-chip device for isolation and characterization of EVs derived from plasma specimens from patients with brain tumors. EVs were isolated by DEP chip and subjected to on-chip immunofluorescence (IF) staining to determine the concentration of glial fibrillary acidic protein (GFAP) and Tau. EVs were analyzed from the plasma samples isolated from independent patient cohorts. Glioblastoma cell lines secrete EVs enriched for GFAP and Tau. These EVs can be efficiently isolated using the DEP platform. Application of DEP to clinical plasma samples afforded discrimination of plasma derived from brain tumor patients relative to those derived from patients without history of brain cancer. Sixty-five percent (11/17) of brain tumor patients showed higher EV-GFAP than the maximum observed in controls. Ninety-four percent (16/17) of tumor patients showed higher EV-Tau than the maximum observed in controls. These discrimination thresholds were applied to plasma isolated from a second, independent cohort of 15 glioblastoma patients and 8 controls. For EV-GFAP, we observed 93% sensitivity, 38% specificity, 74% PPV, 75% NPV, and AUC of 0.65; for EV-Tau, we found 67% sensitivity, 75% specificity 83% PPV, 55% NPV, and AUC of 0.71 for glioblastoma diagnosis. This proof-of-principle study provides support for DEP-IF of plasma EVs for diagnosis of glioblastoma.

Highlights

  • We tested this platform to detect Extracellular vesicles (EVs)-contained glial fibrillary acidic protein (GFAP) and Tau in patients with and without a diagnosis of glioblastoma

  • We hypothesized that GFAP and Tau had potential as biomarkers for glioblastoma because 1) glioblastoma growth inevitably damages nearby astrocytes and neurons, releasing free GFAP and Tau into the surrounding tissues and fluid compartments[25], and 2) GFAP and Tau are highly expressed in glioblastoma and may be enriched in their EVs26,27

  • These results suggest that brain tumor cells release EVs containing GFAP and Tau and suggest that EV GFAP and Tau have potential as brain tumor biomarkers

Read more

Summary

Introduction

We tested this platform to detect EV-contained glial fibrillary acidic protein (GFAP) and Tau in patients with and without a diagnosis of glioblastoma. GFAP encodes an intermediate filament protein that is highly abundant in astrocytes[18], and Tau is a microtubule-stabilizing protein that is highly expressed in neurons[19] Both proteins closely associate with cellular membranes and can be detected in EVs20–22. EVs isolated from plasma of brain tumor patients should contain higher concentrations of GFAP and Tau compared to samples from normal patients. Our findings support this hypothesis and provide proof-of-principle data for DEP microarray and on-chip immunofluorescence analysis of EV-contained GFAP and Tau as a potential glioblastoma detection platform

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call