Pitt Shield

Focused ultrasound for safe and effective release of brain tumor biomarkers into the peripheral circulation.

Authors: Zhu L, Nazeri A, Pacia CP, Yue Y, Chen H

The development of noninvasive approaches for brain tumor diagnosis and monitoring continues to be a major medical challenge. Although blood-based liquid biopsy has received considerable attention in various cancers, limited progress has been made for brain tumors, at least partly due to the hindrance of tumor biomarker release into the peripheral circulation by the blood-brain barrier. Focused ultrasound (FUS) combined with microbubbles induced BBB disruption has been established as a promising technique for noninvasive and localized brain drug delivery. Building on this established technique, we propose to develop FUS-enabled liquid biopsy technique (FUS-LBx) to enhance the release of brain tumor biomarkers (e.g., DNA, RNA, and proteins) into the circulation. The objective of this study was to demonstrate that FUS-LBx could sufficiently increase plasma levels of brain tumor biomarkers without causing hemorrhage in the brain. Mice with orthotopic implantation of enhanced green fluorescent protein (eGFP)-transfected murine glioma cells were treated using magnetic resonance (MR)-guided FUS system in the presence of systemically injected microbubbles at three peak negative pressure levels (0.59, 1.29, and 1.58 MPa). Plasma eGFP mRNA levels were quantified with the quantitative polymerase chain reaction (qPCR). Contrast-enhanced MR images were acquired before and after the FUS sonication. FUS at 0.59 MPa resulted in an increased plasma eGFP mRNA level, comparable to those at higher acoustic pressures (1.29 MPa and 1.58 MPa). Microhemorrhage density associated with FUS at 0.59 MPa was significantly lower than that at higher acoustic pressures and not significantly different from the control group. MRI analysis revealed that post-sonication intratumoral and peritumoral hyperenhancement had strong correlations with the level of FUS-induced biomarker release and the extent of hemorrhage. This study suggests that FUS-LBx could be a safe and effective brain-tumor biomarker release technique, and MRI could be used to develop image-guided FUS-LBx.

Introduction

Purpose Sonobiopsy
Study Objective To demonstrate that focused ultrasound-enabled liquid biopsy (FUS-LBx) can increase plasma levels of brain tumor biomarkers without causing hemorrhage in the brain.
Animal model / Human subject mouse, NIH Swiss, 6–8 weeks, female
Disease model glioma
MRI or image guidance method MR-guided (clinical MR-guided FUS system, Sonalleve V2 integrated with a 1.5T MRI and small-animal coil)
Targeted brain region(s) Tumor Site
Target coordinates AP: 2 mm posterior to bregma; ML: 1.5 mm lateral to bregma; DV: not specified

Outcomes and Safety

Summary of Outcomes MR-guided FUS-enabled liquid biopsy (Sonobiopsy) significantly increased plasma tumor-derived mRNA levels in a mouse glioma model.
Duration of biological effect not reported
Safety-related matter Low-pressure sonication (0.59 MPa) effectively released biomarkers without significant microhemorrhage or off-target brain damage.

Brain Region

Ultrasound Parameters

Ultrasound instrument Sonalleve V2 MR-guided FUS system
FUS Frequency 1.44 MHz
FUS Intensity not reported
FUS Pressure 0.59 MPa, 1.29 MPa, 1.58 MPa
FUS Mode pulsed
Pulse duration 10 ms
Duration of a single FUS session 4 min
Focal Characteristics Focal depth: 12.10 mm; Focal length: none; Aperture size: none
Treatment frequency single

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