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聚焦超声用于安全有效地将脑肿瘤生物标志物释放到外周循环中。

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

机构信息

Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, Missouri, United States of America.

Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri, United States of America.

出版信息

PLoS One. 2020 Jun 3;15(6):e0234182. doi: 10.1371/journal.pone.0234182. eCollection 2020.

Abstract

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.

摘要

非侵入性脑肿瘤诊断和监测方法的发展仍然是一个主要的医学挑战。尽管基于血液的液体活检在各种癌症中受到了相当多的关注,但在脑肿瘤方面进展有限,这至少部分是由于血脑屏障阻碍了肿瘤生物标志物释放到外周循环。聚焦超声(FUS)联合微泡诱导的血脑屏障破坏已被确立为一种有前途的非侵入性和局部脑药物递送技术。在此基础上,我们提出开发 FUS 增强的液体活检技术(FUS-LBx),以增强脑肿瘤生物标志物(如 DNA、RNA 和蛋白质)释放到循环系统中。本研究的目的是证明 FUS-LBx 可以在不引起脑内出血的情况下,充分增加脑肿瘤生物标志物的血浆水平。用携带增强型绿色荧光蛋白(eGFP)的转染鼠胶质瘤细胞进行原位移植的小鼠,在系统注射微泡的情况下,使用磁共振(MR)引导的 FUS 系统,在三个峰值负压水平(0.59、1.29 和 1.58 MPa)下进行治疗。用定量聚合酶链反应(qPCR)定量检测血浆 eGFP mRNA 水平。在 FUS 超声处理前后采集对比增强磁共振图像。FUS 在 0.59 MPa 时导致血浆 eGFP mRNA 水平增加,与较高声压(1.29 MPa 和 1.58 MPa)相当。与 0.59 MPa 时的 FUS 相关的微出血密度明显低于较高声压,与对照组无显著差异。MRI 分析表明,超声处理后肿瘤内和肿瘤周围的高增强与 FUS 诱导的生物标志物释放水平和出血程度有很强的相关性。本研究表明,FUS-LBx 可能是一种安全有效的脑肿瘤生物标志物释放技术,MRI 可用于开发图像引导的 FUS-LBx。

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