Department of Biomedical Engineering, Washington University in St. Louis, Saint Louis, MO, 63130, USA.
Department of Mechanical Engineering and Materials Science, Washington University in St. Louis, Saint Louis, MO, 63130, USA.
Sci Rep. 2018 Apr 26;8(1):6553. doi: 10.1038/s41598-018-24516-7.
Although blood-based liquid biopsies have emerged as a promising non-invasive method to detect biomarkers in various cancers, limited progress has been made for brain tumors. One major obstacle is the blood-brain barrier (BBB), which hinders efficient passage of tumor biomarkers into the peripheral circulation. The objective of this study was to determine whether FUS in combination with microbubbles can enhance the release of biomarkers from the brain tumor to the blood circulation. Two glioblastoma tumor models (U87 and GL261), developed by intracranial injection of respective enhanced green fluorescent protein (eGFP)-transduced glioblastoma cells, were treated by FUS in the presence of systemically injected microbubbles. Effect of FUS on plasma eGFP mRNA levels was determined using quantitative polymerase chain reaction. eGFP mRNA were only detectable in the FUS-treated U87 mice and undetectable in the untreated U87 mice (maximum cycle number set to 40). This finding was replicated in GL261 mice across three different acoustic pressures. The circulating levels of eGFP mRNA were 1,500-4,800 fold higher in the FUS-treated GL261 mice than that of the untreated mice for the three acoustic pressures. This study demonstrated the feasibility of FUS-enabled brain tumor liquid biopsies in two different murine glioma models across different acoustic pressures.
虽然基于血液的液体活检已成为一种很有前途的非侵入性方法,可用于检测各种癌症中的生物标志物,但脑肿瘤的进展有限。一个主要障碍是血脑屏障(BBB),它阻碍了肿瘤标志物有效地进入外周循环。本研究的目的是确定 FUS 联合微泡是否可以增强脑肿瘤标志物向血液循环的释放。通过颅内注射各自携带增强型绿色荧光蛋白(eGFP)的神经胶质瘤细胞,建立了两个神经胶质瘤肿瘤模型(U87 和 GL261),并用系统注射的微泡进行 FUS 处理。使用定量聚合酶链反应(PCR)确定 FUS 对血浆 eGFP mRNA 水平的影响。在用 FUS 处理的 U87 小鼠中可以检测到 eGFP mRNA,但在未处理的 U87 小鼠中无法检测到(最大循环数设置为 40)。在三个不同声压下的 GL261 小鼠中复制了这一发现。在用 FUS 处理的 GL261 小鼠中,循环中的 eGFP mRNA 水平比未处理的小鼠高 1500-4800 倍,这三个声压均如此。这项研究证明了 FUS 使脑肿瘤液体活检在两种不同的小鼠神经胶质瘤模型中具有可行性,而且跨越了不同的声压。