Department of Radiology, Thomas Jefferson University, Philadelphia, PA, USA; School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA; College of Applied Medical Sciences King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia; King Abdullah International Medical Research Center, Jeddah, Saudi Arabia.
Department of Radiology, Thomas Jefferson University, Philadelphia, PA, USA; School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA.
Ultrasound Med Biol. 2024 Sep;50(9):1387-1394. doi: 10.1016/j.ultrasmedbio.2024.05.015. Epub 2024 Jun 13.
Both microbubble ultrasound contrast agents and acoustic phase change droplets (APCD) have been explored in hepatocellular carcinoma (HCC). This work aimed to evaluate changes to the HCC microenvironment following either microbubble or APCD destruction in a syngeneic pre-clinical model.
Mouse RIL-175 HCC tumors were grown in the right flank of 64 immunocompetent mice. Pre-treatment, photoacoustic volumetric tumor oxygenation, and power Doppler measurements were obtained using a Vevo 3100 system (VisualSonics, Toronto, Canada). The experimental groups received a 0.1 mL bolus injection of either Definity ultrasound contrast agent (Lantheus Medical Imaging) or APCD fabricated by condensing Definity. Following injection, ultrasound destruction was performed using flash-replenishment sequences on a Sequoia with a 10L4 probe (Siemens) for the duration of enhancement. Tumor oxygenation and power Doppler measurements were then repeated immediately post-ultrasound treatment. Twenty-four hours post-treatment, animals were euthanized, and tumors were harvested and stained for CD31, Cleaved Caspase 3 and CD45.
Imaging biomarkers demonstrated a significant reduction in percent vascularity following either microbubble or APCD destruction in the tumor microenvironment ( p < 0.022) but no significant changes in tumor oxygenation (p = 0.12). Similarly, immunohistochemistry data demonstrated a significant decrease in CD31 expression (p < 0.042) and an increase in apoptosis (p < 0.014) in tumors treated with destroyed microbubbles or APCD relative to controls. Finally, a significant increase in CD45 expression was observed in tumors treated with APCD (p = 0.046), indicating an increase in tumor immune response.
Ultrasound-triggered destruction of both microbubbles and APCD reduces vascularity, increases apoptosis, and may also increase immune response in this HCC model.
微泡超声对比剂和声学相变法液滴(APCD)已在肝细胞癌(HCC)中进行了探索。本研究旨在评估在同种异体临床前模型中,微泡或 APCD 破坏后 HCC 微环境的变化。
将小鼠 RIL-175 HCC 肿瘤种植在 64 只免疫功能正常的小鼠的右侧肋部。使用 Vevo 3100 系统(加拿大多伦多的 VisualSonics)获得治疗前的光声体积肿瘤氧合和功率多普勒测量值。实验组接受 0.1 mL 推注 Definity 超声对比剂(Lantheus Medical Imaging)或通过冷凝 Definity 制成的 APCD。注射后,使用 Sequoia 上的 Flash-Restock 序列进行超声破坏,持续增强时间为 10L4 探头(西门子)。超声治疗后立即重复肿瘤氧合和功率多普勒测量值。治疗后 24 小时,处死动物,采集肿瘤并进行 CD31、Cleaved Caspase 3 和 CD45 染色。
成像生物标志物显示,微泡或 APCD 破坏后肿瘤微环境中的血管百分比显著降低(p < 0.022),但肿瘤氧合无显著变化(p = 0.12)。同样,免疫组化数据表明,与对照组相比,用破坏的微泡或 APCD 处理的肿瘤中 CD31 表达显著降低(p < 0.042),凋亡增加(p < 0.014)。最后,在 APCD 处理的肿瘤中观察到 CD45 表达显著增加(p = 0.046),表明肿瘤免疫反应增加。
超声触发的微泡和 APCD 破坏可降低血管生成,增加细胞凋亡,并可能增加该 HCC 模型中的免疫反应。