Raes Florian, Sobilo Julien, Le Mée Marilyne, Rétif Stéphanie, Natkunarajah Sharuja, Lerondel Stéphanie, Le Pape Alain
PHENOMIN-TAAM-UPS44, CIPA (Centre d'Imagerie du Petit Animal), CNRS Orléans, France.
INSERM U1100, CEPR, University of Tours, France.
PLoS One. 2016 Apr 12;11(4):e0153532. doi: 10.1371/journal.pone.0153532. eCollection 2016.
We have developed a relevant preclinical model associated with a specific imaging protocol dedicated to onco-pharmacology studies in mice.
We optimized both the animal model and an ultrasound imaging procedure to follow up longitudinally the lung tumor growth in mice. Moreover we proposed to measure by photoacoustic imaging the intratumoral hypoxia, which is a crucial parameter responsible for resistance to therapies. Finally, we compared ultrasound data to x-ray micro computed tomography and volumetric measurements to validate the relevance of this approach on the NCI-H460 human orthotopic lung tumor.
This study demonstrates the ability of ultrasound imaging to detect and monitor the in vivo orthotopic lung tumor growth by high resolution ultrasound imaging. This approach enabled us to characterize key biological parameters such as oxygenation, perfusion status and vascularization of tumors.
Such an experimental approach has never been reported previously and it would provide a nonradiative tool for assessment of anticancer therapeutic efficacy in mice. Considering the absence of ultrasound propagation through the lung parenchyma, this strategy requires the implantation of tumors strictly located in the superficial posterior part of the lung.
我们开发了一种与特定成像方案相关的临床前模型,该方案专门用于小鼠的肿瘤药理学研究。
我们优化了动物模型和超声成像程序,以纵向跟踪小鼠肺部肿瘤的生长。此外,我们提议通过光声成像测量肿瘤内缺氧情况,这是导致治疗抗性的关键参数。最后,我们将超声数据与X射线微型计算机断层扫描和体积测量进行比较,以验证该方法对NCI-H460人原位肺肿瘤的相关性。
本研究证明了超声成像通过高分辨率超声成像检测和监测体内原位肺肿瘤生长的能力。这种方法使我们能够表征关键的生物学参数,如肿瘤的氧合、灌注状态和血管生成。
这种实验方法以前从未有过报道,它将为评估小鼠抗癌治疗效果提供一种无辐射工具。考虑到超声无法穿过肺实质传播,该策略要求植入的肿瘤严格位于肺的浅表后部。