Zhang Cathy C, Yan Zhengming, Giddabasappa Anand, Lappin Patrick B, Painter Cory L, Zhang Qin, Li Gang, Goodman James, Simmons Brett, Pascual Bernadette, Lee Joseph, Levkoff Ted, Nichols Tim, Xie Zhiyong
Oncology Research Unit, Pfizer Global Research and Development, La Jolla, California.
Cancer Med. 2014 Jun;3(3):462-71. doi: 10.1002/cam4.215. Epub 2014 Feb 27.
Noninvasive imaging has been widely applied for monitoring antiangiogenesis therapy in cancer drug discovery. In this report, we used different imaging modalities including high-frequency ultrasound (HFUS), dynamic contrast enhanced-MR (DCE-MR), and fluorescence molecular tomography (FMT) imaging systems to monitor the changes in the tumor vascular properties after treatment with γ-secretase inhibitor PF-03084014. Sunitinib was tested in parallel for comparison. In the MDA-MB-231Luc model, we demonstrated that antiangiogenesis was one of the contributing mechanisms for the therapeutic effect of PF-03084014. By immunohistochemistry and FITC-lectin perfusion assays, we showed that the vascular defects upon treatment with PF-03084014 were associated with Notch pathway modulation, evidenced by a decrease in the HES1 protein and by the changes in VEGFR2 and HIF1α levels, which indicates down-stream effects. Using a 3D power Doppler scanning method, ultrasound imaging showed that the% vascularity in the MDA-MB-231Luc tumor decreased significantly at 4 and 7 days after the treatment with PF-03084014. A decrease in the tumor vessel function was also observed through contrast-enhanced ultrasound imaging with microbubble injection. These findings were consistent with the PF-03084014-induced functional vessel changes measured by suppressing the K(trans) values using DCE-MRI. In contrast, the FMT imaging with the AngioSence 680EX failed to detect any treatment-associated tumor vascular changes. Sunitinib demonstrated an outcome similar to PF-03084014 in the tested imaging modalities. In summary, ultrasound and DCE-MR imaging successfully provided longitudinal measurement of the phenotypic and functional changes in tumor vasculature after treatment with PF-03084014 and sunitinib.
在癌症药物研发中,非侵入性成像已广泛应用于监测抗血管生成治疗。在本报告中,我们使用了不同的成像方式,包括高频超声(HFUS)、动态对比增强磁共振(DCE-MR)和荧光分子断层扫描(FMT)成像系统,来监测γ-分泌酶抑制剂PF-03084014治疗后肿瘤血管特性的变化。同时对舒尼替尼进行了平行测试以作比较。在MDA-MB-231Luc模型中,我们证明抗血管生成是PF-03084014治疗效果的作用机制之一。通过免疫组织化学和FITC-凝集素灌注分析,我们表明PF-03084014治疗后的血管缺陷与Notch通路调节有关,这通过HES1蛋白的减少以及VEGFR2和HIF1α水平的变化得以证明,这表明了下游效应。使用三维能量多普勒扫描方法,超声成像显示PF-03084014治疗后4天和7天,MDA-MB-231Luc肿瘤中的血管百分比显著下降。通过注射微泡的对比增强超声成像也观察到肿瘤血管功能的下降。这些发现与通过DCE-MRI抑制K(trans)值测量的PF-03084014诱导的功能性血管变化一致。相比之下,使用AngioSence 680EX的FMT成像未能检测到任何与治疗相关的肿瘤血管变化。在测试的成像方式中,舒尼替尼显示出与PF-03084014相似的结果。总之,超声和DCE-MR成像成功地提供了PF-03084014和舒尼替尼治疗后肿瘤血管系统表型和功能变化的纵向测量。