Jiang Yanyan, Allen Danny, Kersemans Veerle, Devery Aoife M, Bokobza Sivan M, Smart Sean, Ryan Anderson J
CRUK & MRC Oxford Institute for Radiation Oncology, Department of Oncology, University of Oxford, Roosevelt Drive, Oxford OX3 7DQ, United Kingdom.
CRUK & MRC Oxford Institute for Radiation Oncology, Department of Oncology, University of Oxford, Roosevelt Drive, Oxford OX3 7DQ, United Kingdom.
Lung Cancer. 2015 Nov;90(2):191-8. doi: 10.1016/j.lungcan.2015.08.009. Epub 2015 Aug 20.
Tumours can be categorised based on their stromal architecture into tumour vessel and stromal vessel phenotypes, and the phenotypes have been suggested to define tumour response to chronic treatment with a VEGFR2 antibody. However, it is unclear whether the vascular phenotypes of tumours associate with acute vascular response to VEGFR tyrosine kinase inhibitors (TKI), or whether the early changes in vascular function are associated with subsequent changes in tumour size. This study was sought to address these questions by using xenograft models of human non-small cell lung cancer (NSCLC) representing stromal vessel phenotype (Calu-3) and tumour vessel phenotype (Calu-6), respectively.
For dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI), nude mice bearing established Calu-3 or Calu-6 xenografts were treated with a potent pan-VEGFR TKI, cediranib (6 mg/kg), at 0 h and 22 h. DCE-MRI was performed 2h before the first dose and 2h after the second dose of cediranib to examine acute changes in tumour vessel perfusion. Tumours were harvested for hypoxia detection by CA9 immunohistochemistry. For tumour growth study, mice carrying established Calu-3 or Calu-6 tumours were treated with cediranib once daily for 5 days.
Twenty-four hours after cediranib administration, the perfusion of Calu-3 tumours was markedly reduced, with a significant increase in hypoxia. In contrast, neither perfusion nor hypoxia was significantly affected in Calu-6 tumours. Tumour regressions were induced in Calu-3 xenografts, but not in Calu-6 xenografts, although there was a trend towards tumour growth inhibition after 5 days of cediranib treatment.
These findings suggest that tumour stromal architecture may associate with acute tumour vascular response to VEGFR TKI, and this acute tumour vascular response may be a promising early predictive marker of response to VEGFR TKI in NSCLC.
肿瘤可根据其基质结构分为肿瘤血管型和基质血管型,有人提出这些表型可用于定义肿瘤对VEGFR2抗体慢性治疗的反应。然而,尚不清楚肿瘤的血管表型是否与对VEGFR酪氨酸激酶抑制剂(TKI)的急性血管反应相关,或者血管功能的早期变化是否与肿瘤大小的后续变化相关。本研究旨在通过使用分别代表基质血管型(Calu-3)和肿瘤血管型(Calu-6)的人非小细胞肺癌(NSCLC)异种移植模型来解决这些问题。
对于动态对比增强磁共振成像(DCE-MRI),在0小时和22小时用强效泛VEGFR TKI西地尼布(6mg/kg)治疗携带已建立的Calu-3或Calu-6异种移植瘤的裸鼠。在首次给药西地尼布前2小时和第二次给药后2小时进行DCE-MRI,以检查肿瘤血管灌注的急性变化。通过CA9免疫组织化学收获肿瘤用于缺氧检测。对于肿瘤生长研究,对携带已建立的Calu-3或Calu-6肿瘤的小鼠每天用西地尼布治疗一次,持续5天。
给予西地尼布24小时后,Calu-3肿瘤的灌注明显降低,缺氧显著增加。相比之下,Calu-6肿瘤的灌注和缺氧均未受到显著影响。Calu-3异种移植瘤诱导了肿瘤消退,但Calu-6异种移植瘤未出现,尽管西地尼布治疗5天后有肿瘤生长抑制趋势。
这些发现表明肿瘤基质结构可能与对VEGFR TKI的急性肿瘤血管反应相关,并且这种急性肿瘤血管反应可能是NSCLC中对VEGFR TKI反应的有前景的早期预测标志物。