Klotz Laura V, Clevert Dirk-Andre, Scheckinger Siiri, Strieth Sebastian, Eichhorn Martin E
Clinic of General, Visceral, Transplantation, Vascular and Thoracic Surgery, Ludwig-Maximilians-University of Munich, Munich, Germany Walter-Brendel-Centre of Experimental Medicine, University of Munich, Munich, Germany
Department of Clinical Radiology, University of Munich, Munich, Germany.
Anticancer Res. 2015 May;35(5):2571-6.
BACKGROUND/AIM: Anti-angiogenic treatment is a promising strategy for cancer therapy and is currently evaluated in clinical trials. The aim of the present study was to further investigate the effects of an anti-angiogenic therapy, inhibiting vascular endothelial growth factor (VEGF) and endothelial growth factor (EGF) using a tyrosine kinase inhibitor for blocking tumor angiogenesis and tumor progression in vivo.
Experiments were performed using C57/Bl6 mice (25 ± 5 g of body weight (b.w.)) implanted with subcutaneous Lewis lung carcinoma (LLC-1). From day 7 till 21 after tumor cell implantation, animals (n=7 per group) were treated by monotherapy using ZD6474 (50 mg/kg b.w. per os (p.o.)) daily. A control group received only the solvent polysorbate 80. Using contrast enhanced ultrasound (CE-US) parameters of intra-tumoral microcirculation animals were examined 24 h after the last application of ZD6474. Moreover, subcutaneous tumor growth was measured over the whole therapy period. Finally, histological analyses were performed to analyze the functional vessel density in the tumor tissue.
ZD6474 reduced tumor growth of LLC-1 in C57/Bl6 mice significantly. A significant difference of maximal signal intensity (ΔSImax) and area below the intensity time curve (AUC) after antiangiogenic therapy was recorded in the tumor center by CE-US. Vessel density after hematoxyline and eosin, as well as CD31, staining showed no significant difference in both groups.
Anti-angiogenic effects can be quantitatively demonstrated using CE-US imaging, which represents the spreading of efficient vessels in the tumor tissue, especially in the tumor center.
背景/目的:抗血管生成治疗是一种很有前景的癌症治疗策略,目前正在临床试验中进行评估。本研究的目的是进一步研究一种抗血管生成疗法的效果,该疗法使用酪氨酸激酶抑制剂抑制血管内皮生长因子(VEGF)和内皮生长因子(EGF),以阻断体内肿瘤血管生成和肿瘤进展。
实验使用植入皮下Lewis肺癌(LLC-1)的C57/Bl6小鼠(体重25±5克)进行。在肿瘤细胞植入后第7天至21天,动物(每组n = 7)每天口服ZD6474(50毫克/千克体重)进行单药治疗。对照组仅接受溶剂聚山梨酯80。在最后一次应用ZD6474后24小时,使用对比增强超声(CE-US)参数检查肿瘤内微循环的动物。此外,在整个治疗期间测量皮下肿瘤生长。最后,进行组织学分析以分析肿瘤组织中的功能性血管密度。
ZD6474显著降低了C57/Bl6小鼠中LLC-1的肿瘤生长。通过CE-US在肿瘤中心记录到抗血管生成治疗后最大信号强度(ΔSImax)和强度时间曲线下面积(AUC)的显著差异。苏木精和伊红染色以及CD31染色后的血管密度在两组中均无显著差异。
使用CE-US成像可以定量证明抗血管生成作用,这代表了肿瘤组织中有效血管的扩散,尤其是在肿瘤中心。