Goto Hisatsugu, Yano Seiji, Zhang Helong, Matsumori Yuka, Ogawa Hirohisa, Blakey David C, Sone Saburo
Department of Internal Medicine and Molecular Therapeutics, Course of Medical Oncology, The University of Tokushima School of Medicine, Tokushima 770-8503, Japan.
Cancer Res. 2002 Jul 1;62(13):3711-5.
ZD6126 (ANG453) is a novel vascular targeting agent that selectively disrupts the cytoskeleton of endothelial cells in tumor. In mouse s.c. xenograft models, ZD6126 was found to induce selective occlusion of tumor blood vessels, cessation of tumor blood flow, and death of tumor cells because of the starvation of oxygen and nutrition. Here, we investigated whether ZD6126 inhibited the metastatic formation of human non-small cell lung cancer cells. PC14PE6 (adenocarcinoma) and H226 (squamous cell carcinoma) cells were injected into the tail vein of nude mice, and lung metastases were estimated. ZD6126 treatment involved either a single dose on 24 h before killing or daily doses from day 14 until the end of the experiment. Single treatment with i.p. injection of 200 mg/kg ZD6126 caused bleeding and necrotic changes in the tumor by 24 h. Histological analysis revealed that apoptotic tumor cells were markedly increased in the ZD6126-treated group. Moreover, ZD6126 induced the apoptosis of CD31-positive vascular endothelial cells in tumors but not in the normal lung parenchyma. When mice were treated daily with 100 mg/kg ZD6126 from day 14 until the end of the experiment, the lung weight was significantly less in the ZD6126-treated group than that of the control group, despite no difference in the number of metastatic nodules. These data suggest that ZD6126 could demonstrate its antitumor activity against both already established and early phase of lung cancer metastasis by causing the selective apoptosis of tumor endothelial cells and destruction of the tumor vasculature.
ZD6126(ANG453)是一种新型血管靶向药物,可选择性破坏肿瘤内皮细胞的细胞骨架。在小鼠皮下异种移植模型中,发现ZD6126可诱导肿瘤血管选择性闭塞、肿瘤血流停止以及肿瘤细胞因缺氧和营养饥饿而死亡。在此,我们研究了ZD6126是否能抑制人非小细胞肺癌细胞的转移形成。将PC14PE6(腺癌)和H226(鳞状细胞癌)细胞注入裸鼠尾静脉,并评估肺转移情况。ZD6126治疗包括在处死前24小时单次给药或从第14天开始直至实验结束每日给药。腹腔注射200mg/kg ZD6126单次治疗在24小时内导致肿瘤出现出血和坏死变化。组织学分析显示,ZD6126治疗组凋亡的肿瘤细胞明显增多。此外,ZD6126诱导肿瘤中CD31阳性血管内皮细胞凋亡,但不诱导正常肺实质细胞凋亡。当从第14天开始直至实验结束每天用100mg/kg ZD6126治疗小鼠时,尽管转移结节数量无差异,但ZD6126治疗组的肺重量明显低于对照组。这些数据表明,ZD6126可通过诱导肿瘤内皮细胞选择性凋亡和破坏肿瘤脉管系统,对已形成的肺癌转移以及肺癌转移早期阶段发挥抗肿瘤活性。