Mori S, Ueda T, Kuratsu S, Hosono N, Izawa K, Uchida A
Department of Orthopedic Surgery, Center for Adult Diseases, Osaka, Japan.
Int J Cancer. 1995 Mar 29;61(1):148-52. doi: 10.1002/ijc.2910610125.
We treated a murine osteosarcoma cell line, LM8, which preferentially metastasizes to the lungs, with a new angiogenesis inhibitor, TNP-470, to evaluate the efficacy of this compound in the suppression of pulmonary metastasis of osteosarcoma. In an in vivo experiment, tumor cells were inoculated i.v. into C3H mice, and TNP-470 or vehicle alone (control group) was administered s.c. every day for 3 weeks. In the TNP-470-treated groups, both the number of pulmonary metastatic nodules and the lung wet weight were significantly reduced in a dose-dependent manner. Similarly, vascular density in the metastatic tumors estimated by immunohistochemical staining with anti-von-Willebrand factor antibody as an endothelial marker were significantly reduced. No severe side-effects were found. In an in vitro experiment, viable tumor cells were counted after 3 days' treatment with TNP-470. The 50% inhibitory concentration was 0.6 ng/ml for LM8, which was more sensitive than other tumor cells previously reported. Our results show that TNP-470 suppresses the pulmonary metastasis of LM8 and suggest that both its anti-angiogenic activity and cytostatic activity towards LM8 are responsible for the antitumor effect.
我们用一种新型血管生成抑制剂TNP - 470处理一种优先转移至肺部的小鼠骨肉瘤细胞系LM8,以评估该化合物在抑制骨肉瘤肺转移方面的疗效。在一项体内实验中,将肿瘤细胞经静脉注射接种到C3H小鼠体内,每天皮下注射TNP - 470或单独的赋形剂(对照组),持续3周。在TNP - 470处理组中,肺转移结节数量和肺湿重均以剂量依赖方式显著减少。同样,以抗血管性血友病因子抗体作为内皮标志物进行免疫组织化学染色评估的转移瘤血管密度也显著降低。未发现严重副作用。在一项体外实验中,用TNP - 470处理3天后对存活肿瘤细胞进行计数。LM8的50%抑制浓度为0.6 ng/ml,其比先前报道的其他肿瘤细胞更敏感。我们的结果表明,TNP - 470可抑制LM8的肺转移,并提示其抗血管生成活性和对LM8的细胞生长抑制活性均对抗肿瘤作用有贡献。