Yuasa Takeshi, Nogawa Masaki, Kimura Shinya, Yokota Asumi, Sato Kiyoshi, Segawa Hidekazu, Kuroda Junya, Maekawa Taira
Department of Transfusion Medicine and Cell Therapy, Kyoto University Hospital, 54 Kawahara-cho Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.
Clin Cancer Res. 2005 Jan 15;11(2 Pt 1):853-9.
Minodronic acid (YM529) is a third-generation nitrogen-containing bisphosphonate. Here, we have investigated the therapeutic efficacy of YM529 against renal cell cancer (RCC) alone or in combination with IFN both in vitro and in vivo.
One murine and eight human RCC cell lines were used for the in vitro studies and were subjected to a modified 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and Western blotting. Luciferase-labeled murine RCC cells (RENCA(Luc)) were transplanted into the s.c. tissue or the renal subcapsule of syngeneic BALB/c mice. These mice were treated with YM529 and/or murine IFN and the growth of the cancer cells was monitored by an in vivo imaging system.
YM529 inhibited the growth of RCC cells in a dose- and time-dependent manner and enhanced the growth inhibitory potential of IFN in vitro. In the in vivo mouse models, YM529 did not markedly inhibit the RCC cell growth on its own but it augmented the anticancer effect of IFN (P < 0.05). The YM529-treated mice (with or without IFN) did not alter the gamma/delta T-lymphocyte numbers. The various treatment regimens were also not associated with any adverse effects. However, YM529 combined with IFN reduced the serum vascular endothelial growth factor levels.
Our study suggests that YM529 may be a potent anticancer agent for RCC. The efficacy and safety of IFN plus YM529 as a therapy for RCC should be verified by early-phase clinical trials.
米诺膦酸(YM529)是第三代含氮双膦酸盐。在此,我们研究了YM529单独或与干扰素联合对肾细胞癌(RCC)的体内外治疗效果。
使用一种小鼠和八种人RCC细胞系进行体外研究,并进行改良的3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐检测和蛋白质印迹分析。将荧光素酶标记的小鼠RCC细胞(RENCA(Luc))移植到同基因BALB/c小鼠的皮下组织或肾被膜下。用YM529和/或小鼠干扰素治疗这些小鼠,并通过体内成像系统监测癌细胞的生长。
YM529以剂量和时间依赖性方式抑制RCC细胞的生长,并在体外增强了干扰素的生长抑制潜力。在体内小鼠模型中,YM529单独使用时并未明显抑制RCC细胞生长,但增强了干扰素的抗癌效果(P < 0.05)。接受YM529治疗的小鼠(无论是否使用干扰素)γ/δ T淋巴细胞数量未改变。各种治疗方案也未产生任何不良反应。然而,YM529与干扰素联合使用可降低血清血管内皮生长因子水平。
我们的研究表明YM529可能是一种有效的RCC抗癌药物。干扰素加YM529作为RCC治疗方法的疗效和安全性应通过早期临床试验进行验证。