Wood P J, Hirst D G
Department of Radiation Oncology, Stanford University School of Medicine, CA 94305.
Br J Cancer. 1988 Dec;58(6):742-5. doi: 10.1038/bjc.1988.301.
The effect of the calcium antagonists, cinnarizine and flunarizine on the radiation sensitivity of two murine tumours, RIF-1 and SCCVII/St was investigated. Initial experiments giving the compounds at 50 mg kg-1 i.p. indicated that cinnarizine had no effect on cell survival after 20 Gy of X-rays in the RIF-1 sarcoma and only a small effect in the SCCVII/St carcinoma. However, flunarizine produced a small radiosensitisation in the RIF-1 tumour and a substantial sensitisation in the SCCVII/St tumour. Subsequent experiments in the SCCVII/St tumour indicated that the optimal radiosensitising dose of flunarizine was approximately 5 mg kg-1, although some sensitisation was apparent throughout the range of 0.05-500 mg kg-1. Flunarizine produced a parallel shift in the X-ray dose response curve, equivalent to a 5-fold reduction in hypoxic fraction. In a normal tissue study, 5 mg kg-1 flunarizine did not enhance the reduction in white cell counts produced by X-ray doses of 2-8 Gy. These data suggest that flunarizine may have some potential use as a radiosensitiser.
研究了钙拮抗剂桂利嗪和氟桂利嗪对两种小鼠肿瘤RIF-1和SCCVII/St辐射敏感性的影响。最初以50mg/kg腹腔注射给予化合物的实验表明,桂利嗪对RIF-1肉瘤经20Gy X射线照射后的细胞存活没有影响,对SCCVII/St癌只有轻微影响。然而,氟桂利嗪在RIF-1肿瘤中产生了轻微的放射增敏作用,在SCCVII/St肿瘤中产生了显著的增敏作用。随后在SCCVII/St肿瘤中的实验表明,氟桂利嗪的最佳放射增敏剂量约为5mg/kg,尽管在0.05-500mg/kg的范围内都有一些增敏作用。氟桂利嗪使X射线剂量反应曲线发生平行移动,相当于缺氧分数降低5倍。在一项正常组织研究中,5mg/kg氟桂利嗪并未增强X射线剂量为2-8Gy时引起的白细胞计数减少。这些数据表明,氟桂利嗪可能有作为放射增敏剂的一些潜在用途。