Wayss K, Mattern J, Volm M
Strahlentherapie. 1980 Jan;156(1):41-5.
Sprague-Dawley rats with solid Walker carcino-sarcomas were synchronized with hydroxyurea (HU; 6 x 50 mg and 1 x 300 mg HU/kg body weight) and then irradiated at different time points (60Co). The synchronized tumors showed a significant delay of growth when irradiation was applied in the late G1 phase, at the transition G1/S and in the early S phase. The remaining phases of the cell cycle, especially the S phase showed the same sensitivity as the non-synchronized controls. Improvement of therapy by irradiation after HU application was largely due to the synchronization of tumor cells. Only the increased therapeutic effect of irradiation shortly after application of HU can be explained also by combination of both HU and irradiation.
将患有实体Walker癌肉瘤的Sprague-Dawley大鼠用羟基脲(HU;6×50mg和1×300mg HU/千克体重)同步化,然后在不同时间点(60Co)进行照射。当在G1期晚期、G1/S期转换点和S期早期进行照射时,同步化的肿瘤显示出生长显著延迟。细胞周期的其余阶段,尤其是S期,与未同步化的对照组表现出相同的敏感性。HU应用后通过照射改善治疗效果很大程度上归因于肿瘤细胞的同步化。HU应用后不久照射治疗效果的增加也可以通过HU和照射两者的联合作用来解释。