Grdina D J, Sigdestad C P, Peters L J
Br J Cancer. 1979 Feb;39(2):152-8. doi: 10.1038/bjc.1979.25.
The S-phase-specific cytotoxicity of hydroxyurea (HU) was tested on synchronized murine fibrosarcoma (FSa) cells lodged in the lungs of C3Hf/Bu mice. FSa cells from primary asynchronous cultures were separated and synchronized on the basis of size by centrifugal elutriation. Flow microfluorometry (FMF) was used to determine the cell-cycle parameters and the relative synchrony of the separated populations. After elutriation, 8000 viable FSa cells from each fraction, along with 10(6) heavily irradiated tumour cells (unseparated) were injected i.v. into whole-body-irradiated mice (20 per group). Under these conditions, 95% of the injected cells, regardless of size or position in the cell cycle, are arrested in the lungs. Twenty minutes later, hydroxyurea (HU, 1 mg/g) was administered i.p. into 10 animals of each group. Fourteen days later the animals were killed, their lungs removed and fixed, and the number of macroscopic tumour nodules counted. Killing of the initially injected cells by HU, as evidenced by a reduction in lung colonies in treated animals, correlated with the precentage of S-phase cells in each fraction. The greatest effect, an 80% reduction in colony number, was seen in Fraction 8, containing the largest percentage of S-phase cells (65%). These results demonstrate the usefulness of this procedure as a rapid method for characterizing the phase specificity of chemotherapeutic drugs in vivo.
在C3Hf/Bu小鼠肺中植入的同步化鼠纤维肉瘤(FSa)细胞上测试了羟基脲(HU)的S期特异性细胞毒性。将来自原代非同步培养物的FSa细胞通过离心淘析根据大小进行分离和同步化。使用流式细胞荧光测定法(FMF)来确定细胞周期参数以及分离群体的相对同步性。淘析后,将来自每个组分的8000个活的FSa细胞与10⁶个重度照射的肿瘤细胞(未分离)静脉注射到全身照射的小鼠体内(每组20只)。在这些条件下,无论细胞大小或在细胞周期中的位置如何,95%的注入细胞会滞留在肺部。20分钟后,向每组的10只动物腹腔注射羟基脲(HU,1mg/g)。14天后处死动物,取出并固定它们的肺,然后计数肉眼可见的肿瘤结节数量。治疗动物肺部集落减少证明HU对最初注入细胞的杀伤作用与每个组分中S期细胞的百分比相关。在含有最大百分比S期细胞(65%)的第8组分中观察到最大的效果,集落数量减少了80%。这些结果证明了该程序作为一种在体内表征化疗药物阶段特异性的快速方法的有用性。