Grdina D J
Br J Cancer. 1982 Mar;45(3):438-46. doi: 10.1038/bjc.1982.72.
The cytotoxic effects in vivo of hydroxyurea (HU) on murine fibrosarcoma (FSa) cells grown as pulmonary tumours were determined. Tumour cells from 13-day-old nodules were made into suspension and separated on the basis of cell size by centrifugal elutriation. Flow microfluorometry (FMF) was used to determine the cell-cycle parameters and the relative synchrony of the separated populations, as well as the degree of contamination by normal diploid cells in each of the tumour-cell populations. HU cytotoxicity was tested by administering both a single 1 mg/g i.p. dose into mice that had been injected i.v. 20 min earlier with known numbers of synchronized viable FSa cells, and i.p. doses of 1 mg/g each into mice bearing 13-day-old pulmonary nodules. In the latter experiments, animals were killed 1 h after the last dose, and the tumour nodules were excised and made into a single-cell suspension and elutriated. Known numbers of cells from each fraction were injected into recipient mice to determine survival. In both sets of experiments, cell killing by HU correlated with the percentage of S-phase cells. The treatment of 13-day-old pulmonary nodules with 3 doses of HU also depleted the (G2+M) phase tumour cells and increased the heterogeneity between tumour subpopulations, as determined by FMF analysis.
测定了羟基脲(HU)对作为肺肿瘤生长的小鼠纤维肉瘤(FSa)细胞的体内细胞毒性作用。将来自13日龄结节的肿瘤细胞制成悬液,并通过离心淘析根据细胞大小进行分离。采用流式细胞荧光测定法(FMF)来确定分离群体的细胞周期参数和相对同步性,以及每个肿瘤细胞群体中正常二倍体细胞的污染程度。通过向20分钟前经静脉注射已知数量同步化活FSa细胞的小鼠腹腔注射单次1 mg/g剂量,以及向携带13日龄肺结节的小鼠腹腔注射每次1 mg/g剂量来测试HU的细胞毒性。在后一组实验中,在最后一剂后1小时处死动物,切除肿瘤结节并制成单细胞悬液并进行淘析。将各部分已知数量的细胞注射到受体小鼠中以确定存活率。在两组实验中,HU导致的细胞杀伤均与S期细胞百分比相关。如通过FMF分析所确定的,用3剂HU处理13日龄肺结节也使(G2+M)期肿瘤细胞减少,并增加了肿瘤亚群之间的异质性。