Duchesne G M, Peacock J H
Int J Radiat Biol Relat Stud Phys Chem Med. 1987 Feb;51(2):365-75. doi: 10.1080/09553008714550831.
The radiation sensitivity of two small-cell lung carcinoma cell lines growing as multicellular spheroids in static culture was determined using clonogenic cell survival and growth delay as endpoints. Growth delay determination suggested that clonogenic cell kill was less than was obtained by direct assay of cell survival. Recovery from potentially lethal damage was assayed in one line (HC12) but was not demonstrable, and clonogenic cell survival decreased with time in treated spheroids with diameters greater than 300 microns which contained a hypoxic cell population. Microscopic examination of the treated spheroids showed the emergence of an abnormal giant-cell population, and the progressive clonogenic cell loss that occurred after treatment was thought to be due to oxygen and nutrient deprivation of the remaining viable cells by this doomed cell population. Correction of the growth delay measurements for changes in cell size and clonogenic cell population allowed correlation of the growth delay and cell survival data.
使用克隆形成细胞存活和生长延迟作为终点指标,测定了在静态培养中以多细胞球体形式生长的两种小细胞肺癌细胞系的辐射敏感性。生长延迟测定表明,克隆形成细胞杀伤低于通过直接检测细胞存活所获得的结果。在其中一个细胞系(HC12)中检测了潜在致死性损伤的修复情况,但未得到证实,并且在直径大于300微米且含有缺氧细胞群体的经处理球体中,克隆形成细胞存活随时间下降。对经处理球体的显微镜检查显示出现了异常的巨细胞群体,并且认为处理后发生的克隆形成细胞逐渐丧失是由于这个注定死亡的细胞群体对剩余活细胞的氧气和营养剥夺所致。对细胞大小和克隆形成细胞群体变化的生长延迟测量进行校正后,可将生长延迟和细胞存活数据进行关联。