Stuschke M, Budach V, Klaes W, Sack H
University of Essen, Germany.
Int J Radiat Oncol Biol Phys. 1992;23(1):69-80. doi: 10.1016/0360-3016(92)90545-s.
Radiation doses necessary to control 50% of spheroids (SCD50) were determined for five human soft tissue tumor lines after single dose and fractionated irradiation. Spheroids with 1000-1500 cells were used throughout. A similar number of cells per spheroid resulted in different sized spheroids for the respective cell lines. The parameters alpha, beta, and the number of regenerating cellular units per spheroid (SRU) were estimated from the spheroid control data using a direct fit according to the linear quadratic model assuming Poisson statistics. The number of spheroid regenerating cellular units was also determined from the growth delay at doses required for 10% spheroid control. In addition, alpha, beta, and the fraction of clonogenic cells of the five cell lines were obtained from a soft agar colony forming assay. The most precise parameter for radiation sensitivity was the SCD50, with a coefficient of variation smaller than 5%. SCD50 values ranged from 5.9 to 11.0 Gy for the five soft tissue tumor lines. Two of the five cell lines showed significantly higher alpha values and lower calculated survival fractions after 2 Gy (SF2) in the soft agar clonogenic assay than in the spheroid control assay. This points to a resistance-enhancing effect in the spheroid system. Whereas the fractions of SRU from the number of cells per spheroid, estimated from the spheroid control and growth delay assays, agreed well, no significant correlation existed between the fraction of SRU and the fraction of clonogenic cells in the soft agar colony forming assay. The alpha/beta ratios as a descriptive measure of the fractionation sensitivity of the tumor cell spheroids in the spheroid control assay corresponded well with those derived from the dose-cell survival data using a soft agar colony forming assay. Two of the five cell lines showed high fractionation sensitivities with alpha/beta values smaller than 5 Gy while those of the remaining three ranged from 7.8 to 10.8 Gy. Spheroids are structurally more similar to in vivo tumors than monolayer cultures. From the observed lack of correlation in the radiosensitivity parameters alpha and SF2 as well as in the fraction of SRU or clonogenic cells obtained from the spheroid control assay or the colony forming assay, one would expect even greater differences between results from colony forming assays and the radiosensitivity of in vivo tumors, at least for human soft tissue sarcomas.
对五种人类软组织肿瘤细胞系进行单次照射和分次照射后,测定了控制50%球体(SCD50)所需的辐射剂量。全程使用含1000 - 1500个细胞的球体。每个球体中细胞数量相近,但各细胞系形成的球体大小不同。根据线性二次模型并假设泊松统计,通过直接拟合从球体控制数据中估算出参数α、β以及每个球体中再生细胞单元的数量(SRU)。还根据10%球体控制所需剂量下的生长延迟来确定球体再生细胞单元数量。此外,通过软琼脂集落形成试验获得了这五种细胞系的α、β以及克隆形成细胞的比例。辐射敏感性最精确的参数是SCD50,变异系数小于5%。这五种软组织肿瘤细胞系的SCD50值在5.9至11.0 Gy之间。在软琼脂克隆形成试验中,五个细胞系中有两个显示出比球体控制试验中显著更高的α值以及2 Gy照射后更低的计算存活分数(SF2)。这表明球体系统中有抗性增强效应。虽然从球体控制试验和生长延迟试验估算出的每个球体细胞数量对应的SRU比例吻合良好,但在软琼脂集落形成试验中,SRU比例与克隆形成细胞比例之间不存在显著相关性。在球体控制试验中,作为肿瘤细胞球体分次照射敏感性描述指标的α/β比值,与通过软琼脂集落形成试验从剂量 - 细胞存活数据得出的α/β比值吻合良好。五个细胞系中有两个显示出高分次照射敏感性(α/β值小于5 Gy),而其余三个的α/β值在7.8至10.8 Gy之间。球体在结构上比单层培养物更类似于体内肿瘤。从球体控制试验或集落形成试验获得的辐射敏感性参数α和SF2以及SRU或克隆形成细胞比例之间缺乏相关性来看,至少对于人类软组织肉瘤,人们预计集落形成试验结果与体内肿瘤辐射敏感性之间的差异会更大。