Griffon-Etienne G, Merlin J L, Marchal C
Laboratoire de Recherche en Oncologie, Centre Alexis Vautrin, Vandoeuvre-les-Nancy, France.
Anticancer Drugs. 1997 Jan;8(1):48-55. doi: 10.1097/00001813-199701000-00006.
Taxol cytotoxicity was evaluated in human head and neck squamous carcinoma cell lines growing as multicellular tumor spheroids (MTS) and compared with monolayered culture using conventional clonogenic assays. End points were respectively the concentration inhibiting 50% of the cellular growth (IC50) in clonogenic assays and the concentration required to induce a 50% decrease in the MTS volume (ID50) or number in the overall spheroid population (SCC50). A significant difference was observed when the cells were exposed for 10 days to Taxol as a consequence of the different growth kinetics of the spheroids. After 16 day exposure of spheroids to Taxol, no difference remained between ID50 and IC50. In addition, a significant correlation was found between individual spheroid sensitivity to Taxol (ID50) and the spheroid population sensitivity (SCC50). Both parameters (ID50 and SCC50) defined in cell models appear useful for the evaluation of chemosensitivity of three-dimensional structures known to be closer to in vivo tumor models.
在以多细胞肿瘤球体(MTS)形式生长的人头颈部鳞状癌细胞系中评估了紫杉醇的细胞毒性,并使用传统的克隆形成试验与单层培养进行了比较。终点分别是克隆形成试验中抑制50%细胞生长的浓度(IC50)以及诱导MTS体积减少50%(ID50)或整个球体群体数量减少50%(SCC50)所需的浓度。由于球体不同的生长动力学,当细胞暴露于紫杉醇10天时观察到显著差异。球体暴露于紫杉醇16天后,ID50和IC50之间不再有差异。此外,发现单个球体对紫杉醇的敏感性(ID50)与球体群体敏感性(SCC50)之间存在显著相关性。细胞模型中定义的这两个参数(ID50和SCC50)似乎有助于评估已知更接近体内肿瘤模型的三维结构的化学敏感性。