Taubert G, Krug H
Arch Geschwulstforsch. 1986;56(1):1-8.
Based on own investigations general principles of cell cycle analysis by quantitative microscopic methods are discussed. Cell cycle peculiarities of the Ehrlich ascites tumour (EAT) are demonstrated. The numerical data yield information on the underlying type of growth expressed by the logistic function (Verhulst-Pearl). The effective tumour development starts with an exponential phase. In EAT the 5th day is regarded as representative for this stage. Then after a transition phase a steady state is reached. The 11th day after transplantation reflects best this phase of tumour development. By flow cytometric measurements DNA frequency distributions can be obtained in dependence of tumour age. The interpretation of the practically useful height of the second frequency peak in the histograms is discussed in relation to the underlying type of growth. The evaluation of the measurements reveals a characteristic change of the relative duration of the cell cycle phases G1, S, G2 and of the percentage of cells within these phases. Multiparameter single cell measurements complete the cytometric cell cycle analysis in relation to the position of cells in the cell cycle and allow a distinction between quiescent and proliferating cells. Finally the application of the parameters assayed on the biological model is extended to tumours in man.
基于自身研究,讨论了通过定量显微镜方法进行细胞周期分析的一般原则。展示了艾氏腹水瘤(EAT)的细胞周期特性。数值数据提供了关于由逻辑函数(Verhulst-Pearl)表示的潜在生长类型的信息。有效的肿瘤发展始于指数期。在EAT中,第5天被视为该阶段的代表。然后经过一个过渡阶段,达到稳定状态。移植后第11天最能反映肿瘤发展的这个阶段。通过流式细胞术测量,可以获得依赖于肿瘤年龄的DNA频率分布。结合潜在的生长类型,讨论了直方图中第二个频率峰实际有用高度的解释。测量评估揭示了细胞周期阶段G1、S、G2的相对持续时间以及这些阶段内细胞百分比的特征性变化。多参数单细胞测量完善了关于细胞在细胞周期中位置的细胞计量学细胞周期分析,并允许区分静止细胞和增殖细胞。最后,在生物模型上测定的参数的应用扩展到人类肿瘤。