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多细胞肿瘤球体生长的预测:对实体瘤动态生长的影响。

Forecasting the growth of multicell tumour spheroids: implications for the dynamic growth of solid tumours.

作者信息

Chignola R, Schenetti A, Andrighetto G, Chiesa E, Foroni R, Sartoris S, Tridente G, Liberati D

机构信息

Department of Pathology, University of Verona, Italy.

出版信息

Cell Prolif. 2000 Aug;33(4):219-29. doi: 10.1046/j.1365-2184.2000.00174.x.

Abstract

The growth dynamics of multicell tumour spheroids (MTS) were analysed by means of mathematical techniques derived from signal processing theory. Volume vs. time trajectories of individual spheroids were fitted with the Gompertz growth equation and the residuals (i.e. experimental volume determinations minus calculated values by fitting) were analysed by fast fourier transform and power spectrum. Residuals were not randomly distributed around calculated growth trajectories demonstrating that the Gompertz model partially approximates the growth kinetics of three-dimensional tumour cell aggregates. Power spectra decreased with increasing frequency following a 1/f(delta) power-law. Our findings suggest the existence of a source of 'internal' variability driving the time-evolution of MTS growth. Based on these observations, a new stochastic Gompertzian-like mathematical model was developed which allowed us to forecast the growth of MTS. In this model, white noise is additively superimposed to the trend described by the Gompertz growth equation and integrated to mimic the observed intrinsic variability of MTS growth. A correlation was found between the intensity of the added noise and the particular upper limit of volume size reached by each spheroid within two MTS populations obtained with two different cell lines. The dynamic forces generating the growth variability of three-dimensional tumour cell aggregates also determine the fate of spheroid growth with a strong predictive significance. These findings suggest a new approach to measure tumour growth potential.

摘要

利用源自信号处理理论的数学技术分析了多细胞肿瘤球体(MTS)的生长动力学。将单个球体的体积与时间轨迹用Gompertz生长方程拟合,并通过快速傅里叶变换和功率谱分析残差(即实验体积测定值减去拟合计算值)。残差并非围绕计算出的生长轨迹随机分布,这表明Gompertz模型部分近似三维肿瘤细胞聚集体的生长动力学。功率谱随频率增加按照1/f(δ)幂律下降。我们的研究结果表明存在一种“内部”变异性来源驱动MTS生长的时间演变。基于这些观察结果,开发了一种新的类似Gompertz的随机数学模型,该模型使我们能够预测MTS的生长。在该模型中,白噪声被叠加到由Gompertz生长方程描述的趋势上并进行积分,以模拟观察到的MTS生长的内在变异性。在所获得的两个不同细胞系的两个MTS群体中,发现添加噪声的强度与每个球体达到的特定体积大小上限之间存在相关性。产生三维肿瘤细胞聚集体生长变异性的动力也决定了球体生长的命运,具有很强的预测意义。这些发现提出了一种测量肿瘤生长潜力的新方法。

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