首页> 美国卫生研究院文献>Analytical Cellular Pathology : the Journal of the European Society for Analytical Cellular Pathology >Cellular Automaton Simulation of Tumour Growth – Equivocal Relationships between Simulation Parameters and Morphologic Pattern Features
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Cellular Automaton Simulation of Tumour Growth – Equivocal Relationships between Simulation Parameters and Morphologic Pattern Features

机译:肿瘤生长的细胞自动机模拟-模拟参数与形态特征之间的模棱两可关系

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摘要

Objective: To develop an interpretation procedure which estimates simulation parameters (tumour cell motility, tumour cell adhesion, autocrine and paracrine growth control, stroma destruction) of simulated patterns solely based on morphometric features of the morphologic pattern. Methods: A cellular automaton computer simulation program was developed which produces morphologic patterns by growth of a seed of tumour cells. At the beginning of each simulation run certain simulation parameters are assigned to the tumour cells. After the run has been completed, the resulting pattern is evaluated by a set of morphometric features. Simulation parameters and resulting morphometric features of 27,800 simulations were stored in a database and were used for the evaluation of potential relationships. Results: Correlation analysis showed highly significant correlations between morphometric features on the one hand and the preset simulation parameters (tumour cell motility, tumour cell adhesion, autocrine and paracrine growth control, stroma destruction) on the other. Correlation coefficients, however, varied from 0.72 to 0.99. When only one simulation parameter varied while all others were kept constant, morphometric features yielded a highly reliable estimate of the particular simulation parameter. When variability was extended to 4 simulation parameters, morphometric features were less effective in estimating the setting of the parameters. Though in all patterns tested several possible simulation parameter constellations could be ruled out, morphometric features were usually compatible with more than one set of simulation parameters thus preventing a straightforward interpretation. Conclusions: Though simulation parameters significantly and reproducibly influence the resulting morphologic pattern as characterized by morphometric features, estimates of the simulation parameters based on morphometric features yield equivocal results.
机译:目的:开发一种解释程序,仅根据形态模式的形态特征来估计模拟模式的模拟参数(肿瘤细胞运动性,肿瘤细胞粘附,自分泌和旁分泌生长控制,基质破坏)。方法:开发了一种细胞自动机计算机仿真程序,该程序通过肿瘤细胞种子的生长产生形态学模式。在每次模拟开始时,将某些模拟参数分配给肿瘤细胞。运行完成后,将通过一组形态计量特征来评估所得图案。 27,800个模拟的模拟参数和所得形态特征存储在数据库中,并用于评估潜在关系。结果:相关性分析一方面显示了形态特征与预设的模拟参数(肿瘤细胞运动性,肿瘤细胞粘附,自分泌和旁分泌生长控制,基质破坏)之间的高度显着相关性。但是,相关系数在0.72至0.99之间变化。当只有一个仿真参数变化而所有其他仿真参数保持不变时,形态计量学特征就可以得出特定仿真参数的高度可靠的估计值。当将可变性扩展到4个模拟参数时,形态特征在估计参数设置方面不太有效。尽管在所有测试的模式中都可以排除几种可能的模拟参数星座,但是形态特征通常与多于一组的模拟参数兼容,因此妨碍了直接的解释。结论:尽管仿真参数显着且可再现地影响以形态计量特征为特征的最终形态模式,但基于形态计量特征的模拟参数估计却产生了模棱两可的结果。

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