A dynamic model for tumour growth and metastasis formation.

Volker Haustein, Udo Schumacher
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引用次数: 23

Abstract

A simple and fast computational model to describe the dynamics of tumour growth and metastasis formation is presented. The model is based on the calculation of successive generations of tumour cells and enables one to describe biologically important entities like tumour volume, time point of 1st metastatic growth or number of metastatic colonies at a given time. The model entirely relies on the chronology of these successive events of the metastatic cascade. The simulation calculations were performed for two embedded growth models to describe the Gompertzian like growth behaviour of tumours. The initial training of the models was carried out using an analytical solution for the size distribution of metastases of a hepatocellular carcinoma. We then show the applicability of our models to clinical data from the Munich Cancer Registry. Growth and dissemination characteristics of metastatic cells originating from cells in the primary breast cancer can be modelled thus showing its ability to perform systematic analyses relevant for clinical breast cancer research and treatment. In particular, our calculations show that generally metastases formation has already been initiated before the primary can be detected clinically.

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肿瘤生长和转移形成的动态模型。
提出了一个简单、快速的计算模型来描述肿瘤生长和转移形成的动力学过程。该模型基于对肿瘤细胞连续代的计算,使人们能够描述生物学上重要的实体,如肿瘤体积、第一次转移生长的时间点或在给定时间转移菌落的数量。该模型完全依赖于这些转移级联的连续事件的年表。模拟计算是对两个嵌入式生长模型进行的,以描述肿瘤的冈伯兹样生长行为。模型的初始训练是使用肝细胞癌转移灶大小分布的解析解进行的。然后,我们展示了我们的模型对慕尼黑癌症登记处临床数据的适用性。源自原发性乳腺癌细胞的转移细胞的生长和传播特征可以建模,从而显示其进行与乳腺癌临床研究和治疗相关的系统分析的能力。特别是,我们的计算表明,通常转移形成已经开始之前,原发可以检测到临床。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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