Cristini Vittorio, Li Xiangrong, Lowengrub John S, Wise Steven M
The University of Texas MD Anderson Cancer Center, School of Health Information Sciences, University of Texas Health Science Center, Houston, TX 77030, USA.
J Math Biol. 2009 Apr;58(4-5):723-63. doi: 10.1007/s00285-008-0215-x. Epub 2008 Sep 12.
We develop a thermodynamically consistent mixture model for avascular solid tumor growth which takes into account the effects of cell-to-cell adhesion, and taxis inducing chemical and molecular species. The mixture model is well-posed and the governing equations are of Cahn-Hilliard type. When there are only two phases, our asymptotic analysis shows that earlier single-phase models may be recovered as limiting cases of a two-phase model. To solve the governing equations, we develop a numerical algorithm based on an adaptive Cartesian block-structured mesh refinement scheme. A centered-difference approximation is used for the space discretization so that the scheme is second order accurate in space. An implicit discretization in time is used which results in nonlinear equations at implicit time levels. We further employ a gradient stable discretization scheme so that the nonlinear equations are solvable for very large time steps. To solve those equations we use a nonlinear multilevel/multigrid method which is of an optimal order O(N) where N is the number of grid points. Spherically symmetric and fully two dimensional nonlinear numerical simulations are performed. We investigate tumor evolution in nutrient-rich and nutrient-poor tissues. A number of important results have been uncovered. For example, we demonstrate that the tumor may suffer from taxis-driven fingering instabilities which are most dramatic when cell proliferation is low, as predicted by linear stability theory. This is also observed in experiments. This work shows that taxis may play a role in tumor invasion and that when nutrient plays the role of a chemoattractant, the diffusional instability is exacerbated by nutrient gradients. Accordingly, we believe this model is capable of describing complex invasive patterns observed in experiments.
我们开发了一种用于无血管实体肿瘤生长的热力学一致混合模型,该模型考虑了细胞间粘附以及诱导趋化作用的化学和分子物质的影响。该混合模型是适定的,控制方程为Cahn-Hilliard型。当只有两相时,我们的渐近分析表明,早期的单相模型可以作为两相模型的极限情况恢复。为了求解控制方程,我们基于自适应笛卡尔块结构网格细化方案开发了一种数值算法。空间离散化采用中心差分近似,使得该方案在空间上具有二阶精度。时间上采用隐式离散化,这导致在隐式时间层上出现非线性方程。我们进一步采用梯度稳定离散化方案,以便对于非常大的时间步长,非线性方程是可解的。为了求解这些方程,我们使用一种非线性多层/多重网格方法,其具有最优阶O(N),其中N是网格点的数量。进行了球对称和全二维非线性数值模拟。我们研究了肿瘤在营养丰富和营养贫乏组织中的演化。发现了许多重要结果。例如,我们证明肿瘤可能会遭受趋化作用驱动的指进不稳定性,正如线性稳定性理论所预测的,当细胞增殖较低时,这种不稳定性最为显著。这在实验中也得到了观察。这项工作表明趋化作用可能在肿瘤侵袭中起作用,并且当营养物质起化学引诱剂的作用时,扩散不稳定性会因营养物质梯度而加剧。因此,我们相信这个模型能够描述实验中观察到的复杂侵袭模式。