Tindall M J, Please C P, Peddie M J
Mathematical Institute, 24-29 St Giles', Oxford, UK.
Math Biosci. 2008 Jan;211(1):34-55. doi: 10.1016/j.mbs.2007.09.002. Epub 2007 Oct 5.
The mechanisms underlying the formation of necrotic regions within avascular tumours are not well understood. In this paper, we examine the relative roles of nutrient deprivation and of cell death, from both the proliferating phase of the cell cycle via apoptosis and from the quiescent phase via necrosis, in changing the structure within multicellular tumour spheroids and particularly the accumulation of dead cell material in the centre. A mathematical model is presented and studied that accounts for nutrient diffusion, changes in cell cycling rates, the two different routes to cell death as well as active motion of cells and passive motion of the dead cell material. In studying the accumulation of dead cell matter we do not distinguish between the route by which each was formed. The resulting mathematical model is examined for a number of scenarios. Results show that in many cases the size of the necrotic core is closely correlated with low levels in nutrient concentration. However, in certain cases, particularly where the rate of necrosis is large, the resulting necrotic core can lead to regions of non-negligible nutrient concentration-dependent upon the mode of cell death.
血管性肿瘤内坏死区域形成的潜在机制尚未完全明确。在本文中,我们研究了营养物质剥夺和细胞死亡的相对作用,包括从细胞周期的增殖阶段经凋亡导致的细胞死亡,以及从静止阶段经坏死导致的细胞死亡,这些作用如何改变多细胞肿瘤球体的结构,尤其是中心部位死细胞物质的积累情况。我们提出并研究了一个数学模型,该模型考虑了营养物质扩散、细胞周期速率变化、细胞死亡的两种不同途径以及细胞的主动运动和死细胞物质的被动运动。在研究死细胞物质的积累时,我们并未区分每种死细胞物质的形成途径。针对多种情况对所得数学模型进行了检验。结果表明,在许多情况下,坏死核心的大小与低营养浓度密切相关。然而,在某些情况下,特别是坏死速率较大时,所形成的坏死核心会导致出现营养浓度不可忽略的区域,具体情况取决于细胞死亡的模式。