Tindall M J, Please C P
Mathematical Institute, 24-29 St Giles', Oxford, UK.
Bull Math Biol. 2007 May;69(4):1147-65. doi: 10.1007/s11538-006-9110-z. Epub 2007 Mar 20.
This paper analyses a recent mathematical model of avascular tumour spheroid growth which accounts for both cell cycle dynamics and chemotactic driven cell movement. The model considers cells to exist in one of two compartments: proliferating and quiescent, as well as accounting for necrosis and apoptosis. One particular focus of this paper is the behaviour created when proliferating and quiescent cells have different chemotactic responses to an extracellular nutrient supply. Two very different steady-state behaviours are identified corresponding to those cases where proliferating cells move either more quickly or more slowly than quiescent cells in response to a gradient in the extracellular nutrient supply. The case where proliferating cells move more rapidly leads to the commonly accepted spheroid structure of a thin layer of proliferating cells surrounding an inner quiescent core. In the case where proliferating cells move more slowly than quiescent cells the model predicts an interesting structure of a thin layer of quiescent cells surrounding an inner core of proliferating and quiescent cells. The sensitivity of this tumour structure to the cell cycle model parameters is also discussed. In particular variations in the steady-state size of the tumour and the types of transient behaviour are explored. The model reveals interesting transient behaviour with sharply delineated regions of proliferating and quiescent cells.
本文分析了一种最近的无血管肿瘤球体生长数学模型,该模型兼顾了细胞周期动力学和趋化性驱动的细胞运动。该模型认为细胞存在于两个区室之一:增殖区室和静止区室,同时也考虑了坏死和凋亡。本文的一个特别关注点是当增殖细胞和静止细胞对细胞外营养供应具有不同趋化反应时所产生的行为。识别出了两种截然不同的稳态行为,分别对应于增殖细胞在细胞外营养供应梯度作用下比静止细胞移动更快或更慢的情况。增殖细胞移动更快的情况会导致形成一种普遍认可的球体结构,即围绕内部静止核心的一层薄薄的增殖细胞。在增殖细胞比静止细胞移动更慢的情况下,该模型预测会形成一种有趣的结构,即围绕增殖细胞和静止细胞内部核心的一层薄薄的静止细胞。还讨论了这种肿瘤结构对细胞周期模型参数的敏感性。特别是探讨了肿瘤稳态大小的变化以及瞬态行为的类型。该模型揭示了具有增殖细胞和静止细胞清晰界定区域的有趣瞬态行为。