Mathematical modeling of tumor-induced angiogenesis

被引:193
|
作者
Chaplain, M. A. J. [1 ]
McDougall, S. R.
Anderson, A. R. A.
机构
[1] Univ Dundee, SIMBIOSIS Ctr, Div Math, Dundee DD1 4HN, Scotland
[2] Heriot Watt Univ, Inst Petr Engn, Edinburgh EH14 4AS, Midlothian, Scotland
关键词
blood vessels; microvasculature; endothelial cell migration; network flow; drug delivery;
D O I
10.1146/annurev.bioeng.8.061505.095807
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Angiogenesis, the growth of a network of blood vessels, is a crucial component of solid tumor growth, linking the relatively harmless avascular and the potentially fatal vascular growth phases of the tumor.. As a process, angiogenesis is a well-orchestrated sequence of events involving endothelial cell migration and proliferation; degradation of tissue; new capillary vessel formation; loop formation (anastomosis) and, crucially, blood flow through the network. Once there is flow associated with the nascent network, subsequent growth evolves both temporally and spatially in response to the combined effects of angiogenic factors, migratory cues via the extracellular matrix, and perfusion-related hemodynamic forces in a manner that may be described as both adaptive and dynamic. In this article, we first present a review of previous theoretical and computational models of angiogenesis and then indicate how recent developments in flow models are providing insight into anti-angiogenic and chemotherapeutic drug treatment of solid tumors.
引用
收藏
页码:233 / 257
页数:25
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