Literature DB >> 11800713

Diffusion with evolving sources and competing sinks: development of angiogenesis.

M Scalerandi1, B Capogrosso Sansone, C A Condat.   

Abstract

Tumors ensure their long-time growth by emitting molecular messengers that induce cellular modifications in neighboring capillaries. These modifications are conducive to the enlargement of the vascular system feeding the tumor. This phenomenon, termed angiogenesis, is controlled by the diffusion and competitive trapping of nutrients and molecular messengers by several cell species. The number, location, and properties of these traps change continuously. The angiogenic process also implies that nutrient sources are time dependent. Starting from assumptions at the cellular level, we formulate a mathematical model that predicts the evolution of angiogenesis and the increase in the blood flow to the tumor. The model also predicts the emergence of directed growth and the possibility of therapeutical synergy. Simulations permit a careful analysis of the influence of the main parameters.

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Year:  2001        PMID: 11800713     DOI: 10.1103/PhysRevE.65.011902

Source DB:  PubMed          Journal:  Phys Rev E Stat Nonlin Soft Matter Phys        ISSN: 1539-3755


  4 in total

1.  Diversity of dynamics and morphologies of invasive solid tumors.

Authors:  Yang Jiao; Salvatore Torquato
Journal:  AIP Adv       Date:  2012-03-21       Impact factor: 1.548

Review 2.  Computational and mathematical modeling of angiogenesis.

Authors:  Shayn M Peirce
Journal:  Microcirculation       Date:  2008-11       Impact factor: 2.628

3.  Emergent behaviors from a cellular automaton model for invasive tumor growth in heterogeneous microenvironments.

Authors:  Yang Jiao; Salvatore Torquato
Journal:  PLoS Comput Biol       Date:  2011-12-22       Impact factor: 4.475

4.  Properties of tumor spheroid growth exhibited by simple mathematical models.

Authors:  Dorothy I Wallace; Xinyue Guo
Journal:  Front Oncol       Date:  2013-03-15       Impact factor: 6.244

  4 in total

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