On the mean field approximation of a stochastic model of tumour-induced angiogenesis

被引:7
|
作者
Capasso, V [1 ]
Flandoli, F. [2 ]
机构
[1] Univ Milano La Statale, ADAMSS, Via Saldini 50, I-20133 Milan, Italy
[2] Scuola Normale Super Pisa, Piazza Cavalieri 7, Pisa, Italy
关键词
Cell movement; Interacting particle systems; Convergence of probability measures; PDEs in connection with biology and other natural sciences; Stochastic analysis;
D O I
10.1017/S0956792518000347
中图分类号
O29 [应用数学];
学科分类号
070104 ;
摘要
In the field of Life Sciences, it is very common to deal with extremely complex systems, from both analytical and computational points of view, due to the unavoidable coupling of different interacting structures. As an example, angiogenesis has revealed to be an highly complex, and extremely interesting biomedical problem, due to the strong coupling between the kinetic parameters of the relevant branching - growth - anastomosis stochastic processes of the capillary network, at the microscale, and the family of interacting underlying biochemical fields, at the macroscale. In this paper, an original revisited conceptual stochastic model of tumour-driven angiogenesis has been proposed, for which it has been shown that it is possible to reduce complexity by taking advantage of the intrinsic multiscale structure of the system; one may keep the stochasticity of the dynamics of the vessel tips at their natural microscale, whereas the dynamics of the underlying fields is given by a deterministic mean field approximation obtained by an averaging at a suitable mesoscale. While in previous papers, only an heuristic justification of this approach had been offered; in this paper, a rigorous proof is given of the so called 'propagation of chaos', which leads to a mean field approximation of the stochastic relevant measures associated with the vessel dynamics, and consequently of the underlying tumour angiogenic factor (TAF) field. As a side, though important result, the non-extinction of the random process of tips has been proven during any finite time interval.
引用
收藏
页码:619 / 658
页数:40
相关论文
共 50 条
  • [1] Stochastic modelling of tumour-induced angiogenesis
    Vincenzo Capasso
    Daniela Morale
    [J]. Journal of Mathematical Biology, 2009, 58 : 219 - 233
  • [2] Stochastic modelling of tumour-induced angiogenesis
    Capasso, Vincenzo
    Morale, Daniela
    [J]. JOURNAL OF MATHEMATICAL BIOLOGY, 2009, 58 (1-2) : 219 - 233
  • [3] Stochastic geometric models, and related statistical issues in tumour-induced angiogenesis
    Capasso, Vincenzo
    Micheletti, Alessandra
    Morale, Daniela
    [J]. MATHEMATICAL BIOSCIENCES, 2008, 214 (1-2) : 20 - 31
  • [4] Quantification of tumour-induced angiogenesis by image analysis
    Iwahana, M
    Nakayama, Y
    Tanaka, NG
    Goryo, M
    Okada, K
    [J]. INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 1996, 77 (03) : 109 - 114
  • [5] Earliest stages of tumour-induced angiogenesis dissected
    Bosch, X
    [J]. LANCET, 2000, 355 (9201): : 382 - 382
  • [6] Mathematical modelling, simulation and prediction of tumour-induced angiogenesis
    Chaplain, MAJ
    Anderson, ARA
    [J]. INVASION & METASTASIS, 1996, 16 (4-5): : 222 - 234
  • [7] Towards a two-scale cellular automata model of tumour-induced angiogenesis
    Topa, Pawel
    [J]. CELLULAR AUTOMATA, PROCEEDINGS, 2006, 4173 : 337 - 346
  • [8] Modelling of tumour-induced angiogenesis with regress by immune factor
    Chen, Wei
    Zhang, Li
    Shao, Ling
    Bass, Rosemary
    Liu, Chenyu
    Hossain, Alamgir
    [J]. 2015 9TH INTERNATIONAL CONFERENCE ON SOFTWARE, KNOWLEDGE, INFORMATION MANAGEMENT AND APPLICATIONS (SKIMA), 2015,
  • [9] A Current Perspective on Wound Healing and Tumour-Induced Angiogenesis
    Jennifer A. Flegg
    Shakti N. Menon
    Helen M. Byrne
    D. L. Sean McElwain
    [J]. Bulletin of Mathematical Biology, 2020, 82
  • [10] A Current Perspective on Wound Healing and Tumour-Induced Angiogenesis
    Flegg, Jennifer A.
    Menon, Shakti N.
    Byrne, Helen M.
    McElwain, D. L. Sean
    [J]. BULLETIN OF MATHEMATICAL BIOLOGY, 2020, 82 (02)