Angiogenesis and vessel co-option in a mathematical model of diffusive tumor growth: The role of chemotaxis

JOURNAL OF THEORETICAL BIOLOGY

卷:512

Article

Gandolfi, A.⁶  De Franciscis, S.¹  d'Onofrio, A.^2,3  Fasano, A.^4,5,6  Sinisgalli, C.⁶ 

[1] Inst Astrofis Andalucia IAA CSIC, Granada, Spain

[2] Int Prevent Res Inst, Lyon, France

[3] Strathclyde Univ, Dept Math & Stat, Glasgow, Lanark, Scotland

[4] Univ Firenze, Dipartimento Matemat U Dini, Florence, Italy

[5] FIAB SpA, Florence, Italy

[6] Ist Anal Sistemi & Informat A Ruberti CNR, Rome, Italy

关键词: Modeling vascularized tumor growth;    Angiogenesis;    Chemotaxis;    Tumor invasion;    Traveling waves;    Fickian diffusion;   

DOI  :  10.1016/j.jtbi.2020.110526

来源: Elsevier

【 摘 要 】

This work considers the propagation of a tumor from the stage of a small avascular sphere in a host tissue and the progressive onset of a tumor neovasculature stimulated by a pro-angiogenic factor secreted by hypoxic cells. The way new vessels are formed involves cell sprouting from pre-existing vessels and following a trail via a chemotactic mechanism (CM). Namely, it is first proposed a detailed general family of models of the CM, based on a statistical mechanics approach. The key hypothesis is that the CM is composed by two components: i) the well-known bias induced by the angiogenic factor gradient; ii) the presence of stochastic changes of the velocity direction, thus giving rise to a diffusive component. Then, some further assumptions and simplifications are applied in order to derive a specific model to be used in the simulations. The tumor progression is favored by its acidic aggression towards the healthy cells. The model includes the evolution of many biological and chemical species. Numerical simulations show the onset of a traveling wave eventually replacing the host tissue with a fully vascularized tumor. The results of simulations agree with experimental measures of the vasculature density in tumors, even in the case of particularly hypoxic tumors. (C) 2020 Elsevier Ltd. All rights reserved.

【 授权许可】

Free