Motivated by experimental observations, we develop a mathematical model of chemotactically directed tumor growth. We present an analytical study of the model as well as a numerical one. The mathematical analysis shows that: (i) tumor cell proliferation by itself cannot generate the invasive branching behavior observed experimentally, (ii) heterotype chemotaxis provides an instability mechanism that leads to the onset of tumor invasion, and (iii) homotype chemotaxis does not provide such an instability mechanism but enhances the mean speed of the tumor surface. The numerical results not only support the assumptions needed to perform the mathematical analysis but they also provide evidence of (i), (ii), and (iii). Finally, both the analytical study and the numerical work agree with the experimental phenomena.
Keywords: immune system competition, multicellular spheroids, theoretical-analysis, capillary formation, factor expression, cell motility, human gliomas, field
Índice de impacto JCR y cuartil WoS: 2.418 (2005); 2.288 (2014)
Referencia DOI: 10.1103/PhysRevE.72.041907
Publicado en papel: Octubre 2005.
M. Castro, C. Molina-Paris, T.S. Deisboeck. Tumor growth instability and the onset of invasio. Physical Review E. vol. 72, no. 4, pp. 041907.1-041907.12, Octubre 2005.