Article
An evolutionary hybrid cellular automaton model of solid tumour growth.
Division of Mathematics, University of Dundee, Dundee, UK.
Journal of Theoretical Biology (impact factor:
2.21).
07/2007;
246(4):583-603.
DOI:10.1016/j.jtbi.2007.01.027
pp.583-603
Source: PubMed
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Article: Hypoxia selects for high-metastatic Lewis lung carcinoma cells overexpressing Mcl-1 and exhibiting reduced apoptotic potential in solid tumors.
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ABSTRACT: Low oxygen tension (hypoxia) is a common feature of solid tumors and stimulates the expressions of a variety of genes including those related to angiogenesis, apoptosis and endoplasmic reticulum (ER) stress response. Here we show a close correlation between metastatic potential and the resistance to hypoxia- and ER stress-induced apoptosis among the cell lines with differing metastatic potential derived from Lewis lung carcinoma. An apoptosis-specific expression profiling and immunoblot analyses revealed that the expression of antiapoptotic Mcl-1 increased as the resistance to apoptosis increased. Downregulation of the Mcl-1 expression in the high-metastatic cells by Mcl-1 small interfering RNA increased the sensitivity to hypoxia-induced apoptosis and decreased the metastatic ability. The hypoxia-induced apoptosis was not associated with p53 accumulation, although at present it is not possible to conclude that apoptosis-induced apoptosis is p53-independent. There was no correlation between the expression levels of ER stress-response proteins GADD153, GRP78 and ORP150 and the resistance to hypoxia or ER stresses. In vitro, small numbers of the high-metastatic cells overtook the low-metastatic cells after exposure to several rounds of hypoxia and reoxygenation. In solid tumors initially established from equal mixtures, the proportion of the high-metastatic cells to low-metastatic cells was significantly higher in hypoxic areas. Moreover, the high-metastatic cells were overtaking the low-metastatic cells in some of the tumors. Thus, tumor hypoxia and ER stress may provide a physiological selective pressure for the expansion of the high-metastatic cells overexpressing Mcl-1 and exhibiting reduced apoptotic potential in solid tumors.Oncogene 03/2006; 25(6):917-28. · 6.37 Impact Factor
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Keywords
available space
cell population diversity
cells divide
cellular automaton model
cellular behaviour
clonal evolution
connection weights
contains aggressive phenotypes
evolutionary dynamics
feed-forward artificial neural network
fittest cells
low oxygen concentration
micro-environment response network
morphological level
oxygen concentration
selection pressure
solid tumour growth
takes environmental variables
tissue oxygen concentration