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Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration

Understanding the etiology of metastasis is very important in clinical perspective, since it is estimated that metastasis accounts for 90% of cancer patient mortality. Metastasis results from a sequence of multiple steps including invasion and migration. The early stages of metastasis are tightly co...

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Autores principales: Cohen, David P. A., Martignetti, Loredana, Robine, Sylvie, Barillot, Emmanuel, Zinovyev, Andrei, Calzone, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631357/
https://www.ncbi.nlm.nih.gov/pubmed/26528548
http://dx.doi.org/10.1371/journal.pcbi.1004571
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author Cohen, David P. A.
Martignetti, Loredana
Robine, Sylvie
Barillot, Emmanuel
Zinovyev, Andrei
Calzone, Laurence
author_facet Cohen, David P. A.
Martignetti, Loredana
Robine, Sylvie
Barillot, Emmanuel
Zinovyev, Andrei
Calzone, Laurence
author_sort Cohen, David P. A.
collection PubMed
description Understanding the etiology of metastasis is very important in clinical perspective, since it is estimated that metastasis accounts for 90% of cancer patient mortality. Metastasis results from a sequence of multiple steps including invasion and migration. The early stages of metastasis are tightly controlled in normal cells and can be drastically affected by malignant mutations; therefore, they might constitute the principal determinants of the overall metastatic rate even if the later stages take long to occur. To elucidate the role of individual mutations or their combinations affecting the metastatic development, a logical model has been constructed that recapitulates published experimental results of known gene perturbations on local invasion and migration processes, and predict the effect of not yet experimentally assessed mutations. The model has been validated using experimental data on transcriptome dynamics following TGF-β-dependent induction of Epithelial to Mesenchymal Transition in lung cancer cell lines. A method to associate gene expression profiles with different stable state solutions of the logical model has been developed for that purpose. In addition, we have systematically predicted alleviating (masking) and synergistic pairwise genetic interactions between the genes composing the model with respect to the probability of acquiring the metastatic phenotype. We focused on several unexpected synergistic genetic interactions leading to theoretically very high metastasis probability. Among them, the synergistic combination of Notch overexpression and p53 deletion shows one of the strongest effects, which is in agreement with a recent published experiment in a mouse model of gut cancer. The mathematical model can recapitulate experimental mutations in both cell line and mouse models. Furthermore, the model predicts new gene perturbations that affect the early steps of metastasis underlying potential intervention points for innovative therapeutic strategies in oncology.
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spelling pubmed-46313572015-11-13 Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration Cohen, David P. A. Martignetti, Loredana Robine, Sylvie Barillot, Emmanuel Zinovyev, Andrei Calzone, Laurence PLoS Comput Biol Research Article Understanding the etiology of metastasis is very important in clinical perspective, since it is estimated that metastasis accounts for 90% of cancer patient mortality. Metastasis results from a sequence of multiple steps including invasion and migration. The early stages of metastasis are tightly controlled in normal cells and can be drastically affected by malignant mutations; therefore, they might constitute the principal determinants of the overall metastatic rate even if the later stages take long to occur. To elucidate the role of individual mutations or their combinations affecting the metastatic development, a logical model has been constructed that recapitulates published experimental results of known gene perturbations on local invasion and migration processes, and predict the effect of not yet experimentally assessed mutations. The model has been validated using experimental data on transcriptome dynamics following TGF-β-dependent induction of Epithelial to Mesenchymal Transition in lung cancer cell lines. A method to associate gene expression profiles with different stable state solutions of the logical model has been developed for that purpose. In addition, we have systematically predicted alleviating (masking) and synergistic pairwise genetic interactions between the genes composing the model with respect to the probability of acquiring the metastatic phenotype. We focused on several unexpected synergistic genetic interactions leading to theoretically very high metastasis probability. Among them, the synergistic combination of Notch overexpression and p53 deletion shows one of the strongest effects, which is in agreement with a recent published experiment in a mouse model of gut cancer. The mathematical model can recapitulate experimental mutations in both cell line and mouse models. Furthermore, the model predicts new gene perturbations that affect the early steps of metastasis underlying potential intervention points for innovative therapeutic strategies in oncology. Public Library of Science 2015-11-03 /pmc/articles/PMC4631357/ /pubmed/26528548 http://dx.doi.org/10.1371/journal.pcbi.1004571 Text en © 2015 Cohen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cohen, David P. A.
Martignetti, Loredana
Robine, Sylvie
Barillot, Emmanuel
Zinovyev, Andrei
Calzone, Laurence
Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration
title Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration
title_full Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration
title_fullStr Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration
title_full_unstemmed Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration
title_short Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration
title_sort mathematical modelling of molecular pathways enabling tumour cell invasion and migration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631357/
https://www.ncbi.nlm.nih.gov/pubmed/26528548
http://dx.doi.org/10.1371/journal.pcbi.1004571
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