Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration

被引:86
|
作者
Cohen, David P. A. [1 ,2 ,3 ]
Martignetti, Loredana [1 ,2 ,3 ]
Robine, Sylvie [1 ,4 ]
Barillot, Emmanuel [1 ,2 ,3 ]
Zinovyev, Andrei [1 ,2 ,3 ]
Calzone, Laurence [1 ,2 ,3 ]
机构
[1] Inst Curie, Paris, France
[2] INSERM, U900, Paris, France
[3] Mines ParisTech, Paris, France
[4] CNRS UMR144, Paris, France
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; E-CADHERIN EXPRESSION; GENE SET ENRICHMENT; BREAST-CANCER CELLS; GROWTH-FACTOR-BETA; BODY-MASS INDEX; DOWN-REGULATION; AKT ISOFORMS; PHYSICAL-ACTIVITY; CATENIN;
D O I
10.1371/journal.pcbi.1004571
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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-beta-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.
引用
收藏
页数:29
相关论文
共 50 条
  • [1] The mathematical modelling of tumour angiogenesis and invasion
    Chaplain, MAJ
    ACTA BIOTHEORETICA, 1995, 43 (04) : 387 - 402
  • [2] Mathematical modelling of cell migration
    Butler, George
    Rudge, Jonathan
    Dash, Philip R.
    MECHANISMS OF CELL MIGRATION, 2019, 63 (05): : 631 - 637
  • [3] Mathematical modelling of cancer invasion: Implications of cell adhesion variability for tumour infiltrative growth patterns
    Domschke, Pia
    Trucu, Dumitru
    Gerisch, Alf
    Chaplain, Mark A. J.
    JOURNAL OF THEORETICAL BIOLOGY, 2014, 361 : 41 - 60
  • [4] Mathematical modelling of cancer cell invasion of tissue
    Ramis-Conde, Ignacio
    Chaplain, Mark A. J.
    Anderson, Alexander R. A.
    MATHEMATICAL AND COMPUTER MODELLING, 2008, 47 (5-6) : 533 - 545
  • [5] Ion channels and transporters in tumour cell migration and invasion
    Schwab, Albrecht
    Stock, Christian
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2014, 369 (1638)
  • [6] Mathematical modelling of cancer invasion: The multiple roles of TGF-β pathway on tumour proliferation and cell adhesion
    Bitsouni, Vasiliki
    Chaplain, Mark A. J.
    Eftimie, Raluca
    MATHEMATICAL MODELS & METHODS IN APPLIED SCIENCES, 2017, 27 (10): : 1929 - 1962
  • [7] THE MACROPHAGE MIGRATION ACTIVITY IS REQUIRED FOR TUMOUR CELL INVASION
    Guiet, R.
    Van Goethem, E.
    Cougoule, C.
    Balor, S.
    Valette, A.
    Lowell, C. A.
    Le Cabec, V.
    Maridonneau-Parini, I.
    INFLAMMATION RESEARCH, 2011, 60 : 46 - 47
  • [8] Role of PKN isoforms in tumour cell migration/invasion
    Lachmann, S.
    Jevons, A.
    Parker, P. J.
    FEBS JOURNAL, 2007, 274 : 356 - 356
  • [9] From passive diffusion to active cellular migration in mathematical models of tumour invasion
    Tracqui, P
    ACTA BIOTHEORETICA, 1995, 43 (04) : 443 - 464
  • [10] Mathematical modelling of proteolysis and cancer cell invasion of tissue
    Lolas, Georgios
    TUTORIALS IN MATHEMATICAL BIOSCIENCES III: CELL CYCLE, PROLIFERATION, AND CANCER, 2006, 1872 : 77 - 129