Deciphering epithelial-Mesenchymal Transition Regulatory Networks in Cancer through Computational Approaches

被引:39
作者
Burger, Gerhard A. [1 ]
Danen, Erik H. J. [1 ]
Beltman, Joost B. [1 ]
机构
[1] Leiden Univ, Leiden Acad Ctr Drug Res, Drug Discovery & Safety, Leiden, Netherlands
来源
FRONTIERS IN ONCOLOGY | 2017年 / 7卷
关键词
epithelial-mesenchymal transition; computational modeling; cancer progression; cell migration; stemness; cell metabolism; POSITIVE FEEDBACK LOOP; TGF-BETA; EMT PROGRAMS; TUMOR-CELLS; STEM-CELLS; METASTASIS; PLASTICITY; MIGRATION; PATHWAY; MODELS;
D O I
10.3389/fonc.2017.00162
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epithelial-mesenchymal transition (EMT), the process by which epithelial cells can convert into motile mesenchymal cells, plays an important role in development and wound healing but is also involved in cancer progression. It is increasingly recognized that EMT is a dynamic process involving multiple intermediate or "hybrid" phenotypes rather than an "all-or-none" process. However, the role of EMT in various cancer hallmarks, including metastasis, is debated. Given the complexity of EMT regulation, computational modeling has proven to be an invaluable tool for cancer research, i.e., to resolve apparent conflicts in experimental data and to guide experiments by generating testable hypotheses. In this review, we provide an overview of computational modeling efforts that have been applied to regulation of EMT in the context of cancer progression and its associated tumor characteristics. Moreover, we identify possibilities to bridge different modeling approaches and point out outstanding questions in which computational modeling can contribute to advance our understanding of pathological EMT.
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页数:14
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