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Computational systems-biology approaches for modeling gene networks driving epithelial-mesenchymal transitions.

作者信息

Katebi Ataur, Ramirez Daniel, Lu Mingyang

机构信息

Department of Bioengineering, Northeastern University, Boston, Massachusetts, USA.

Center for Theoretical Biological Physics, Northeastern University, Boston, Massachusetts, USA.

出版信息

Comput Syst Oncol. 2021 Jun;1(2). doi: 10.1002/cso2.1021. Epub 2021 Jun 9.


DOI:10.1002/cso2.1021
PMID:34164628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8219219/
Abstract

Epithelial-mesenchymal transition (EMT) is an important biological process through which epithelial cells undergo phenotypic transitions to mesenchymal cells by losing cell-cell adhesion and gaining migratory properties that cells use in embryogenesis, wound healing, and cancer metastasis. An important research topic is to identify the underlying gene regulatory networks (GRNs) governing the decision making of EMT and develop predictive models based on the GRNs. The advent of recent genomic technology, such as single-cell RNA sequencing, has opened new opportunities to improve our understanding about the dynamical controls of EMT. In this article, we review three major types of computational and mathematical approaches and methods for inferring and modeling GRNs driving EMT. We emphasize (1) the bottom-up approaches, where GRNs are constructed through literature search; (2) the top-down approaches, where GRNs are derived from genome-wide sequencing data; (3) the combined top-down and bottom-up approaches, where EMT GRNs are constructed and simulated by integrating bioinformatics and mathematical modeling. We discuss the methodologies and applications of each approach and the available resources for these studies.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c19c/8219219/449c52390a48/nihms-1715391-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c19c/8219219/449c52390a48/nihms-1715391-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c19c/8219219/449c52390a48/nihms-1715391-f0001.jpg

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[1]
Computational systems-biology approaches for modeling gene networks driving epithelial-mesenchymal transitions.

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[2]
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[3]
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本文引用的文献

[1]
Network inference with Granger causality ensembles on single-cell transcriptomics.

Cell Rep. 2022-2-8

[2]
The role of mechanical interactions in EMT.

Phys Biol. 2021-5-12

[3]
Systems biology approach suggests new miRNAs as phenotypic stability factors in the epithelial-mesenchymal transition.

J R Soc Interface. 2020-10

[4]
NFATc Acts as a Non-Canonical Phenotypic Stability Factor for a Hybrid Epithelial/Mesenchymal Phenotype.

Front Oncol. 2020-9-8

[5]
Inference and multiscale model of epithelial-to-mesenchymal transition via single-cell transcriptomic data.

Nucleic Acids Res. 2020-9-25

[6]
Single-cell RNA sequencing reveals profibrotic roles of distinct epithelial and mesenchymal lineages in pulmonary fibrosis.

Sci Adv. 2020-7

[7]
Robust gene expression programs underlie recurrent cell states and phenotype switching in melanoma.

Nat Cell Biol. 2020-8-3

[8]
Identifying inhibitors of epithelial-mesenchymal plasticity using a network topology-based approach.

NPJ Syst Biol Appl. 2020-5-18

[9]
Toward Modeling Context-Specific EMT Regulatory Networks Using Temporal Single Cell RNA-Seq Data.

Front Mol Biosci. 2020-4-23

[10]
Context specificity of the EMT transcriptional response.

Nat Commun. 2020-5-1

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