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Modelling signalling networks from perturbation data.

Mathurin Dorel ,
Bertram Klinger ,
Torsten Gross ,
Anja Sieber ,
Anirudh Prahallad ,
Evert Bosdriesz ,
Lodewyk F A Wessels ,
Nils Blüthgen

Abstract

RESULTS

We developed the software package STASNet (STeady-STate Analysis of Signalling Networks) that provides an augmented and extended version of MRA suited to model signalling networks from incomplete perturbation schemes and multi-perturbation data. Using data from the Dialogue on Reverse Engineering Assessment and Methods challenge, we show that predictions from STASNet models are among the top-performing methods. We applied the method to study the effect of SHP2, a protein that has been implicated in resistance to targeted therapy in colon cancer, using a novel dataset from the colon cancer cell line Widr and a SHP2-depleted derivative. We find that SHP2 is required for mitogen-activated protein kinase signalling, whereas AKT signalling only partially depends on SHP2.

SUPPLEMENTARY INFORMATION

Supplementary data are available at Bioinformatics online.

MOTIVATION

Intracellular signalling is realized by complex signalling networks, which are almost impossible to understand without network models, especially if feedbacks are involved. Modular Response Analysis (MRA) is a convenient modelling method to study signalling networks in various contexts.

AVAILABILITY AND IMPLEMENTATION

An R-package is available at https://github.com/molsysbio/STASNet.

More about this publication

Bioinformatics (Oxford, England)

Volume 34
Issue nr. 23
Pages 4079-4086
Publication date 01-12-2018

Full text links

Publisher website (DOI) 10.1093/bioinformatics/bty473
Europe PubMed Central 29931053
Pubmed 29931053

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