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S100A4 and its role in metastasis – computational integration of data on biological networks
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. Univ Svizzera Italiana, Switzerland. (CCBG)ORCID iD: 0000-0002-6469-0296
Univ Svizzera Italiana, Switzerland ;Swiss Inst Bioinformat, Switzerland.
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. (CCBG)ORCID iD: 0000-0001-8696-3104
2015 (English)In: Molecular Biosystems, ISSN 1742-206X, E-ISSN 1742-2051, Vol. 11, 2238-2246 p.Article in journal (Refereed) Published
Abstract [en]

Characterising signal transduction networks is fundamental to our understanding of biology. However, redundancy and different types of feedback mechanisms make it difficult to understand how variations of the network components contribute to a biological process. In silico modelling of signalling interactions therefore becomes increasingly useful for the development of successful therapeutic approaches. Unfortunately, quantitative information cannot be obtained for all of the proteins or complexes that comprise the network, which limits the usability of computational models. We developed a flexible computational framework for the analysis of biological signalling networks. We demonstrate our approach by studying the mechanism of metastasis promotion by the S100A4 protein, and suggest therapeutic strategies. The advantage of the proposed method is that only limited information (interaction type between species) is required to set up a steady-state network model. This permits a straightforward integration of experimental information where the lack of details are compensated by efficient sampling of the parameter space. We investigated regulatory properties of the S100A4 network and the role of different key components. The results show that S100A4 enhances the activity of matrix metalloproteinases (MMPs), causing higher cell dissociation. Moreover, it leads to an increased stability of the pathological state. Thus, avoiding metastasis in S100A4-expressing tumours requires multiple target inhibition. Moreover, the analysis could explain the previous failure of MMP inhibitors in clinical trials. Finally, our method is applicable to a wide range of biological questions that can be represented as directional networks.

Place, publisher, year, edition, pages
2015. Vol. 11, 2238-2246 p.
National Category
Bioinformatics and Systems Biology
Research subject
Natural Science, Biomedical Sciences
Identifiers
URN: urn:nbn:se:lnu:diva-45623DOI: 10.1039/c5mb00110bISI: 000358024000014Scopus ID: 2-s2.0-84951778100OAI: oai:DiVA.org:lnu-45623DiVA: diva2:844361
Available from: 2015-08-05 Created: 2015-08-05 Last updated: 2017-12-04Bibliographically approved

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