dc.contributor.author
Thobe, Kirsten
dc.contributor.author
Kuznia, Christina
dc.contributor.author
Sers, Christine
dc.contributor.author
Siebert, Heike
dc.date.accessioned
2018-11-07T12:16:46Z
dc.date.available
2018-11-07T12:16:46Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/23180
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-972
dc.description.abstract
Systems biology studies the structure and dynamics of biological systems using mathematical approaches. Bottom-up approaches create models from prior knowledge but usually cannot cope with uncertainty, whereas top-down approaches infer models directly from data using statistical methods but mostly neglect valuable known information from former studies. Here, we want to present a workflow that includes prior knowledge while allowing for uncertainty in the modeling process. We build not one but all possible models that arise from the uncertainty using logical modeling and subsequently filter for those models in agreement with data in a top-down manner. This approach enables us to investigate new and more complex biological research questions, however, the encoding in such a framework is often not obvious and thus not easily accessible for researcher from life sciences. To mitigate this problem, we formulate a pipeline with specific templates to address some research questions common in signaling network analysis. To illustrate the potential of this approach, we applied the pipeline to growth factor signaling processes in two renal cancer cell lines. These two cell lines originate from similar tissue, but surprisingly showed a very different behavior toward the cancer drug Sorafenib. Thus our aim was to explore differences between these cell lines regarding three sources of uncertainty in one analysis: possible targets of Sorafenib, crosstalk between involved pathways, and the effect of a mutation in mammalian target of Rapamycin (mTOR) in one of the cell lines. We were able to show that the model pools from the cell lines are disjoint, thus the discrepancies in behavior originate from differences in the cellular wiring. Also the mutation in mTOR is not affecting its activity in the pathway. The results on Sorafenib, while not fully clarifying the mechanisms involved, illustrate the potential of this analysis for generating new hypotheses.
en
dc.format.extent
15 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
systems biology
en
dc.subject
logical modeling
en
dc.subject
model checking
en
dc.subject
constraint based modeling
en
dc.subject
signaling pathways
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie
dc.title
Evaluating Uncertainty in Signaling Networks using Logical Modeling
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
1335
dcterms.bibliographicCitation.doi
10.3389/fphys.2018.01335
dcterms.bibliographicCitation.journaltitle
Frontiers in Physiology
dcterms.bibliographicCitation.volume
9
dcterms.bibliographicCitation.url
https://doi.org/10.3389/fphys.2018.01335
refubium.affiliation
Mathematik und Informatik
refubium.affiliation.other
Institut für Mathematik

refubium.funding
Frontiers
refubium.funding
Institutional Participation
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
1664-042X