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dc.contributor.authorBrown, James L
dc.contributor.authorShovman, Mark
dc.contributor.authorRobertson, Paul
dc.contributor.authorBoiko, Andrei
dc.contributor.authorGoltsov, Alexey
dc.contributor.authorMullen, Peter
dc.contributor.authorHarrison, David James
dc.date.accessioned2016-06-17T10:30:04Z
dc.date.available2016-06-17T10:30:04Z
dc.date.issued2017-05
dc.identifier241708602
dc.identifier05fbb48a-240b-4e91-87e3-8e851e75c2aa
dc.identifierPMC5444693
dc.identifier85018966444
dc.identifier000400456200010
dc.identifier.citationBrown , J L , Shovman , M , Robertson , P , Boiko , A , Goltsov , A , Mullen , P & Harrison , D J 2017 , ' A signaling visualization toolkit to support rational design of combination therapies and biomarker discovery : SiViT ' , Oncotarget , vol. 8 , no. 18 , pp. 29657-29667 . https://doi.org/10.18632/oncotarget.8747en
dc.identifier.issn1949-2553
dc.identifier.otherORCID: /0000-0001-9041-9988/work/64034330
dc.identifier.otherORCID: /0000-0002-0841-609X/work/157141013
dc.identifier.urihttps://hdl.handle.net/10023/9005
dc.description.abstractTargeted cancer therapy aims to disrupt aberrant cellular signalling pathways. Biomarkers are surrogates of pathway state, but there is limited success in translating candidate biomarkers to clinical practice due to the intrinsic complexity of pathway networks. Systems biology approaches afford better understanding of complex, dynamical interactions in signalling pathways targeted by anticancer drugs. However, adoption of dynamical modelling by clinicians and biologists is impeded by model inaccessibility. Drawing on computer games technology, we present a novel visualisation toolkit, SiViT, that converts systems biology models of cancer cell signalling into interactive simulations that can be used without specialist computational expertise. SiViT allows clinicians and biologists to directly introduce for example loss of function mutations and specific inhibitors. SiViT animates the effects of these introductions on pathway dynamics, suggesting further experiments and assessing candidate biomarker effectiveness. In a systems biology model of Her2 signalling we experimentally validated predictions using SiViT, revealing the dynamics of biomarkers of drug resistance and highlighting the role of pathway crosstalk. No model is ever complete: the iteration of real data and simulation facilitates continued evolution of more accurate, useful models. SiViT will make accessible libraries of models to support preclinical research, combinatorial strategy design and biomarker discovery.
dc.format.extent11
dc.format.extent4638588
dc.language.isoeng
dc.relation.ispartofOncotargeten
dc.subjectInteractive visualizationen
dc.subjectSystems biologyen
dc.subjectSignaling networksen
dc.subjectCombination therapyen
dc.subjectBiomarker discoveryen
dc.subjectRC0254 Neoplasms. Tumors. Oncology (including Cancer)en
dc.subjectNDASen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subject.lccRC0254en
dc.titleA signaling visualization toolkit to support rational design of combination therapies and biomarker discovery : SiViTen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Cellular Medicine Divisionen
dc.identifier.doi10.18632/oncotarget.8747
dc.description.statusPeer revieweden


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