High-throughput cancer hypothesis testing with an integrated PhysiCell-EMEWS workflow

dc.contributor.authorOzik, Jonathan
dc.contributor.authorCollier, Nicholson
dc.contributor.authorWozniak, Justin
dc.contributor.authorMacal, Charles
dc.contributor.authorCockrell, Chase
dc.contributor.authorFriedman, Samuel
dc.contributor.authorGhaffarizadeh, Ahmadreza
dc.contributor.authorHeiland, Randy
dc.contributor.authorMacklin, Paul
dc.date.accessioned2025-02-20T15:52:03Z
dc.date.available2025-02-20T15:52:03Z
dc.date.issued2018-12-21
dc.description.abstractBackground Cancer is a complex, multiscale dynamical system, with interactions between tumor cells and non-cancerous host systems. Therapies act on this combined cancer-host system, sometimes with unexpected results. Systematic investigation of mechanistic computational models can augment traditional laboratory and clinical studies, helping identify the factors driving a treatment’s success or failure. However, given the uncertainties regarding the underlying biology, these multiscale computational models can take many potential forms, in addition to encompassing high-dimensional parameter spaces. Therefore, the exploration of these models is computationally challenging. We propose that integrating two existing technologies—one to aid the construction of multiscale agent-based models, the other developed to enhance model exploration and optimization—can provide a computational means for high-throughput hypothesis testing, and eventually, optimization. Results In this paper, we introduce a high throughput computing (HTC) framework that integrates a mechanistic 3-D multicellular simulator (PhysiCell) with an extreme-scale model exploration platform (EMEWS) to investigate high-dimensional parameter spaces. We show early results in applying PhysiCell-EMEWS to 3-D cancer immunotherapy and show insights on therapeutic failure. We describe a generalized PhysiCell-EMEWS workflow for high-throughput cancer hypothesis testing, where hundreds or thousands of mechanistic simulations are compared against data-driven error metrics to perform hypothesis optimization. Conclusions While key notational and computational challenges remain, mechanistic agent-based models and high-throughput model exploration environments can be combined to systematically and rapidly explore key problems in cancer. These high-throughput computational experiments can improve our understanding of the underlying biology, drive future experiments, and ultimately inform clinical practice.
dc.identifier.citationOzik, Jonathan, et al. "High-throughput cancer hypothesis testing with an integrated PhysiCell-EMEWS workflow." BMC Bioinformatics, vol. 19, no. Suppl 18, pp. 82-97, 2018-12-21, https://doi.org/10.1186/s12859-018-2510-x.
dc.identifier.otherBRITE 3127
dc.identifier.urihttps://hdl.handle.net/2022/30414
dc.language.isoen
dc.relation.isversionofhttps://doi.org/10.1186/s12859-018-2510-x
dc.relation.isversionofhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302449
dc.relation.journalBMC Bioinformatics
dc.titleHigh-throughput cancer hypothesis testing with an integrated PhysiCell-EMEWS workflow

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