Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen

dc.contributor.author
Menden, Michael P.
dc.contributor.author
AstraZeneca-Sanger Drug Combination DREAM Consortium
dc.contributor.author
Saez-Rodriguez, Julio
dc.date.issued
2019-09-05T15:58:12Z
dc.date.issued
2019-09-05T15:58:12Z
dc.date.issued
2019
dc.identifier
Menden MP, Wang D, Mason MJ, Szalai B, Bulusu KC1, Guan Y et al. Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen. Nat Commun. 2019;10(1):2674. DOI: 10.1038/s41467-019-09799-2
dc.identifier
2041-1723
dc.identifier
http://hdl.handle.net/10230/42248
dc.identifier
http://dx.doi.org/10.1038/s41467-019-09799-2
dc.description.abstract
The effectiveness of most cancer targeted therapies is short-lived. Tumors often develop resistance that might be overcome with drug combinations. However, the number of possible combinations is vast, necessitating data-driven approaches to find optimal patient-specific treatments. Here we report AstraZeneca's large drug combination dataset, consisting of 11,576 experiments from 910 combinations across 85 molecularly characterized cancer cell lines, and results of a DREAM Challenge to evaluate computational strategies for predicting synergistic drug pairs and biomarkers. 160 teams participated to provide a comprehensive methodological development and benchmarking. Winning methods incorporate prior knowledge of drug-target interactions. Synergy is predicted with an accuracy matching biological replicates for >60% of combinations. However, 20% of drug combinations are poorly predicted by all methods. Genomic rationale for synergy predictions are identified, including ADAM17 inhibitor antagonism when combined with PIK3CB/D inhibition contrasting to synergy when combined with other PI3K-pathway inhibitors in PIK3CA mutant cells.
dc.description.abstract
We thank the Genomics of Drug Sensitivity in Cancer and COSMIC teams at the Wellcome Trust Sanger Institute for help with the preparation of the molecular data, Denes Turei for help with Omnipath, and Katjusa Koler for help with matching drug names across combination screens. We thank AstraZeneca for funding and provision of data to the DREAM Consortium to run the challenge, and funding from the European Union Horizon 2020 research (under grant agreement No 668858 PrECISE to J.S.R.), the Joint Research Center for Computational Biomedicine (which is partially funded by Bayer AG) to J.S.R., National Institute for Health Research (NIHR) Sheffield Biomedical Research Center, Premium Postdoctoral Fellowship Program of the Hungarian Academy of Sciences. M.G lab is supported by Wellcome Trust (102696 and 206194).
dc.format
application/pdf
dc.format
application/pdf
dc.language
eng
dc.publisher
Nature Research
dc.relation
Nature Communications. 2019;10(1):2674
dc.relation
info:eu-repo/grantAgreement/EC/H2020/668858
dc.rights
© The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
dc.rights
http://creativecommons.org/licenses/by/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Cancer
dc.subject
High-throughput screening
dc.subject
Machine learning
dc.subject
Statistical methods
dc.subject
Systems biology
dc.title
Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)