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Zhang, F |
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Zhang, P |
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Zhang, W |
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Zhao, H |
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Zhao, L |
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Zheng, W |
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Zoufir, A |
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dc.contributor.author |
Zucknick, M |
|
dc.contributor.author |
AstraZeneca-Sanger, Drug Combination DREAM Consortium |
|
dc.contributor.author |
Jang, IS |
|
dc.contributor.author |
Ghazoui, Z |
|
dc.contributor.author |
Ahsen, ME |
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dc.contributor.author |
Vogel, R |
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dc.contributor.author |
Neto, EC |
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dc.contributor.author |
Norman, T |
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dc.contributor.author |
Tang, EKY |
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dc.contributor.author |
Garnett, MJ |
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dc.contributor.author |
Veroli, GYD |
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dc.contributor.author |
Fawell, S |
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dc.contributor.author |
Stolovitzky, G |
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Guinney, J |
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dc.contributor.author |
Dry, JR |
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dc.contributor.author |
Saez-Rodriguez, J |
|
dc.date.accessioned |
2020-09-18T09:25:57Z |
|
dc.date.available |
2020-09-18T09:25:57Z |
|
dc.date.issued |
2019 |
|
dc.identifier |
85067453487 |
|
dc.identifier.citation |
journalVolume=10;journalIssueNumber=1;pagination=2674, pages: 17;journalTitle=NATURE COMMUNICATIONS;journalAbbreviatedTitle=NAT COMMUN; |
|
dc.identifier.uri |
http://repo.lib.semmelweis.hu//handle/123456789/8007 |
|
dc.identifier.uri |
doi: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. © 2019, The Author(s). |
|
dc.relation.ispartof |
urn:issn:2041-1723 |
|
dc.title |
Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen |
|
dc.type |
Journal Article |
|
dc.date.updated |
2019-11-25T14:52:43Z |
|
dc.language.rfc3066 |
en |
|
dc.rights.holder |
NULL |
|
dc.identifier.mtmt |
30791492 |
|
dc.identifier.wos |
000471758500010 |
|
dc.identifier.pubmed |
31209238 |
|
dc.contributor.department |
SE/AOK/I/Élettani Intézet |
|
dc.contributor.department |
SE/AOK/I/ÉI/MTA-SE Molekuláris Élettani Kutatócsoport |
|
dc.contributor.institution |
Semmelweis Egyetem |
|