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Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen
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 As...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572829/ https://www.ncbi.nlm.nih.gov/pubmed/31209238 http://dx.doi.org/10.1038/s41467-019-09799-2 |
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author | Menden, Michael P. Wang, Dennis Mason, Mike J. Szalai, Bence Bulusu, Krishna C. Guan, Yuanfang Yu, Thomas Kang, Jaewoo Jeon, Minji Wolfinger, Russ Nguyen, Tin Zaslavskiy, Mikhail Jang, In Sock Ghazoui, Zara Ahsen, Mehmet Eren Vogel, Robert Neto, Elias Chaibub Norman, Thea Tang, Eric K. Y. Garnett, Mathew J. Veroli, Giovanni Y. Di Fawell, Stephen Stolovitzky, Gustavo Guinney, Justin Dry, Jonathan R. Saez-Rodriguez, Julio |
author_facet | Menden, Michael P. Wang, Dennis Mason, Mike J. Szalai, Bence Bulusu, Krishna C. Guan, Yuanfang Yu, Thomas Kang, Jaewoo Jeon, Minji Wolfinger, Russ Nguyen, Tin Zaslavskiy, Mikhail Jang, In Sock Ghazoui, Zara Ahsen, Mehmet Eren Vogel, Robert Neto, Elias Chaibub Norman, Thea Tang, Eric K. Y. Garnett, Mathew J. Veroli, Giovanni Y. Di Fawell, Stephen Stolovitzky, Gustavo Guinney, Justin Dry, Jonathan R. Saez-Rodriguez, Julio |
author_sort | Menden, Michael P. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6572829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65728292019-06-24 Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen Menden, Michael P. Wang, Dennis Mason, Mike J. Szalai, Bence Bulusu, Krishna C. Guan, Yuanfang Yu, Thomas Kang, Jaewoo Jeon, Minji Wolfinger, Russ Nguyen, Tin Zaslavskiy, Mikhail Jang, In Sock Ghazoui, Zara Ahsen, Mehmet Eren Vogel, Robert Neto, Elias Chaibub Norman, Thea Tang, Eric K. Y. Garnett, Mathew J. Veroli, Giovanni Y. Di Fawell, Stephen Stolovitzky, Gustavo Guinney, Justin Dry, Jonathan R. Saez-Rodriguez, Julio Nat Commun Article 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. Nature Publishing Group UK 2019-06-17 /pmc/articles/PMC6572829/ /pubmed/31209238 http://dx.doi.org/10.1038/s41467-019-09799-2 Text en © 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/. |
spellingShingle | Article Menden, Michael P. Wang, Dennis Mason, Mike J. Szalai, Bence Bulusu, Krishna C. Guan, Yuanfang Yu, Thomas Kang, Jaewoo Jeon, Minji Wolfinger, Russ Nguyen, Tin Zaslavskiy, Mikhail Jang, In Sock Ghazoui, Zara Ahsen, Mehmet Eren Vogel, Robert Neto, Elias Chaibub Norman, Thea Tang, Eric K. Y. Garnett, Mathew J. Veroli, Giovanni Y. Di Fawell, Stephen Stolovitzky, Gustavo Guinney, Justin Dry, Jonathan R. Saez-Rodriguez, Julio Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen |
title | Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen |
title_full | Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen |
title_fullStr | Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen |
title_full_unstemmed | Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen |
title_short | Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen |
title_sort | community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572829/ https://www.ncbi.nlm.nih.gov/pubmed/31209238 http://dx.doi.org/10.1038/s41467-019-09799-2 |
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