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Quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies
We developed a systematic algorithmic solution for quantitative drug sensitivity scoring (DSS), based on continuous modeling and integration of multiple dose-response relationships in high-throughput compound testing studies. Mathematical model estimation and continuous interpolation makes the scori...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046135/ https://www.ncbi.nlm.nih.gov/pubmed/24898935 http://dx.doi.org/10.1038/srep05193 |
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author | Yadav, Bhagwan Pemovska, Tea Szwajda, Agnieszka Kulesskiy, Evgeny Kontro, Mika Karjalainen, Riikka Majumder, Muntasir Mamun Malani, Disha Murumägi, Astrid Knowles, Jonathan Porkka, Kimmo Heckman, Caroline Kallioniemi, Olli Wennerberg, Krister Aittokallio, Tero |
author_facet | Yadav, Bhagwan Pemovska, Tea Szwajda, Agnieszka Kulesskiy, Evgeny Kontro, Mika Karjalainen, Riikka Majumder, Muntasir Mamun Malani, Disha Murumägi, Astrid Knowles, Jonathan Porkka, Kimmo Heckman, Caroline Kallioniemi, Olli Wennerberg, Krister Aittokallio, Tero |
author_sort | Yadav, Bhagwan |
collection | PubMed |
description | We developed a systematic algorithmic solution for quantitative drug sensitivity scoring (DSS), based on continuous modeling and integration of multiple dose-response relationships in high-throughput compound testing studies. Mathematical model estimation and continuous interpolation makes the scoring approach robust against sources of technical variability and widely applicable to various experimental settings, both in cancer cell line models and primary patient-derived cells. Here, we demonstrate its improved performance over other response parameters especially in a leukemia patient case study, where differential DSS between patient and control cells enabled identification of both cancer-selective drugs and drug-sensitive patient sub-groups, as well as dynamic monitoring of the response patterns and oncogenic driver signals during cancer progression and relapse in individual patient cells ex vivo. An open-source and easily extendable implementation of the DSS calculation is made freely available to support its tailored application to translating drug sensitivity testing results into clinically actionable treatment options. |
format | Online Article Text |
id | pubmed-4046135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40461352014-06-12 Quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies Yadav, Bhagwan Pemovska, Tea Szwajda, Agnieszka Kulesskiy, Evgeny Kontro, Mika Karjalainen, Riikka Majumder, Muntasir Mamun Malani, Disha Murumägi, Astrid Knowles, Jonathan Porkka, Kimmo Heckman, Caroline Kallioniemi, Olli Wennerberg, Krister Aittokallio, Tero Sci Rep Article We developed a systematic algorithmic solution for quantitative drug sensitivity scoring (DSS), based on continuous modeling and integration of multiple dose-response relationships in high-throughput compound testing studies. Mathematical model estimation and continuous interpolation makes the scoring approach robust against sources of technical variability and widely applicable to various experimental settings, both in cancer cell line models and primary patient-derived cells. Here, we demonstrate its improved performance over other response parameters especially in a leukemia patient case study, where differential DSS between patient and control cells enabled identification of both cancer-selective drugs and drug-sensitive patient sub-groups, as well as dynamic monitoring of the response patterns and oncogenic driver signals during cancer progression and relapse in individual patient cells ex vivo. An open-source and easily extendable implementation of the DSS calculation is made freely available to support its tailored application to translating drug sensitivity testing results into clinically actionable treatment options. Nature Publishing Group 2014-06-05 /pmc/articles/PMC4046135/ /pubmed/24898935 http://dx.doi.org/10.1038/srep05193 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images in this article are included in the article's Creative Commons license, unless indicated otherwise in the image credit; if the image is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the image. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Article Yadav, Bhagwan Pemovska, Tea Szwajda, Agnieszka Kulesskiy, Evgeny Kontro, Mika Karjalainen, Riikka Majumder, Muntasir Mamun Malani, Disha Murumägi, Astrid Knowles, Jonathan Porkka, Kimmo Heckman, Caroline Kallioniemi, Olli Wennerberg, Krister Aittokallio, Tero Quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies |
title | Quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies |
title_full | Quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies |
title_fullStr | Quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies |
title_full_unstemmed | Quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies |
title_short | Quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies |
title_sort | quantitative scoring of differential drug sensitivity for individually optimized anticancer therapies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046135/ https://www.ncbi.nlm.nih.gov/pubmed/24898935 http://dx.doi.org/10.1038/srep05193 |
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