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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
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.
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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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