Cargando…
Additive Dose Response Models: Defining Synergy
In synergy studies, one focuses on compound combinations that promise a synergistic or antagonistic effect. With the help of high-throughput techniques, a huge amount of compound combinations can be screened and filtered for suitable candidates for a more detailed analysis. Those promising candidate...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901947/ https://www.ncbi.nlm.nih.gov/pubmed/31849651 http://dx.doi.org/10.3389/fphar.2019.01384 |
_version_ | 1783477589896069120 |
---|---|
author | Lederer, Simone Dijkstra, Tjeerd M. H. Heskes, Tom |
author_facet | Lederer, Simone Dijkstra, Tjeerd M. H. Heskes, Tom |
author_sort | Lederer, Simone |
collection | PubMed |
description | In synergy studies, one focuses on compound combinations that promise a synergistic or antagonistic effect. With the help of high-throughput techniques, a huge amount of compound combinations can be screened and filtered for suitable candidates for a more detailed analysis. Those promising candidates are chosen based on the deviance between a measured response and an expected non-interactive response. A non-interactive response is based on a principle of no interaction, such as Loewe Additivity or Bliss Independence. In a previous study, we introduced, an explicit formulation of the hitherto implicitly defined Loewe Additivity, the so-called Explicit Mean Equation. In the current study we show that this Explicit Mean Equation outperforms the original implicit formulation of Loewe Additivity and Bliss Independence when measuring synergy in terms of the deviance between measured and expected response, called the lack-of-fit. Further, we show that computing synergy as lack-of-fit outperforms a parametric approach. We show this on two datasets of compound combinations that are categorized into synergistic, non-interactive, and antagonistic. |
format | Online Article Text |
id | pubmed-6901947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69019472019-12-17 Additive Dose Response Models: Defining Synergy Lederer, Simone Dijkstra, Tjeerd M. H. Heskes, Tom Front Pharmacol Pharmacology In synergy studies, one focuses on compound combinations that promise a synergistic or antagonistic effect. With the help of high-throughput techniques, a huge amount of compound combinations can be screened and filtered for suitable candidates for a more detailed analysis. Those promising candidates are chosen based on the deviance between a measured response and an expected non-interactive response. A non-interactive response is based on a principle of no interaction, such as Loewe Additivity or Bliss Independence. In a previous study, we introduced, an explicit formulation of the hitherto implicitly defined Loewe Additivity, the so-called Explicit Mean Equation. In the current study we show that this Explicit Mean Equation outperforms the original implicit formulation of Loewe Additivity and Bliss Independence when measuring synergy in terms of the deviance between measured and expected response, called the lack-of-fit. Further, we show that computing synergy as lack-of-fit outperforms a parametric approach. We show this on two datasets of compound combinations that are categorized into synergistic, non-interactive, and antagonistic. Frontiers Media S.A. 2019-11-26 /pmc/articles/PMC6901947/ /pubmed/31849651 http://dx.doi.org/10.3389/fphar.2019.01384 Text en Copyright © 2019 Lederer, Dijkstra and Heskes http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Lederer, Simone Dijkstra, Tjeerd M. H. Heskes, Tom Additive Dose Response Models: Defining Synergy |
title | Additive Dose Response Models: Defining Synergy |
title_full | Additive Dose Response Models: Defining Synergy |
title_fullStr | Additive Dose Response Models: Defining Synergy |
title_full_unstemmed | Additive Dose Response Models: Defining Synergy |
title_short | Additive Dose Response Models: Defining Synergy |
title_sort | additive dose response models: defining synergy |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901947/ https://www.ncbi.nlm.nih.gov/pubmed/31849651 http://dx.doi.org/10.3389/fphar.2019.01384 |
work_keys_str_mv | AT lederersimone additivedoseresponsemodelsdefiningsynergy AT dijkstratjeerdmh additivedoseresponsemodelsdefiningsynergy AT heskestom additivedoseresponsemodelsdefiningsynergy |