Optimization of drug combinations using Feedback System Control
Nowak-Sliwinska et al . describe a protocol for optimizing drug combinations using Feedback System Control (FSC). Drug combinations are tested in a cell-based assay in which results are entered into the FSC pipeline to predict new combinations to be tested in vitro . We describe a protocol for the d...
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| Published in | Nature protocols Vol. 11; no. 2; pp. 302 - 315 |
|---|---|
| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
Nature Publishing Group UK
01.02.2016
Nature Publishing Group |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1754-2189 1750-2799 1750-2799 |
| DOI | 10.1038/nprot.2016.017 |
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| Abstract | Nowak-Sliwinska
et al
. describe a protocol for optimizing drug combinations using Feedback System Control (FSC). Drug combinations are tested in a cell-based assay in which results are entered into the FSC pipeline to predict new combinations to be tested
in vitro
.
We describe a protocol for the discovery of synergistic drug combinations for the treatment of disease. Synergistic drug combinations lead to the use of drugs at lower doses, which reduces side effects and can potentially lead to reduced drug resistance, while being clinically more effective than the individual drugs. To cope with the extremely large search space for these combinations, we developed an efficient combinatorial drug screening method called the Feedback System Control (FSC) technique. Starting with a broad selection of drugs, the method follows an iterative approach of experimental testing in a relevant bioassay and analysis of the results by FSC. First, the protocol uses a cell viability assay to generate broad dose-response curves to assess the efficacy of individual compounds. These curves are then used to guide the dosage input of each drug to be tested in combination. Data from applied drug combinations are input into the differential evolution (DE) algorithm, which predicts new combinations to be tested
in vitro
. This process identifies optimal drug-dose combinations, while saving orders of magnitude in experimental effort. The complete optimization process is estimated to take ∼4 weeks. FSC does not require insight into the disease mechanism, and it has therefore been applied to find combination therapies for many different pathologies, including cancer and infectious diseases, and it has also been used in organ transplantation. |
|---|---|
| AbstractList | We describe a protocol for the discovery of synergistic drug combinations for the treatment of disease. Synergistic drug combinations lead to the use of drugs at lower doses, which reduces side effects and can potentially lead to reduced drug resistance, while being clinically more effective than the individual drugs. To cope with the extremely large search space for these combinations, we developed an efficient combinatorial drug screening method called the Feedback System Control (FSC) technique. Starting with a broad selection of drugs, the method follows an iterative approach of experimental testing in a relevant bioassay and analysis of the results by FSC. First, the protocol uses a cell viability assay to generate broad dose-response curves to assess the efficacy of individual compounds. These curves are then used to guide the dosage input of each drug to be tested in combination. Data from applied drug combinations are input into the differential evolution (DE) algorithm, which predicts new combinations to be tested in vitro. This process identifies optimal drug-dose combinations, while saving orders of magnitude in experimental effort. The complete optimization process is estimated to take ∼4 weeks. FSC does not require insight into the disease mechanism, and it has therefore been applied to find combination therapies for many different pathologies, including cancer and infectious diseases, and it has also been used in organ transplantation.We describe a protocol for the discovery of synergistic drug combinations for the treatment of disease. Synergistic drug combinations lead to the use of drugs at lower doses, which reduces side effects and can potentially lead to reduced drug resistance, while being clinically more effective than the individual drugs. To cope with the extremely large search space for these combinations, we developed an efficient combinatorial drug screening method called the Feedback System Control (FSC) technique. Starting with a broad selection of drugs, the method follows an iterative approach of experimental testing in a relevant bioassay and analysis of the results by FSC. First, the protocol uses a cell viability assay to generate broad dose-response curves to assess the efficacy of individual compounds. These curves are then used to guide the dosage input of each drug to be tested in combination. Data from applied drug combinations are input into the differential evolution (DE) algorithm, which predicts new combinations to be tested in vitro. This process identifies optimal drug-dose combinations, while saving orders of magnitude in experimental effort. The complete optimization process is estimated to take ∼4 weeks. FSC does not require insight into the disease mechanism, and it has therefore been applied to find combination therapies for many different pathologies, including cancer and infectious diseases, and it has also been used in organ transplantation. Nowak-Sliwinska et al. describe a protocol for optimizing drug combinations using Feedback System Control (FSC). Drug combinations are tested in a cell-based assay in which results are entered into the FSC pipeline to predict new combinations to be tested in vitro.We describe a protocol for the discovery of synergistic drug combinations for the treatment of disease. Synergistic drug combinations lead to the use of drugs at lower doses, which reduces side effects and can potentially lead to reduced drug resistance, while being clinically more effective than the individual drugs. To cope with the extremely large search space for these combinations, we developed an efficient combinatorial drug screening method called the Feedback System Control (FSC) technique. Starting with a broad selection of drugs, the method follows an iterative approach of experimental testing in a relevant bioassay and analysis of the results by FSC. First, the protocol uses a cell viability assay to generate broad dose-response curves to assess the efficacy of individual compounds. These curves are then used to guide the dosage input of each drug to be tested in combination. Data from applied drug combinations are input into the differential evolution (DE) algorithm, which predicts new combinations to be tested in vitro. This process identifies optimal drug-dose combinations, while saving orders of magnitude in experimental effort. The complete optimization process is estimated to take ∼4 weeks. FSC does not require insight into the disease mechanism, and it has therefore been applied to find combination therapies for many different pathologies, including cancer and infectious diseases, and it has also been used in organ transplantation. Nowak-Sliwinska et al . describe a protocol for optimizing drug combinations using Feedback System Control (FSC). Drug combinations are tested in a cell-based assay in which results are entered into the FSC pipeline to predict new combinations to be tested in vitro . We describe a protocol for the discovery of synergistic drug combinations for the treatment of disease. Synergistic drug combinations lead to the use of drugs at lower doses, which reduces side effects and can potentially lead to reduced drug resistance, while being clinically more effective than the individual drugs. To cope with the extremely large search space for these combinations, we developed an efficient combinatorial drug screening method called the Feedback System Control (FSC) technique. Starting with a broad selection of drugs, the method follows an iterative approach of experimental testing in a relevant bioassay and analysis of the results by FSC. First, the protocol uses a cell viability assay to generate broad dose-response curves to assess the efficacy of individual compounds. These curves are then used to guide the dosage input of each drug to be tested in combination. Data from applied drug combinations are input into the differential evolution (DE) algorithm, which predicts new combinations to be tested in vitro . This process identifies optimal drug-dose combinations, while saving orders of magnitude in experimental effort. The complete optimization process is estimated to take ∼4 weeks. FSC does not require insight into the disease mechanism, and it has therefore been applied to find combination therapies for many different pathologies, including cancer and infectious diseases, and it has also been used in organ transplantation. We describe a protocol for the discovery of synergistic drug combinations for the treatment of disease. Synergistic drug combinations lead to the use of drugs at lower doses, which reduces side effects and can potentially lead to reduced drug resistance, while being clinically more effective than the individual drugs. To cope with the extremely large search space for these combinations, we developed an efficient combinatorial drug screening method called the Feedback System Control (FSC) technique. Starting with a broad selection of drugs, the method follows an iterative approach of experimental testing in a relevant bioassay and analysis of the results by FSC. First, the protocol uses a cell viability assay to generate broad dose-response curves to assess the efficacy of individual compounds. These curves are then used to guide the dosage input of each drug to be tested in combination. Data from applied drug combinations are input into the differential evolution (DE) algorithm, which predicts new combinations to be tested in vitro. This process identifies optimal drug-dose combinations, while saving orders of magnitude in experimental effort. The complete optimization process is estimated to take ∼4 weeks. FSC does not require insight into the disease mechanism, and it has therefore been applied to find combination therapies for many different pathologies, including cancer and infectious diseases, and it has also been used in organ transplantation. We describe a protocol for the discovery of synergistic drug combinations for the treatment of disease. Synergistic drug combinations lead to the use of drugs at lower doses, which reduces side effects and can potentially lead to reduced drug resistance, while being clinically more effective than the individual drugs. To cope with the extremely large search space for these combinations, we developed an efficient combinatorial drug screening method called the Feedback system control (FSC) technique. starting with a broad selection of drugs, the method follows an iterative approach of experimental testing in a relevant bioassay and analysis of the results by FSC. First, the protocol uses a cell viability assay to generate broad dose- response curves to assess the efficacy of individual compounds. these curves are then used to guide the dosage input of each drug to be tested in combination. Data from applied drug combinations are input into the differential evolution (DE) algorithm, which predicts new combinations to be tested in vitro. this process identifies optimal drug-dose combinations, while saving orders of magnitude in experimental effort. the complete optimization process is estimated to take ~4 weeks. FSC does not require insight into the disease mechanism, and it has therefore been applied to find combination therapies for many different pathologies, including cancer and infectious diseases, and it has also been used in organ transplantation. |
| Audience | Academic |
| Author | Ding, Xianting van den Bergh, Hubert Ho, Chih-Ming Griffioen, Arjan W Nowak-Sliwinska, Patrycja Dyson, Paul J Weiss, Andrea |
| Author_xml | – sequence: 1 givenname: Patrycja surname: Nowak-Sliwinska fullname: Nowak-Sliwinska, Patrycja email: p.nowak-sliwinska@vumc.nl organization: Department of Medical Oncology, Angiogenesis Laboratory, Vrije Universiteit (VU) University Medical Center – sequence: 2 givenname: Andrea surname: Weiss fullname: Weiss, Andrea organization: Department of Medical Oncology, Angiogenesis Laboratory, Vrije Universiteit (VU) University Medical Center – sequence: 3 givenname: Xianting surname: Ding fullname: Ding, Xianting organization: Med-X Research Institute, School of Biomedical Engineering, Shanghai Jiao Tong University – sequence: 4 givenname: Paul J surname: Dyson fullname: Dyson, Paul J organization: Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology Lausanne (EPFL) – sequence: 5 givenname: Hubert surname: van den Bergh fullname: van den Bergh, Hubert organization: Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology Lausanne (EPFL) – sequence: 6 givenname: Arjan W surname: Griffioen fullname: Griffioen, Arjan W organization: Department of Medical Oncology, Angiogenesis Laboratory, Vrije Universiteit (VU) University Medical Center – sequence: 7 givenname: Chih-Ming orcidid: 0000-0001-7369-5446 surname: Ho fullname: Ho, Chih-Ming email: chihming@g.ucla.edu organization: Department of Mechanical and Aerospace Engineering, University of California |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26766116$$D View this record in MEDLINE/PubMed |
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| Snippet | Nowak-Sliwinska
et al
. describe a protocol for optimizing drug combinations using Feedback System Control (FSC). Drug combinations are tested in a cell-based... We describe a protocol for the discovery of synergistic drug combinations for the treatment of disease. Synergistic drug combinations lead to the use of drugs... Nowak-Sliwinska et al. describe a protocol for optimizing drug combinations using Feedback System Control (FSC). Drug combinations are tested in a cell-based... |
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| SubjectTerms | 631/114/2415 631/154/1435 631/1647/2163 631/1647/794 Algorithms Analytical Chemistry Bioassays Biological Assay Biological Techniques Cancer Cell viability Combinatorial analysis Computational Biology/Bioinformatics Control systems Disease Drug Combinations Drug dosages Drug Evaluation, Preclinical - methods Drug resistance Drug screening Drug Synergism Drug therapy, Combination Drug Therapy, Combination - methods Drugs Evolutionary algorithms Evolutionary computation Feedback Humans Immunosuppressive agents Infectious diseases Input output analysis Life Sciences Medical treatment Methods Microarrays Observations Optimization Organic Chemistry Pharmacology, Experimental Protocol Side effects Transplantation |
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| Title | Optimization of drug combinations using Feedback System Control |
| URI | https://link.springer.com/article/10.1038/nprot.2016.017 https://www.ncbi.nlm.nih.gov/pubmed/26766116 https://www.proquest.com/docview/1757042931 https://www.proquest.com/docview/2564691836 https://www.proquest.com/docview/1760894685 http://infoscience.epfl.ch/record/217805 |
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