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Systems Chronotherapeutics

Chronotherapeutics aim at treating illnesses according to the endogenous biologic rhythms, which moderate xenobiotic metabolism and cellular drug response. The molecular clocks present in individual cells involve approximately fifteen clock genes interconnected in regulatory feedback loops. They are...

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Autores principales: Ballesta, Annabelle, Innominato, Pasquale F., Dallmann, Robert, Rand, David A., Lévi, Francis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Pharmacology and Experimental Therapeutics 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394920/
https://www.ncbi.nlm.nih.gov/pubmed/28351863
http://dx.doi.org/10.1124/pr.116.013441
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author Ballesta, Annabelle
Innominato, Pasquale F.
Dallmann, Robert
Rand, David A.
Lévi, Francis A.
author_facet Ballesta, Annabelle
Innominato, Pasquale F.
Dallmann, Robert
Rand, David A.
Lévi, Francis A.
author_sort Ballesta, Annabelle
collection PubMed
description Chronotherapeutics aim at treating illnesses according to the endogenous biologic rhythms, which moderate xenobiotic metabolism and cellular drug response. The molecular clocks present in individual cells involve approximately fifteen clock genes interconnected in regulatory feedback loops. They are coordinated by the suprachiasmatic nuclei, a hypothalamic pacemaker, which also adjusts the circadian rhythms to environmental cycles. As a result, many mechanisms of diseases and drug effects are controlled by the circadian timing system. Thus, the tolerability of nearly 500 medications varies by up to fivefold according to circadian scheduling, both in experimental models and/or patients. Moreover, treatment itself disrupted, maintained, or improved the circadian timing system as a function of drug timing. Improved patient outcomes on circadian-based treatments (chronotherapy) have been demonstrated in randomized clinical trials, especially for cancer and inflammatory diseases. However, recent technological advances have highlighted large interpatient differences in circadian functions resulting in significant variability in chronotherapy response. Such findings advocate for the advancement of personalized chronotherapeutics through interdisciplinary systems approaches. Thus, the combination of mathematical, statistical, technological, experimental, and clinical expertise is now shaping the development of dedicated devices and diagnostic and delivery algorithms enabling treatment individualization. In particular, multiscale systems chronopharmacology approaches currently combine mathematical modeling based on cellular and whole-body physiology to preclinical and clinical investigations toward the design of patient-tailored chronotherapies. We review recent systems research works aiming to the individualization of disease treatment, with emphasis on both cancer management and circadian timing system–resetting strategies for improving chronic disease control and patient outcomes.
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spelling pubmed-53949202017-05-02 Systems Chronotherapeutics Ballesta, Annabelle Innominato, Pasquale F. Dallmann, Robert Rand, David A. Lévi, Francis A. Pharmacol Rev Review Articles Chronotherapeutics aim at treating illnesses according to the endogenous biologic rhythms, which moderate xenobiotic metabolism and cellular drug response. The molecular clocks present in individual cells involve approximately fifteen clock genes interconnected in regulatory feedback loops. They are coordinated by the suprachiasmatic nuclei, a hypothalamic pacemaker, which also adjusts the circadian rhythms to environmental cycles. As a result, many mechanisms of diseases and drug effects are controlled by the circadian timing system. Thus, the tolerability of nearly 500 medications varies by up to fivefold according to circadian scheduling, both in experimental models and/or patients. Moreover, treatment itself disrupted, maintained, or improved the circadian timing system as a function of drug timing. Improved patient outcomes on circadian-based treatments (chronotherapy) have been demonstrated in randomized clinical trials, especially for cancer and inflammatory diseases. However, recent technological advances have highlighted large interpatient differences in circadian functions resulting in significant variability in chronotherapy response. Such findings advocate for the advancement of personalized chronotherapeutics through interdisciplinary systems approaches. Thus, the combination of mathematical, statistical, technological, experimental, and clinical expertise is now shaping the development of dedicated devices and diagnostic and delivery algorithms enabling treatment individualization. In particular, multiscale systems chronopharmacology approaches currently combine mathematical modeling based on cellular and whole-body physiology to preclinical and clinical investigations toward the design of patient-tailored chronotherapies. We review recent systems research works aiming to the individualization of disease treatment, with emphasis on both cancer management and circadian timing system–resetting strategies for improving chronic disease control and patient outcomes. The American Society for Pharmacology and Experimental Therapeutics 2017-04 2017-04 /pmc/articles/PMC5394920/ /pubmed/28351863 http://dx.doi.org/10.1124/pr.116.013441 Text en Copyright © 2017 by The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the CC BY Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Articles
Ballesta, Annabelle
Innominato, Pasquale F.
Dallmann, Robert
Rand, David A.
Lévi, Francis A.
Systems Chronotherapeutics
title Systems Chronotherapeutics
title_full Systems Chronotherapeutics
title_fullStr Systems Chronotherapeutics
title_full_unstemmed Systems Chronotherapeutics
title_short Systems Chronotherapeutics
title_sort systems chronotherapeutics
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394920/
https://www.ncbi.nlm.nih.gov/pubmed/28351863
http://dx.doi.org/10.1124/pr.116.013441
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