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Modeling Drug- and Chemical-Induced Hepatotoxicity with Systems Biology Approaches

We provide an overview of computational systems biology approaches as applied to the study of chemical- and drug-induced toxicity. The concept of “toxicity pathways” is described in the context of the 2007 US National Academies of Science report, “Toxicity testing in the 21st Century: A Vision and A...

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Autores principales: Bhattacharya, Sudin, Shoda, Lisl K.M., Zhang, Qiang, Woods, Courtney G., Howell, Brett A., Siler, Scott Q., Woodhead, Jeffrey L., Yang, Yuching, McMullen, Patrick, Watkins, Paul B., Andersen, Melvin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522076/
https://www.ncbi.nlm.nih.gov/pubmed/23248599
http://dx.doi.org/10.3389/fphys.2012.00462
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author Bhattacharya, Sudin
Shoda, Lisl K.M.
Zhang, Qiang
Woods, Courtney G.
Howell, Brett A.
Siler, Scott Q.
Woodhead, Jeffrey L.
Yang, Yuching
McMullen, Patrick
Watkins, Paul B.
Andersen, Melvin E.
author_facet Bhattacharya, Sudin
Shoda, Lisl K.M.
Zhang, Qiang
Woods, Courtney G.
Howell, Brett A.
Siler, Scott Q.
Woodhead, Jeffrey L.
Yang, Yuching
McMullen, Patrick
Watkins, Paul B.
Andersen, Melvin E.
author_sort Bhattacharya, Sudin
collection PubMed
description We provide an overview of computational systems biology approaches as applied to the study of chemical- and drug-induced toxicity. The concept of “toxicity pathways” is described in the context of the 2007 US National Academies of Science report, “Toxicity testing in the 21st Century: A Vision and A Strategy.” Pathway mapping and modeling based on network biology concepts are a key component of the vision laid out in this report for a more biologically based analysis of dose-response behavior and the safety of chemicals and drugs. We focus on toxicity of the liver (hepatotoxicity) – a complex phenotypic response with contributions from a number of different cell types and biological processes. We describe three case studies of complementary multi-scale computational modeling approaches to understand perturbation of toxicity pathways in the human liver as a result of exposure to environmental contaminants and specific drugs. One approach involves development of a spatial, multicellular “virtual tissue” model of the liver lobule that combines molecular circuits in individual hepatocytes with cell–cell interactions and blood-mediated transport of toxicants through hepatic sinusoids, to enable quantitative, mechanistic prediction of hepatic dose-response for activation of the aryl hydrocarbon receptor toxicity pathway. Simultaneously, methods are being developing to extract quantitative maps of intracellular signaling and transcriptional regulatory networks perturbed by environmental contaminants, using a combination of gene expression and genome-wide protein-DNA interaction data. A predictive physiological model (DILIsym™) to understand drug-induced liver injury (DILI), the most common adverse event leading to termination of clinical development programs and regulatory actions on drugs, is also described. The model initially focuses on reactive metabolite-induced DILI in response to administration of acetaminophen, and spans multiple biological scales.
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spelling pubmed-35220762012-12-17 Modeling Drug- and Chemical-Induced Hepatotoxicity with Systems Biology Approaches Bhattacharya, Sudin Shoda, Lisl K.M. Zhang, Qiang Woods, Courtney G. Howell, Brett A. Siler, Scott Q. Woodhead, Jeffrey L. Yang, Yuching McMullen, Patrick Watkins, Paul B. Andersen, Melvin E. Front Physiol Physiology We provide an overview of computational systems biology approaches as applied to the study of chemical- and drug-induced toxicity. The concept of “toxicity pathways” is described in the context of the 2007 US National Academies of Science report, “Toxicity testing in the 21st Century: A Vision and A Strategy.” Pathway mapping and modeling based on network biology concepts are a key component of the vision laid out in this report for a more biologically based analysis of dose-response behavior and the safety of chemicals and drugs. We focus on toxicity of the liver (hepatotoxicity) – a complex phenotypic response with contributions from a number of different cell types and biological processes. We describe three case studies of complementary multi-scale computational modeling approaches to understand perturbation of toxicity pathways in the human liver as a result of exposure to environmental contaminants and specific drugs. One approach involves development of a spatial, multicellular “virtual tissue” model of the liver lobule that combines molecular circuits in individual hepatocytes with cell–cell interactions and blood-mediated transport of toxicants through hepatic sinusoids, to enable quantitative, mechanistic prediction of hepatic dose-response for activation of the aryl hydrocarbon receptor toxicity pathway. Simultaneously, methods are being developing to extract quantitative maps of intracellular signaling and transcriptional regulatory networks perturbed by environmental contaminants, using a combination of gene expression and genome-wide protein-DNA interaction data. A predictive physiological model (DILIsym™) to understand drug-induced liver injury (DILI), the most common adverse event leading to termination of clinical development programs and regulatory actions on drugs, is also described. The model initially focuses on reactive metabolite-induced DILI in response to administration of acetaminophen, and spans multiple biological scales. Frontiers Media S.A. 2012-12-14 /pmc/articles/PMC3522076/ /pubmed/23248599 http://dx.doi.org/10.3389/fphys.2012.00462 Text en Copyright © 2012 Bhattacharya, Shoda, Zhang, Woods, Howell, Siler, Woodhead, Yang, McMullen, Watkins and Andersen. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Physiology
Bhattacharya, Sudin
Shoda, Lisl K.M.
Zhang, Qiang
Woods, Courtney G.
Howell, Brett A.
Siler, Scott Q.
Woodhead, Jeffrey L.
Yang, Yuching
McMullen, Patrick
Watkins, Paul B.
Andersen, Melvin E.
Modeling Drug- and Chemical-Induced Hepatotoxicity with Systems Biology Approaches
title Modeling Drug- and Chemical-Induced Hepatotoxicity with Systems Biology Approaches
title_full Modeling Drug- and Chemical-Induced Hepatotoxicity with Systems Biology Approaches
title_fullStr Modeling Drug- and Chemical-Induced Hepatotoxicity with Systems Biology Approaches
title_full_unstemmed Modeling Drug- and Chemical-Induced Hepatotoxicity with Systems Biology Approaches
title_short Modeling Drug- and Chemical-Induced Hepatotoxicity with Systems Biology Approaches
title_sort modeling drug- and chemical-induced hepatotoxicity with systems biology approaches
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522076/
https://www.ncbi.nlm.nih.gov/pubmed/23248599
http://dx.doi.org/10.3389/fphys.2012.00462
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