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A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives

Comparative assessment of potential human health impacts is a critical step in evaluating both chemical alternatives and existing products on the market. Most alternatives assessments are conducted on a chemical-by-chemical basis and it is seldom acknowledged that humans are exposed to complex produ...

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Autores principales: Grimm, Fabian A., Iwata, Yasuhiro, Sirenko, Oksana, Chappell, Grace A., Wright, Fred A., Reif, David M., Braisted, John, Gerhold, David L., Yeakley, Joanne M., Shepard, Peter, Seligmann, Bruce, Roy, Tim, Boogaard, Peter J., Ketelslegers, Hans B., Rohde, Arlean M., Rusyn, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179981/
https://www.ncbi.nlm.nih.gov/pubmed/28035192
http://dx.doi.org/10.1039/c6gc01147k
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author Grimm, Fabian A.
Iwata, Yasuhiro
Sirenko, Oksana
Chappell, Grace A.
Wright, Fred A.
Reif, David M.
Braisted, John
Gerhold, David L.
Yeakley, Joanne M.
Shepard, Peter
Seligmann, Bruce
Roy, Tim
Boogaard, Peter J.
Ketelslegers, Hans B.
Rohde, Arlean M.
Rusyn, Ivan
author_facet Grimm, Fabian A.
Iwata, Yasuhiro
Sirenko, Oksana
Chappell, Grace A.
Wright, Fred A.
Reif, David M.
Braisted, John
Gerhold, David L.
Yeakley, Joanne M.
Shepard, Peter
Seligmann, Bruce
Roy, Tim
Boogaard, Peter J.
Ketelslegers, Hans B.
Rohde, Arlean M.
Rusyn, Ivan
author_sort Grimm, Fabian A.
collection PubMed
description Comparative assessment of potential human health impacts is a critical step in evaluating both chemical alternatives and existing products on the market. Most alternatives assessments are conducted on a chemical-by-chemical basis and it is seldom acknowledged that humans are exposed to complex products, not individual substances. Indeed, substances of Unknown or Variable composition, Complex reaction products, and Biological materials (UVCBs) are ubiquitous in commerce yet they present a major challenge for registration and health assessments. Here, we present a comprehensive experimental and computational approach to categorize UVCBs according to global similarities in their bioactivity using a suite of in vitro models. We used petroleum substances, an important group of UVCBs which are grouped for regulatory approval and read-across primarily on physico-chemical properties and the manufacturing process, and only partially based on toxicity data, as a case study. We exposed induced pluripotent stem cell-derived cardiomyocytes and hepatocytes to DMSO-soluble extracts of 21 petroleum substances from five product groups. Concentration-response data from high-content imaging in cardiomyocytes and hepatocytes, as well as targeted high-throughput transcriptomic analysis of the hepatocytes, revealed distinct groups of petroleum substances. Data integration showed that bioactivity profiling affords clustering of petroleum substances in a manner similar to the manufacturing process-based categories. Moreover, we observed a high degree of correlation between bioactivity profiles and physico-chemical properties, as well as improved groupings when chemical and biological data were combined. Altogether, we demonstrate how novel in vitro screening approaches can be effectively utilized in combination with physico-chemical characteristics to group complex substances and enable read-across. This approach allows for rapid and scientifically-informed evaluation of health impacts of both existing substances and their chemical alternatives.
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spelling pubmed-51799812016-12-27 A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives Grimm, Fabian A. Iwata, Yasuhiro Sirenko, Oksana Chappell, Grace A. Wright, Fred A. Reif, David M. Braisted, John Gerhold, David L. Yeakley, Joanne M. Shepard, Peter Seligmann, Bruce Roy, Tim Boogaard, Peter J. Ketelslegers, Hans B. Rohde, Arlean M. Rusyn, Ivan Green Chem Chemistry Comparative assessment of potential human health impacts is a critical step in evaluating both chemical alternatives and existing products on the market. Most alternatives assessments are conducted on a chemical-by-chemical basis and it is seldom acknowledged that humans are exposed to complex products, not individual substances. Indeed, substances of Unknown or Variable composition, Complex reaction products, and Biological materials (UVCBs) are ubiquitous in commerce yet they present a major challenge for registration and health assessments. Here, we present a comprehensive experimental and computational approach to categorize UVCBs according to global similarities in their bioactivity using a suite of in vitro models. We used petroleum substances, an important group of UVCBs which are grouped for regulatory approval and read-across primarily on physico-chemical properties and the manufacturing process, and only partially based on toxicity data, as a case study. We exposed induced pluripotent stem cell-derived cardiomyocytes and hepatocytes to DMSO-soluble extracts of 21 petroleum substances from five product groups. Concentration-response data from high-content imaging in cardiomyocytes and hepatocytes, as well as targeted high-throughput transcriptomic analysis of the hepatocytes, revealed distinct groups of petroleum substances. Data integration showed that bioactivity profiling affords clustering of petroleum substances in a manner similar to the manufacturing process-based categories. Moreover, we observed a high degree of correlation between bioactivity profiles and physico-chemical properties, as well as improved groupings when chemical and biological data were combined. Altogether, we demonstrate how novel in vitro screening approaches can be effectively utilized in combination with physico-chemical characteristics to group complex substances and enable read-across. This approach allows for rapid and scientifically-informed evaluation of health impacts of both existing substances and their chemical alternatives. Royal Society of Chemistry 2016-08-21 2016-05-16 /pmc/articles/PMC5179981/ /pubmed/28035192 http://dx.doi.org/10.1039/c6gc01147k Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Grimm, Fabian A.
Iwata, Yasuhiro
Sirenko, Oksana
Chappell, Grace A.
Wright, Fred A.
Reif, David M.
Braisted, John
Gerhold, David L.
Yeakley, Joanne M.
Shepard, Peter
Seligmann, Bruce
Roy, Tim
Boogaard, Peter J.
Ketelslegers, Hans B.
Rohde, Arlean M.
Rusyn, Ivan
A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives
title A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives
title_full A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives
title_fullStr A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives
title_full_unstemmed A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives
title_short A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives
title_sort chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179981/
https://www.ncbi.nlm.nih.gov/pubmed/28035192
http://dx.doi.org/10.1039/c6gc01147k
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