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Population-Based in Vitro Hazard and Concentration–Response Assessment of Chemicals: The 1000 Genomes High-Throughput Screening Study

Background: Understanding of human variation in toxicity to environmental chemicals remains limited, so human health risk assessments still largely rely on a generic 10-fold factor (10(½) each for toxicokinetics and toxicodynamics) to account for sensitive individuals or subpopulations. Objectives:...

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Autores principales: Abdo, Nour, Xia, Menghang, Brown, Chad C., Kosyk, Oksana, Huang, Ruili, Sakamuru, Srilatha, Zhou, Yi-Hui, Jack, John R., Gallins, Paul, Xia, Kai, Li, Yun, Chiu, Weihsueh A., Motsinger-Reif, Alison A., Austin, Christopher P., Tice, Raymond R., Rusyn, Ivan, Wright, Fred A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: NLM-Export 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421772/
https://www.ncbi.nlm.nih.gov/pubmed/25622337
http://dx.doi.org/10.1289/ehp.1408775
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author Abdo, Nour
Xia, Menghang
Brown, Chad C.
Kosyk, Oksana
Huang, Ruili
Sakamuru, Srilatha
Zhou, Yi-Hui
Jack, John R.
Gallins, Paul
Xia, Kai
Li, Yun
Chiu, Weihsueh A.
Motsinger-Reif, Alison A.
Austin, Christopher P.
Tice, Raymond R.
Rusyn, Ivan
Wright, Fred A.
author_facet Abdo, Nour
Xia, Menghang
Brown, Chad C.
Kosyk, Oksana
Huang, Ruili
Sakamuru, Srilatha
Zhou, Yi-Hui
Jack, John R.
Gallins, Paul
Xia, Kai
Li, Yun
Chiu, Weihsueh A.
Motsinger-Reif, Alison A.
Austin, Christopher P.
Tice, Raymond R.
Rusyn, Ivan
Wright, Fred A.
author_sort Abdo, Nour
collection PubMed
description Background: Understanding of human variation in toxicity to environmental chemicals remains limited, so human health risk assessments still largely rely on a generic 10-fold factor (10(½) each for toxicokinetics and toxicodynamics) to account for sensitive individuals or subpopulations. Objectives: We tested a hypothesis that population-wide in vitro cytotoxicity screening can rapidly inform both the magnitude of and molecular causes for interindividual toxicodynamic variability. Methods: We used 1,086 lymphoblastoid cell lines from the 1000 Genomes Project, representing nine populations from five continents, to assess variation in cytotoxic response to 179 chemicals. Analysis included assessments of population variation and heritability, and genome-wide association mapping, with attention to phenotypic relevance to human exposures. Results: For about half the tested compounds, cytotoxic response in the 1% most “sensitive” individual occurred at concentrations within a factor of 10(½) (i.e., approximately 3) of that in the median individual; however, for some compounds, this factor was > 10. Genetic mapping suggested important roles for variation in membrane and transmembrane genes, with a number of chemicals showing association with SNP rs13120371 in the solute carrier SLC7A11, previously implicated in chemoresistance. Conclusions: This experimental approach fills critical gaps unaddressed by recent large-scale toxicity testing programs, providing quantitative, experimentally based estimates of human toxicodynamic variability, and also testable hypotheses about mechanisms contributing to interindividual variation. Citation: Abdo N, Xia M, Brown CC, Kosyk O, Huang R, Sakamuru S, Zhou YH, Jack JR, Gallins P, Xia K, Li Y, Chiu WA, Motsinger-Reif AA, Austin CP, Tice RR, Rusyn I, Wright FA. 2015. Population-based in vitro hazard and concentration–response assessment of chemicals: the 1000 Genomes high-throughput screening study. Environ Health Perspect 123:458–466; http://dx.doi.org/10.1289/ehp.1408775
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spelling pubmed-44217722015-05-07 Population-Based in Vitro Hazard and Concentration–Response Assessment of Chemicals: The 1000 Genomes High-Throughput Screening Study Abdo, Nour Xia, Menghang Brown, Chad C. Kosyk, Oksana Huang, Ruili Sakamuru, Srilatha Zhou, Yi-Hui Jack, John R. Gallins, Paul Xia, Kai Li, Yun Chiu, Weihsueh A. Motsinger-Reif, Alison A. Austin, Christopher P. Tice, Raymond R. Rusyn, Ivan Wright, Fred A. Environ Health Perspect Research Background: Understanding of human variation in toxicity to environmental chemicals remains limited, so human health risk assessments still largely rely on a generic 10-fold factor (10(½) each for toxicokinetics and toxicodynamics) to account for sensitive individuals or subpopulations. Objectives: We tested a hypothesis that population-wide in vitro cytotoxicity screening can rapidly inform both the magnitude of and molecular causes for interindividual toxicodynamic variability. Methods: We used 1,086 lymphoblastoid cell lines from the 1000 Genomes Project, representing nine populations from five continents, to assess variation in cytotoxic response to 179 chemicals. Analysis included assessments of population variation and heritability, and genome-wide association mapping, with attention to phenotypic relevance to human exposures. Results: For about half the tested compounds, cytotoxic response in the 1% most “sensitive” individual occurred at concentrations within a factor of 10(½) (i.e., approximately 3) of that in the median individual; however, for some compounds, this factor was > 10. Genetic mapping suggested important roles for variation in membrane and transmembrane genes, with a number of chemicals showing association with SNP rs13120371 in the solute carrier SLC7A11, previously implicated in chemoresistance. Conclusions: This experimental approach fills critical gaps unaddressed by recent large-scale toxicity testing programs, providing quantitative, experimentally based estimates of human toxicodynamic variability, and also testable hypotheses about mechanisms contributing to interindividual variation. Citation: Abdo N, Xia M, Brown CC, Kosyk O, Huang R, Sakamuru S, Zhou YH, Jack JR, Gallins P, Xia K, Li Y, Chiu WA, Motsinger-Reif AA, Austin CP, Tice RR, Rusyn I, Wright FA. 2015. Population-based in vitro hazard and concentration–response assessment of chemicals: the 1000 Genomes high-throughput screening study. Environ Health Perspect 123:458–466; http://dx.doi.org/10.1289/ehp.1408775 NLM-Export 2015-01-13 2015-05 /pmc/articles/PMC4421772/ /pubmed/25622337 http://dx.doi.org/10.1289/ehp.1408775 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, “Reproduced with permission from Environmental Health Perspectives”); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Abdo, Nour
Xia, Menghang
Brown, Chad C.
Kosyk, Oksana
Huang, Ruili
Sakamuru, Srilatha
Zhou, Yi-Hui
Jack, John R.
Gallins, Paul
Xia, Kai
Li, Yun
Chiu, Weihsueh A.
Motsinger-Reif, Alison A.
Austin, Christopher P.
Tice, Raymond R.
Rusyn, Ivan
Wright, Fred A.
Population-Based in Vitro Hazard and Concentration–Response Assessment of Chemicals: The 1000 Genomes High-Throughput Screening Study
title Population-Based in Vitro Hazard and Concentration–Response Assessment of Chemicals: The 1000 Genomes High-Throughput Screening Study
title_full Population-Based in Vitro Hazard and Concentration–Response Assessment of Chemicals: The 1000 Genomes High-Throughput Screening Study
title_fullStr Population-Based in Vitro Hazard and Concentration–Response Assessment of Chemicals: The 1000 Genomes High-Throughput Screening Study
title_full_unstemmed Population-Based in Vitro Hazard and Concentration–Response Assessment of Chemicals: The 1000 Genomes High-Throughput Screening Study
title_short Population-Based in Vitro Hazard and Concentration–Response Assessment of Chemicals: The 1000 Genomes High-Throughput Screening Study
title_sort population-based in vitro hazard and concentration–response assessment of chemicals: the 1000 genomes high-throughput screening study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421772/
https://www.ncbi.nlm.nih.gov/pubmed/25622337
http://dx.doi.org/10.1289/ehp.1408775
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