John T. Gamble , Jesse Rogers , Kristen Breaux , Madison Feshuk , Carter Thunes , Katie Paul Friedman , Chad Deisenroth
{"title":"在DevTox胚层报告平台上筛选工业化学品对人类发育的毒性。","authors":"John T. Gamble , Jesse Rogers , Kristen Breaux , Madison Feshuk , Carter Thunes , Katie Paul Friedman , Chad Deisenroth","doi":"10.1016/j.tox.2025.154232","DOIUrl":null,"url":null,"abstract":"<div><div>The EPA New Chemicals Collaborative Research Program (NCCRP) seeks to maximize the efficiency and robustness of the new chemical review process under the Toxic Substances Control Act (TSCA) using new approach methods (NAMs) that represent the best available science. Consideration of the possible health hazards to pregnant women, and their developing offspring, for new chemical submissions is challenged by an insufficient number of acceptable screening modalities to quickly identify potential hazards to humans. The DevTox Germ Layer Reporter (GLR) assay platform evaluates chemical effects on early germ layer development and has been demonstrated to be a viable option for rapid chemical screening. The objective of this study was to screen a structurally diverse set of 171 representative chemicals selected from the TSCA non-confidential active inventory, and 54 <em>in vitro</em> assay reference chemicals, for potential developmental toxicity in the DevTox GLR-Endo assay. Assay performance metrics, as well as predictivity across a set of 16 reference developmental toxicants, were consistent with prior reporting and within acceptable parameters. Of the 38 reference chemicals not previously evaluated in the assay, 25 were identified as active, with 13 demonstrating selectivity for the SOX17 assay endpoint. For the test chemical set, 60 of the 165 chemicals analyzed were active, with 29 exhibiting a degree of selective activity. The results provide coverage of a critical toxicological domain for a set of chemicals relevant to the development of NAM-based methods for the NCCRP and may inform the development of tools in a NAMs-based hazard assessment strategy.</div></div>","PeriodicalId":23159,"journal":{"name":"Toxicology","volume":"517 ","pages":"Article 154232"},"PeriodicalIF":4.8000,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Screening industrial chemicals for human developmental toxicity in the DevTox Germ Layer Reporter platform\",\"authors\":\"John T. Gamble , Jesse Rogers , Kristen Breaux , Madison Feshuk , Carter Thunes , Katie Paul Friedman , Chad Deisenroth\",\"doi\":\"10.1016/j.tox.2025.154232\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The EPA New Chemicals Collaborative Research Program (NCCRP) seeks to maximize the efficiency and robustness of the new chemical review process under the Toxic Substances Control Act (TSCA) using new approach methods (NAMs) that represent the best available science. Consideration of the possible health hazards to pregnant women, and their developing offspring, for new chemical submissions is challenged by an insufficient number of acceptable screening modalities to quickly identify potential hazards to humans. The DevTox Germ Layer Reporter (GLR) assay platform evaluates chemical effects on early germ layer development and has been demonstrated to be a viable option for rapid chemical screening. The objective of this study was to screen a structurally diverse set of 171 representative chemicals selected from the TSCA non-confidential active inventory, and 54 <em>in vitro</em> assay reference chemicals, for potential developmental toxicity in the DevTox GLR-Endo assay. Assay performance metrics, as well as predictivity across a set of 16 reference developmental toxicants, were consistent with prior reporting and within acceptable parameters. Of the 38 reference chemicals not previously evaluated in the assay, 25 were identified as active, with 13 demonstrating selectivity for the SOX17 assay endpoint. For the test chemical set, 60 of the 165 chemicals analyzed were active, with 29 exhibiting a degree of selective activity. The results provide coverage of a critical toxicological domain for a set of chemicals relevant to the development of NAM-based methods for the NCCRP and may inform the development of tools in a NAMs-based hazard assessment strategy.</div></div>\",\"PeriodicalId\":23159,\"journal\":{\"name\":\"Toxicology\",\"volume\":\"517 \",\"pages\":\"Article 154232\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-07-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Toxicology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0300483X2500191X\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0300483X2500191X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Screening industrial chemicals for human developmental toxicity in the DevTox Germ Layer Reporter platform
The EPA New Chemicals Collaborative Research Program (NCCRP) seeks to maximize the efficiency and robustness of the new chemical review process under the Toxic Substances Control Act (TSCA) using new approach methods (NAMs) that represent the best available science. Consideration of the possible health hazards to pregnant women, and their developing offspring, for new chemical submissions is challenged by an insufficient number of acceptable screening modalities to quickly identify potential hazards to humans. The DevTox Germ Layer Reporter (GLR) assay platform evaluates chemical effects on early germ layer development and has been demonstrated to be a viable option for rapid chemical screening. The objective of this study was to screen a structurally diverse set of 171 representative chemicals selected from the TSCA non-confidential active inventory, and 54 in vitro assay reference chemicals, for potential developmental toxicity in the DevTox GLR-Endo assay. Assay performance metrics, as well as predictivity across a set of 16 reference developmental toxicants, were consistent with prior reporting and within acceptable parameters. Of the 38 reference chemicals not previously evaluated in the assay, 25 were identified as active, with 13 demonstrating selectivity for the SOX17 assay endpoint. For the test chemical set, 60 of the 165 chemicals analyzed were active, with 29 exhibiting a degree of selective activity. The results provide coverage of a critical toxicological domain for a set of chemicals relevant to the development of NAM-based methods for the NCCRP and may inform the development of tools in a NAMs-based hazard assessment strategy.
期刊介绍:
Toxicology is an international, peer-reviewed journal that publishes only the highest quality original scientific research and critical reviews describing hypothesis-based investigations into mechanisms of toxicity associated with exposures to xenobiotic chemicals, particularly as it relates to human health. In this respect "mechanisms" is defined on both the macro (e.g. physiological, biological, kinetic, species, sex, etc.) and molecular (genomic, transcriptomic, metabolic, etc.) scale. Emphasis is placed on findings that identify novel hazards and that can be extrapolated to exposures and mechanisms that are relevant to estimating human risk. Toxicology also publishes brief communications, personal commentaries and opinion articles, as well as concise expert reviews on contemporary topics. All research and review articles published in Toxicology are subject to rigorous peer review. Authors are asked to contact the Editor-in-Chief prior to submitting review articles or commentaries for consideration for publication in Toxicology.