| Literature DB >> 27575429 |
Susan L Makris1, Cheryl Siegel Scott2, John Fox2, Thomas B Knudsen3, Andrew K Hotchkiss4, Xabier Arzuaga2, Susan Y Euling2, Christina M Powers5, Jennifer Jinot2, Karen A Hogan2, Barbara D Abbott6, E Sidney Hunter6, Michael G Narotsky6.
Abstract
The 2011 EPA trichloroethylene (TCE) IRIS assessment, used developmental cardiac defects from a controversial drinking water study in rats (Johnson et al. [51]), along with several other studies/endpoints to derive reference values. An updated literature search of TCE-related developmental cardiac defects was conducted. Study quality, strengths, and limitations were assessed. A putative adverse outcome pathway (AOP) construct was developed to explore key events for the most commonly observed cardiac dysmorphologies, particularly those involved with epithelial-mesenchymal transition (EMT) of endothelial origin (EndMT); several candidate pathways were identified. A hypothesis-driven weight-of-evidence analysis of epidemiological, toxicological, in vitro, in ovo, and mechanistic/AOP data concluded that TCE has the potential to cause cardiac defects in humans when exposure occurs at sufficient doses during a sensitive window of fetal development. The study by Johnson et al. [51] was reaffirmed as suitable for hazard characterization and reference value derivation, though acknowledging study limitations and uncertainties. Published by Elsevier Inc.Entities:
Keywords: AOP; Cardiac; Malformations; TCE; Trichloroethylene
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Year: 2016 PMID: 27575429 PMCID: PMC9113522 DOI: 10.1016/j.reprotox.2016.08.014
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.421