4.5 Article

Per- and polyfluoroalkyl substances (PFAS) in mixtures show additive effects on transcriptomic points of departure in human liver spheroids

Journal

TOXICOLOGICAL SCIENCES
Volume 194, Issue 1, Pages 38-52

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/toxsci/kfad044

Keywords

TempO-Seq; PFAS; liver spheroids; benchmark concentration; new approach methodology; mixture toxicity

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Per- and polyfluoroalkyl substances (PFAS) are widely used chemicals that result in direct human exposure through various products. This study investigates the transcriptomic potency of PFAS mixtures using gene expression data from liver cell spheroids exposed to single PFAS and mixture exposures. The results suggest that the effects of PFAS mixtures on gene expression largely follow the predicted response through concentration addition, indicating absence of strong synergistic or antagonistic effects.
Per- and polyfluoroalkyl substances (PFAS) are a wide range of chemicals that are used in a variety of consumer and industrial products leading to direct human exposure. Many PFAS are chemically nonreactive and persistent in the environment, resulting in additional exposure from water, soil, and dietary intake. While some PFAS have documented negative health effects, data on simultaneous exposures to multiple PFAS (PFAS mixtures) are inadequate for making informed decisions for risk assessment. The current study leverages data from previous work in our group using Templated Oligo-Sequencing (TempO-Seq) for high-throughput transcriptomic analysis of PFAS-exposed primary human liver cell spheroids; herein, we determine the transcriptomic potency of PFAS in mixtures. Gene expression data from single PFAS and mixture exposures of liver cell spheroids were subject to benchmark concentration (BMC) analysis. We used the 25th lowest gene BMC as the point of departure to compare the potencies of single PFAS to PFAS mixtures of varying complexity and composition. Specifically, the empirical potency of 8 PFAS mixtures were compared to predicted mixture potencies calculated using the principal of concentration addition (ie, dose addition) in which mixture component potencies are summed by proportion to predict mixture potency. In this study, for most mixtures, empirical mixture potencies were comparable to potencies calculated through concentration addition. This work supports that the effects of PFAS mixtures on gene expression largely follow the concentration addition predicted response and suggests that effects of these individual PFAS in mixtures are not strongly synergistic or antagonistic.

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