Estrogenic Activity of Structurally Distinct PFASs Through Estrogen Receptor Pathway

Perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), and perfluorohexane sulfonic acid (PFHxS) have been listed under the Stockholm Convention and are being progressively phased out worldwide; environmental prevalence and human exposure to other poly- and perfluoroalkyl substances (PFASs) with different structures are on the rise. However, the toxic effects and mechanisms of other PFASs remain unclear. This study explored and compared the estrogenic effects and underlying mechanisms of eight typical PFASs. PFOA, PFOS, PFHxS, and perfluorooctane sulfonamide (PFOSA) promoted the proliferation of MCF-7 cells, with PFOSA exhibiting the strongest estrogenic effect among the eight targeted PFASs. Specifically, for the PFASs with the same number of carbons and different functional groups, the estrogenic effect is in the decreasing order of PFOSA (sulfonamide group) > PFOS (sulfonic acid group) > PFOA (carboxylic acid group). The observed enhancement was likely caused by estrogen receptor (ER) activation, as an ER antagonist significantly inhibited the pro-proliferation effect. Luciferase reporter gene assays, fluorescence competitive binding assays, and molecular docking simulation were used to furnish supplementary evidence for the direct action of PFASs on the ER. PFOA, PFHxS, PFOS, and PFOSA can activate ER transcriptional activity and bind to the ER, demonstrating that ER is a potential target of PFASs. For PFOA, PFOS, and PFOSA, the rank order of binding affinities with ER in fluorescence competitive binding assays and the calculated binding energy in molecular docking simulation were consistent with the results of the cell proliferation experiment and luciferase reporter gene assays, suggesting that receptor binding affinity also plays a critical role in the activation effect of the ER pathway. Overall, our results indicate the estrogenic effects of other PFASs through ER-mediated pathways and elucidate the molecular mechanism for the different activity of eight PFASs, as well as suggest that PFOS precursors require more attention when determining the environmental risk of PFASs.

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Publication Details

Journal
Journal of Applied Toxicology
Published
2025-12-01
DOI
https://doi.org/10.1002/jat.70000
Citations
1
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
0.86

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article

Estrogenic Activity of Structurally Distinct PFASs Through Estrogen Receptor Pathway

Liang‐Hong Guo, Tingyu Lu, Kang Xie, Fangfang Li et al.
1 citations
Journal of Applied Toxicology
Per- and polyfluoroalkyl substances research
0.86
article

Estrogenic Activity of Structurally Distinct PFASs Through Estrogen Receptor Pathway

Liang‐Hong Guo, Tingyu Lu, Kang Xie, Fangfang Li, Yafang Chen, Minjie Li, Weichao Wu, Xinyi Zhou, Fanglin Hu
article en
1 citations

Abstract

Perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), and perfluorohexane sulfonic acid (PFHxS) have been listed under the Stockholm Convention and are being progressively phased out worldwide; environmental prevalence and human exposure to other poly- and perfluoroalkyl substances (PFASs) with different structures are on the rise. However, the toxic effects and mechanisms of other PFASs remain unclear. This study explored and compared the estrogenic effects and underlying mechanisms of eight typical PFASs. PFOA, PFOS, PFHxS, and perfluorooctane sulfonamide (PFOSA) promoted the proliferation of MCF-7 cells, with PFOSA exhibiting the strongest estrogenic effect among the eight targeted PFASs. Specifically, for the PFASs with the same number of carbons and different functional groups, the estrogenic effect is in the decreasing order of PFOSA (sulfonamide group) > PFOS (sulfonic acid group) > PFOA (carboxylic acid group). The observed enhancement was likely caused by estrogen receptor (ER) activation, as an ER antagonist significantly inhibited the pro-proliferation effect. Luciferase reporter gene assays, fluorescence competitive binding assays, and molecular docking simulation were used to furnish supplementary evidence for the direct action of PFASs on the ER. PFOA, PFHxS, PFOS, and PFOSA can activate ER transcriptional activity and bind to the ER, demonstrating that ER is a potential target of PFASs. For PFOA, PFOS, and PFOSA, the rank order of binding affinities with ER in fluorescence competitive binding assays and the calculated binding energy in molecular docking simulation were consistent with the results of the cell proliferation experiment and luciferase reporter gene assays, suggesting that receptor binding affinity also plays a critical role in the activation effect of the ER pathway. Overall, our results indicate the estrogenic effects of other PFASs through ER-mediated pathways and elucidate the molecular mechanism for the different activity of eight PFASs, as well as suggest that PFOS precursors require more attention when determining the environmental risk of PFASs.

Journal of Applied Toxicology
Zhejiang Academy of Social Sciences (CN), Hangzhou Academy of Agricultural Sciences (CN), ZheJiang Academy of Agricultural Sciences (CN), China Jiliang University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China, Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 21%
Per- and polyfluoroalkyl substances research
0.86
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