Evidence map›Paper›PMID 41871202›Full record

ArticleEnvironmental science & technology2026

Predifferentiation Neurotoxicity of GenX Exposure on hiPSC-Derived Cortical Neurons.

Shichen Wu, Junkai Xie, Xihui Zhao, Han Zhao, Oscar F Sánchez, Serena Yu, Jean-Christophe Rochet, Jennifer L Freeman, Chongli Yuan

Abstract read
In one paragraph

Article in Environmental science & technology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Shichen WuDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Junkai XieDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Xihui ZhaoDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Han ZhaoDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Oscar F SánchezDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Serena YuSchool of Health Sciences, Purdue University, West Lafayette, Indiana 47907, United States.
Jean-Christophe RochetBorch Department of Medicinal Chemistry and Molecular Pharmacy, Purdue University, West Lafayette, Indiana 47907, United States.ORCID 0000-0002-6484-1541
Jennifer L FreemanSchool of Health Sciences, Purdue University, West Lafayette, Indiana 47907, United States.ORCID 0000-0002-3669-9111
Chongli YuanDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.ORCID 0000-0003-3765-0931

Funding

Modeling functional genomics of susceptibility to the persistent effects of environmental toxins in an elderly rural Indiana neurodegenerative cohortR01AG080917 · NIA · PURDUE UNIVERSITY · PI Aaron B Bowman, Chongli Yuan · 2022 to 2026
$4.1M
Comparative neurotoxicity of PFASR01ES035429 · NIEHS · PURDUE UNIVERSITY · PI Jennifer L. Freeman, Chongli Yuan · 2024 to 2026
$2.0M
NIA NIH HHS R01 AG080917NIEHS NIH HHS R01 ES035429
6 · The paper itself

Abstract

Hexafluoropropylene oxide dimer acid (HFPO-DA), commercially known as GenX, was introduced as a potentially safer substitute for an older type of per- and polyfluorinated substance (PFAS) named perfluorooctanoic acid (PFOA). Emerging evidence suggests that GenX may possess neurotoxicity comparable to or greater than that of PFOA, underscoring the need for evaluating its potential to induce adverse health effects on the central nervous system. Here, we performed a systematic evaluation of predifferentiation GenX exposure and its neurotoxic effects utilizing human induced pluripotent stem cell (hiPSC)-derived cortical neurons. Neurons exposed to 0.4 and 4 ppb GenX prior to differentiation possess altered neuronal characteristics including synaptic density and neural activity, accompanied by transcriptomic changes associated with neurodegeneration, including enriched differentially expressed genes (DEGs) in the Alzheimer's disease (AD) pathway and predicted dysregulation of amyloid processing. Consistent with the transcriptomic alterations, GenX exposure altered multiple APP processing readouts, including increased sAPPβ/sAPPα ratios and intracellular C99 accumulation, accompanied by reduced extracellular Aβ40 and Aβ42 levels. Hyperphosphorylation of tau was also observed along with lipid droplet accumulation and reduced global translational activity, indicating broader disruptions. Collectively, our findings suggest that GenX exposure prior to differentiation, mimicking developmental exposure, can lead to persistent molecular and functional alterations in human cortical neurons that resemble key features observed in neurodegenerative diseases.

Indexed as

Induced Pluripotent Stem CellsNeuronsCell DifferentiationFluorocarbonsHumansFluorocarbonsAlzheimer’s diseaseGenX exposurehiPSC-derived cortical neuronsneurotoxicityPFAS

Identifiers

PMID41871202
PMCPMC13051483

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.