Evidence map›Paper›PMID 41528243›Full record

ArticleEnvironmental science & technology2026

Hierarchical Mechanistic Modeling of Complex Toxicity Endpoints from Public Concentration-Response Data.

Elena Chung, Daniel P Russo, Lauren M Aleksunes, Genoa R Warner, Hao Zhu

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 authors.

Elena ChungDepartment of Chemistry and Biochemistry, Rowan University, Glassboro, New Jersey 08028, United States.ORCID 0000-0001-7577-9328
Daniel P RussoCenter for Biomedical Informatics and Genomics, School of Medicine, Tulane University, New Orleans, Louisiana 70112, United States.
Lauren M AleksunesDepartment of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, New Jersey 08854, United States.
Genoa R WarnerDepartment of Chemistry and Environmental Science, College of Science and Liberal Arts, New Jersey Institute of Technology, Newark, New Jersey 07103, United States.
Hao ZhuDepartment of Chemistry and Biochemistry, Rowan University, Glassboro, New Jersey 08028, United States.ORCID 0000-0002-3559-6129

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI BRIAN T BUCKLEY · 1988 to 2026
$47.4M
NJ ACTS: A Platform for Translational Science in New JerseyUM1TR004789 · NCATS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Reynold Alexander Panettieri · 2024 to 2026
$16.8M
Discovering Chemical Activity Networks-Predicting Bioactivity Based on StructureR35ES031709 · NIEHS · OREGON STATE UNIVERSITY · PI Robyn L Tanguay · 2021 to 2026
$5.2M
Integrated Transporter Elucidation CenterUC2HD113039 · NICHD · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Lauren M Aleksunes, Dongeun Huh · 2023 to 2026
$4.5M
Placental Responses to Environmental Chemicals - Diversity Supplement 2R01ES029275 · NIEHS · RUTGERS, THE STATE UNIV OF N.J. · PI ALEKSUNES, LAUREN M, BARRETT, EMILY S · 2018 to 2022
$3.2M
Mechanism-Driven Virtual Adverse Outcome Pathway Modeling for HepatotoxicityR01ES031080 · NIEHS · TULANE UNIVERSITY OF LOUISIANA · PI ZHU, HAO · 2020 to 2024
$2.3M
Mechanisms of Phthalate Toxicity in the OvaryR00ES031150 · NIEHS · NEW JERSEY INSTITUTE OF TECHNOLOGY · PI WARNER, GENOA R · 2022 to 2024
$1.1M
NCATS NIH HHS UM1 TR004789NICHD NIH HHS UC2 HD113039NIEHS NIH HHS P30 ES005022NIEHS NIH HHS R00 ES031150NIEHS NIH HHS R01 ES029275NIEHS NIH HHS R01 ES031080NIEHS NIH HHS R35 ES031709
6 · The paper itself

Abstract

High-throughput screening (HTS) programs have generated abundant data on numerous chemicals, supporting the discovery of toxicity mechanisms and advancing understanding of adverse outcome pathways (AOPs) in chemical toxicity. However, organizing and interpreting these data for predictive modeling remain challenging due to inconsistent repository formats, varied program objectives, heterogeneous assay targets, and differences in experimental protocols, including concentration ranges. To address these limitations, we developed a hierarchical mechanistic modeling framework that systematically structures and interprets concentration response HTS data. The model integrated curated data sets by mapping metadata from 455 PubChem assays to 216 protein targets and 103 biological pathways in WikiPathways. Assay-level concentration-response data were organized within a biologically layered hierarchy to construct AOP-based models. The resulting models generated pathway-level toxicity scores that quantified compound potency by integrating inferred protein activity and downstream pathway perturbations. In total, 103 pathways were statistically associated with five

Indexed as

Models, ChemicalToxicity TestsAnimalsHigh-Throughput Screening AssaysHumansadverse outcome pathwaysartificial intelligencebig datahierarchical modelinghigh-throughput screeningnew approach methodologiestoxicity prediction

Identifiers

PMID41528243
PMCPMC12854766

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.