Evidence map›Paper›PMID 42353825›Full record

ArticleGenes2026

Integrative Network Toxicology Reveals Potential Molecular Targets Linking Plasticizer Exposure to Inflammatory Gastrointestinal Disorders.

Yongqi Chen, Jiyuan Shi, Yun Ruan, Jinghan Guan, Miaohan Yan, Zongying Zhang, Luojin Wu, Mengmeng Sang, Xinfeng Wang, Liming Mao and 1 more

Abstract read
In one paragraph

Article in Genes, 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

11 authors.

Yongqi ChenDepartment of Gastroenterology and Hepatology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong 226001, China.
Jiyuan ShiDepartment of Immunology, School of Medicine, Nantong University, Nantong 226001, China.
Yun RuanDepartment of Gastroenterology and Hepatology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong 226001, China.
Jinghan GuanDepartment of Immunology, School of Medicine, Nantong University, Nantong 226001, China.
Miaohan YanDepartment of Immunology, School of Medicine, Nantong University, Nantong 226001, China.
Zongying ZhangDepartment of Gastroenterology and Hepatology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong 226001, China.
Luojin WuDepartment of Gastroenterology and Hepatology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong 226001, China.
Mengmeng SangDepartment of Immunology, School of Medicine, Nantong University, Nantong 226001, China.ORCID 0000-0001-5249-002X
Xinfeng WangDepartment of Hematology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong 226019, China.
Liming MaoDepartment of Immunology, School of Medicine, Nantong University, Nantong 226001, China.ORCID 0000-0002-9740-820X
Zhaoxiu LiuDepartment of Gastroenterology and Hepatology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong 226001, China.

Funding

National Natural Science Foundation of China 32270919
6 · The paper itself

Abstract

backgroundPlasticizers, including phthalate esters and phthalate-free alternatives, are widely detected environmental chemicals. Although increasing evidence suggests that plasticizers may disrupt gastrointestinal homeostasis, their potential molecular links with inflammatory gastrointestinal disorders (IGDs) remain unclear.

methodsThis study aimed to systematically identify potential molecular targets and pathways linking representative plasticizers with IGDs. An integrative network toxicology framework was applied to investigate four plasticizers, including dimethyl phthalate (DMP), diethyl phthalate (DEP), dioctyl phthalate/di(2-ethylhexyl) phthalate (DOP/DEHP), and acetyl tributyl citrate (ATBC), in relation to Crohn's disease (CD), ulcerative colitis (UC), esophagitis, and gastritis. Plasticizer- and disease-related targets were collected from public databases, followed by overlapping target screening, protein-protein interaction network analysis, functional enrichment analysis, GEO-based transcriptomic validation, molecular docking, molecular dynamics simulation, and single-cell RNA-seq analysis.

resultsDisease-specific candidate targets were identified, including

conclusionsThis study provides an exploratory network toxicology framework for identifying potential molecular associations between plasticizer exposure and IGDs. The findings highlight disease-specific and plasticizer-associated candidate targets that may guide future experimental validation and environmental risk assessment.

Indexed as

Gastrointestinal DiseasesPlasticizersHumansMolecular Docking SimulationProtein Interaction MapsPlasticizersATBCDEPDMPDOPinflammatory gastrointestinal disordersmolecular dockingnetwork toxicology

Identifiers

PMID42353825
PMCPMC13299468

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.