Evidence map›Paper›PMID 42361056›Full record

ArticlePloS one2026

Toxicity analysis of food contaminants based on network toxicology and molecular docking: A case study of Zearalenone.

Xiaobo Xu, RuiLi Miao, Ping Xu, Leishan Chen, Kun Zhao, PingHui Xu, Hanna Fotina

Abstract read
In one paragraph

Article in PloS one, 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
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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

7 authors.

Xiaobo XuSchool of Biological Engineering, Xinxiang University, Xinxiang, China.
RuiLi MiaoSchool of Biological Engineering, Xinxiang University, Xinxiang, China.
Ping XuSchool of Biological Engineering, Xinxiang University, Xinxiang, China.ORCID https://orcid.org/0000-0002-3862-3567
Leishan ChenSchool of Biological Engineering, Xinxiang University, Xinxiang, China.
Kun ZhaoCollege of Animal Science and Veterinary Medicine, Henan Institute of Science and Technology, Xinxiang, China.
PingHui XuXinxiang Bokai Biotechnology Co., Ltd, Xinxiang, China.
Hanna FotinaLaboratory of Molecular Biology of Ticks, Department of Disease Vectors, Institute of Parasitology, Biology Centre CAS, Branisovska, Ceske Budejovice, Czech Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zearalenone (ZEA) is a non - steroid estrogen contaminant produced by fungi of the genus Fusarium. It is widely present in grains and seriously threatens global food safety. This study takes ZEA as an example to effectively evaluate the toxicity of food contaminants through network toxicology, molecular docking and molecular dynamics simulation strategies, and analyzes the molecular mechanism of its hypothesized toxicity - nephrotoxicity. The study found that ZEA affects immunotoxicity, inflammatory response, apoptosis, and cytogenetic mutations by regulating core targets such as STAT3, ESR1, HSP90AA1, MMP9, and MTOR, and regulating pathways such as the cancer pathway and the PI3K - Akt signaling pathway, ultimately leading to nephrotoxicity. The results of molecular docking and molecular dynamics simulation also showed good binding affinity between ZEA and core targets. This result provided a theoretical basis for understanding the molecular mechanism of ZEA - nephrotoxicity and for preventing and treating cancers caused by the food contaminant ZEA. In addition, the methods of network toxicology and molecular docking also provided an effective way to rapidly evaluate the toxicity of food contaminants, effectively addressing the cost and ethical issues associated with the use of experimental animals.

Indexed as

Food ContaminationMolecular Docking SimulationZearalenoneAnimalsApoptosisHumansMolecular Dynamics SimulationSignal TransductionZearalenone

Identifiers

PMID42361056
PMCPMC13308858

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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.