Evidence map›Paper›PMID 39472514›Full record

ArticleEMBO molecular medicine2024

Luteolin detoxifies DEHP and prevents liver injury by degrading Uroc1 protein in mice.

Huiting Wang, Ziting Zhao, Mingming Song, Wenxiang Zhang, Chang Liu, Siyu Chen

Abstract read
In one paragraph

Article in EMBO molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Drought Stress Mediated Changes in Food Crops: Mechanisms and Remediation Strategies.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

6 authors.

Huiting WangState Key Laboratory of Natural Medicines and School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211198, China.
Ziting ZhaoState Key Laboratory of Natural Medicines and School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211198, China.
Mingming SongState Key Laboratory of Natural Medicines and School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211198, China.
Wenxiang ZhangState Key Laboratory of Natural Medicines and School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211198, China. wenxiangzhang@cpu.edu.cn.ORCID http://orcid.org/0000-0002-1077-8014
Chang LiuState Key Laboratory of Natural Medicines and School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211198, China. changliu@cpu.edu.cn.ORCID http://orcid.org/0000-0001-9251-708X
Siyu ChenState Key Laboratory of Natural Medicines and School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211198, China. siyuchen@cpu.edu.cn.ORCID http://orcid.org/0000-0002-3809-1062

Funding

JST | Natural Science Foundation of Jiangsu Province (Jiangsu Natural Science Foundation) no. BK20220151MOST | National Key Research and Development Program of China (NKPs) no. 2021YFF0702000MOST | National Key Research and Development Program of China (NKPs) no. 2022YFA0807200MOST | National Natural Science Foundation of China (NSFC) no. 32471201MOST | National Natural Science Foundation of China (NSFC) no. 82470930| Natural Science Foundation of Xinjiang Uygur Autonomous Region (Xinjiang Natural Science Foundation) no. 2023D01D05| Natural Science Foundation of Xinjiang Uygur Autonomous Region (Xinjiang Natural Science Foundation) no. 2023D01D09the Natural Science Foundation of Chongqing, China CSTB2023NSCQ-MSX0094the Priority Academic Program Development of Jiangsu Higher Education Institutions PAPD
6 · The paper itself

Abstract

Di-(2-ethylhexyl) phthalate (DEHP), an environmental pollutant, has been widely detected in both environmental and clinical samples, representing a serious threat to the homeostasis of the endocrine system. The accumulation of DEHP is notably pronounced in the liver and can lead to liver damage. The lack of effective high-throughput screening system retards the discovery of such drugs that can specifically target and eliminate the detrimental impact of DEHP. Here, by developing a Cy5-modified single-strand DNA-aptamer-based approach targeting DEHP, we have identified luteolin as a potential drug, which showcasing robust efficacy in detoxifying the DEHP by facilitating the expulsion of DEHP in both mouse primary hepatocytes and livers. Mechanistically, luteolin enhances the protein degradation of hepatic urocanate hydratase 1 (Uroc1) by targeting its Ala270 and Val272 sites. More importantly, trans-urocanic acid (trans-UCA), as the substrate of Uroc1, possesses properties similar to luteolin by regulating the lysosomal exocytosis through the inhibition of the ERK1/2 signal cascade. In summary, luteolin serves as a potent therapeutic agent in efficiently detoxifying DEHP in the liver by regulating the UCA/Uroc1 axis.

Indexed as

Diethylhexyl PhthalateLuteolinAnimalsChemical and Drug Induced Liver InjuryHepatocytesHumansLiverMaleMiceMice, Inbred C57BLDiethylhexyl PhthalateLuteolinLiver InjuryLuteolinUroc1Visual DEHP Tracing System

Identifiers

PMID39472514
PMCPMC11555401

What OpenQuestion holds

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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.