Evidence map›Paper›PMID 40133627›Full record

ArticleActa pharmacologica Sinica2025

Hepatocyte cellular repressor of E1A-stimulated genes 1 protects against acetaminophen-induced liver injury by promoting autophagy.

Qian-Ying Cheng, Miao-Miao Wu, Xiao-Li Wei, Li-Li Lu, Run-Dong Liu, Yuan-Hao Li, Ni-Na Zhu, Ya-Qun Li, Li Zuo, Hua Wang

Abstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Qian-Ying Cheng *Department of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Miao-Miao Wu *Department of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Xiao-Li Wei *Department of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Li-Li LuDepartment of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Run-Dong LiuDepartment of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Yuan-Hao LiInflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Medical University, Hefei, 230032, China.
Ni-Na ZhuSchool of Basic Medical Sciences, Molecular Biology Laboratory, Anhui Medical University, Hefei, 230032, China.
Ya-Qun LiSchool of Basic Medical Sciences, Molecular Biology Laboratory, Anhui Medical University, Hefei, 230032, China.
Li ZuoSchool of Basic Medical Sciences, Molecular Biology Laboratory, Anhui Medical University, Hefei, 230032, China. zuoli@ahmu.edu.cn.
Hua WangDepartment of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China. wanghua@ahmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acetaminophen-induced liver injury (AILI) accounts for a significant proportion of acute liver failure emphasizing the critical need to elucidate AILI pathogenesis and to identify effective therapeutic agents. Cellular repressor of E1A-stimulated genes 1 (CREG1) is a secreted glycoprotein that plays a crucial role in maintaining liver homeostasis. Prior studies have shown that CREG1 mitigates liver injury, steatosis, and inflammation associated with multiple liver diseases. In this study we investigated the role and therapeutic potential of CREG1 in AILI. We showed that the expression levels of CREG1 were markedly elevated in livers of AILI mice and patients with drug-induced liver injury (DILI), which was also observed in primary hepatocytes treated with acetaminophen (APAP). Hepatocyte-specific CREG1 deficiency mice were more sensitive to APAP compared to Creg1

Indexed as

AcetaminophenAutophagyChemical and Drug Induced Liver InjuryHepatocytesAMP-Activated Protein KinasesAnimalsGTPase-Activating ProteinsHumansMaleMiceMice, Inbred C57BLMice, KnockoutAcetaminophenAMP-Activated Protein KinasesGTPase-Activating ProteinsRalbp1 protein, mouseAILIAMP-dependent protein kinaseautophagyCREG1inflammation

Identifiers

PMID40133627
PMCPMC12274507

What OpenQuestion holds

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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.