Evidence map›Paper›PMID 36722664›Full record

ArticleEMBO molecular medicine2023

Targetable Brg1-CXCL14 axis contributes to alcoholic liver injury by driving neutrophil trafficking.

Nan Li, Hong Liu, Yujia Xue, Zheng Xu, Xiulian Miao, Yan Guo, Zilong Li, Zhiwen Fan, Yong Xu

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.2field-weighted citation impact, top 4% of its field
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

17 citing papers in PubMed, 34 citations in OpenAlex.

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  7. Epigenetics-targeted drugs: current paradigms and future challenges.Signal transduction and targeted therapy · 2024
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  10. The p21Toxicology · 2024
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  12. Platelets in Alcohol-Associated Liver Disease: Interaction With Neutrophils.Cellular and molecular gastroenterology and hepatology · 2024
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
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

9 authors at 4 institutions in 1 country.

Nan LiKey Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysiology, Nanjing Medical University, Nanjing, China.
Hong LiuKey Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysiology, Nanjing Medical University, Nanjing, China.
Yujia XueKey Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysiology, Nanjing Medical University, Nanjing, China.
Zheng XuKey Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysiology, Nanjing Medical University, Nanjing, China.
Xiulian MiaoCollage of Life Sciences and Institute of Biomedical Research, Liaocheng University, Liaocheng, China.
Yan GuoCollage of Life Sciences and Institute of Biomedical Research, Liaocheng University, Liaocheng, China.
Zilong LiState Key Laboratory of Natural Medicines, Department of Pharmacology, China Pharmaceutical University, Nanjing, China.ORCID 0000-0001-6839-0883
Zhiwen FanDepartment of Pathology, Nanjing Drum Tower Hospital Affiliated to Nanjing University Medical School, Nanjing, China.ORCID 0000-0001-7368-814X
Yong XuKey Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysiology, Nanjing Medical University, Nanjing, China.ORCID 0000-0003-1470-9371
Nanjing Medical University · CNChina Pharmaceutical University · CNLiaocheng University · CNNanjing Drum Tower Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alcoholic liver disease (ALD) accounts for a large fraction of patients with cirrhosis and hepatocellular carcinoma. In the present study we investigated the involvement of Brahma-related gene 1 (Brg1) in ALD pathogenesis and implication in ALD intervention. We report that Brg1 expression was elevated in mouse models of ALD, in hepatocyte exposed to alcohol, and in human ALD specimens. Manipulation of Brg1 expression in hepatocytes influenced the development of ALD in mice. Flow cytometry showed that Brg1 deficiency specifically attenuated hepatic infiltration of Ly6G

Indexed as

Chemokines, CXCLiver Diseases, AlcoholicNeutrophilsAnimalsDisease Models, AnimalDNA HelicasesHepatocytesHumansLiverMiceNuclear ProteinsTranscription FactorsChemokines, CXCCXCL14 protein, humanCXCL14 protein, mouseDNA HelicasesNuclear ProteinsSMARCA4 protein, humanSmarca4 protein, mouseTranscription Factorsalcoholic live diseasechemokinechromatin remodeling proteinneutrophil migrationtranscriptional regulation

Identifiers

PMID36722664
PMCPMC9994483
OpenAlexW4318754374

What Socratic 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 Socratic graph.