Evidence map›Paper›PMID 33177163›Full record

ArticleGut2021

ATF4 activation promotes hepatic mitochondrial dysfunction by repressing NRF1-TFAM signalling in alcoholic steatohepatitis.

Liuyi Hao, Wei Zhong, Haibo Dong, Wei Guo, Xinguo Sun, Wenliang Zhang, Ruichao Yue, Tianjiao Li, Alexandra Griffiths, Ali Reza Ahmadi and 3 more

Open access · greenAbstract read
In one paragraph

Article in Gut, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 159 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 1 country.

Liuyi HaoCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA.ORCID 0000-0002-5044-7711
Wei ZhongCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA.
Haibo DongCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA.
Wei GuoCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA.
Xinguo SunCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA.
Wenliang ZhangCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA.
Ruichao YueCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA.
Tianjiao LiCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA.
Alexandra GriffithsDepartment of Kinesiology and Nutrition, UIC, Chicago, Illinois, USA.
Ali Reza AhmadiDepartment of Surgery, Johns Hopkins Medicine, Baltimore, Maryland, USA.
Zhaoli SunDepartment of Surgery, Johns Hopkins Medicine, Baltimore, Maryland, USA.
Zhenyuan SongDepartment of Kinesiology and Nutrition, UIC, Chicago, Illinois, USA.
Zhanxiang ZhouCenter for Translational Biomedical Research, UNCG, Kannapolis, North Carolina, USA z_zhou@uncg.edu.
Johns Hopkins University · USUniversity of Illinois Chicago · USUniversity of North Carolina at Greensboro · US

Funding

Clinical Resources for Alcoholic Hepatitis InvestigationsR24AA025017 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI ZHAOLI SUN · 2016 to 2026
$6.6M
Aldehydes in Alcohol-Induced Organ InjuryR01AA020212 · NIAAA · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI ZHANXIANG ZHOU · 2010 to 2026
$6.4M
Lipotoxicity in Alcoholic Liver DiseaseR01AA018844 · NIAAA · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI ZHANXIANG ZHOU · 2009 to 2026
$6.0M
NIAAA NIH HHS R01 AA018844NIAAA NIH HHS R01 AA020212NIAAA NIH HHS R24 AA025017
6 · The paper itself

Abstract

objectiveMitochondrial dysfunction plays a dominant role in the pathogenesis of alcoholic liver disease (ALD); however, the underlying mechanisms remain to be fully understood. We previously found that hepatic activating transcription factor 4 (ATF4) activation was associated with mitochondrial dysfunction in ALD. This study aimed to investigate the function and mechanism of ATF4 in alcohol-induced hepatic mitochondrial dysfunction.

designATF4 activation was detected in the livers of patients with severe alcoholic hepatitis (AH). The role of ATF4 and mitochondrial transcription factor A (TFAM) in alcohol-induced liver damage was determined in hepatocyte-specific

resultsHepatic PERK-eIF2α-ATF4 ER stress signalling was upregulated in patients with AH. Hepatocyte-specific ablation of

conclusionThis study demonstrates that hepatic ATF4 plays a pathological role in alcohol-induced mitochondrial dysfunction and liver injury by disrupting the NRF1-TFAM pathway.

Indexed as

Up-RegulationActivating Transcription Factor 4AnimalsDNA-Binding ProteinseIF-2 KinaseFatty Liver, AlcoholicHumansMiceMice, KnockoutMitochondria, LiverMitochondrial ProteinsSignal TransductionTranscription FactorsActivating Transcription Factor 4DNA-Binding ProteinsEIF2AK3 protein, humaneIF-2 KinaseELF2 protein, humanMitochondrial Proteinsmitochondrial transcription factor ATranscription Factorsalcoholic liver diseaseenergy metabolismhepatocyte

Identifiers

PMID33177163
PMCPMC8110597
OpenAlexW3098787407

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.