Evidence map›Paper›PMID 24833709›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2014

The inhibitory effect of ethanol on Sestrin3 in the pathogenesis of ethanol-induced liver injury.

Xinqin Kang, Kateryna Petyaykina, Rongya Tao, Xiwen Xiong, X Charlie Dong, Suthat Liangpunsakul

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  11. Effect of ethanol on lipid metabolism.Journal of hepatology · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. The potential of sestrins as therapeutic targets for diabetes.Expert opinion on therapeutic targets · 2015
    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

6 authors at 2 institutions in 1 country.

Xinqin KangDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana;
Kateryna PetyaykinaDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana;
Rongya TaoDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana; and.
Xiwen XiongDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana; and.
X Charlie DongDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana; and.
Suthat LiangpunsakulDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; Roudebush Veterans Administration Medical Center, Indianapolis, Indiana sliangpu@iupui.edu.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Regulation of hepatic lipid metabolism by a novel Foxo pathwayR01DK091592 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI DONG, X. CHARLIE · 2012 to 2016
$1.7M
Effect of ethanol on Kupffer cell/hepatocyte interactions and lipid metabolismK08AA016570 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI LIANGPUNSAKUL, SUTHAT · 2008 to 2012
$659k
NIAAA NIH HHS K08 AA016570NIDDK NIH HHS R01 DK091592NIDDK NIH HHS R01-DK-091592
6 · The paper itself

Abstract

Sestrins (Sesns) are a family of stress-sensitive genes that have been suggested to regulate lipid metabolism. Chronic ethanol feeding is known to cause lipid accumulation in hepatocytes. This study was designed to investigate the role of Sesn3 in the pathogenesis of alcohol-induced hepatic steatosis. We demonstrated that ethanol inhibited the expression of Sesn3 in VL-17A cells. Overexpression of Sesn3 ameliorated triglyceride accumulation; downregulation using short hairpin RNA significantly deteriorated triglyceride accumulation in these cells. The expression of Sesn3 was also reduced in mice fed with ethanol for 4 wk. Overexpression of Sesn3 prevented hepatic steatosis, whereas knockdown of Sesn3 worsened hepatic steatosis in ethanol-fed mice. Overexpression of Sesn3 significantly reduced the expression of genes encoding for lipid synthesis through AMPK pathway. Overexpression of Sesn3 augmented the effect of ethanol on phospho-p70 S6 kinase. The levels of hepatic light chain 3, a marker for autophagy, expression were significantly decreased in ethanol-fed mice after Sesn3 gene was knocked down. Our findings suggest that inhibitory effect of ethanol on Sesn3 may play an important role in the development of ethanol-induced fatty liver.

Indexed as

EthanolAMP-Activated Protein KinasesAnimalsDisease Models, AnimalDown-RegulationFatty Liver, AlcoholicHeat-Shock ProteinsHep G2 CellsHumansLipogenesisLiverMaleMiceMice, Inbred C57BLMicrotubule-Associated ProteinsRibosomal Protein S6 Kinases, 70-kDaAMP-Activated Protein KinasesEthanolHeat-Shock ProteinsMap1lc3b protein, mouseMicrotubule-Associated ProteinsRibosomal Protein S6 Kinases, 70-kDaSESN3 protein, humanSesn3 protein, mouseSestrinsTriglyceridesalcoholSestrin3steatosis

Identifiers

PMID24833709
PMCPMC4080163
OpenAlexW2064209034

What OpenQuestion holds

Textmetadata
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.