Evidence map›Paper›PMID 28433418›Full record

ArticleAlcohol (Fayetteville, N.Y.)2017

Binge alcohol alters PNPLA3 levels in liver through epigenetic mechanism involving histone H3 acetylation.

Ricardo J Restrepo, Robert W Lim, Ronald J Korthuis, Shivendra D Shukla

Open access · greenAbstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. SIRT1 mediates nutritional regulation of SREBP-1c-driven hepatic PNPLA3 transcription via modulation of H3k9 acetylation.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2022
    Article
  5. Epigenetics of alcohol-related liver diseases.JHEP reports : innovation in hepatology · 2022
    Review
  6. Article
  7. Interaction Between Alcohol Consumption and PNPLA3 Variant in the Prevalence of Hepatic Steatosis in the US Population.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2021
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. 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

4 authors at 1 institution in 1 country.

Ricardo J RestrepoDepartment of Medical Pharmacology & Physiology, University of Missouri School of Medicine, Columbia, MO 65212, USA.
Robert W LimDepartment of Medical Pharmacology & Physiology, University of Missouri School of Medicine, Columbia, MO 65212, USA.
Ronald J KorthuisDepartment of Medical Pharmacology & Physiology, University of Missouri School of Medicine, Columbia, MO 65212, USA.
Shivendra D ShuklaDepartment of Medical Pharmacology & Physiology, University of Missouri School of Medicine, Columbia, MO 65212, USA. Electronic address: shuklaSD@missouri.edu.
University of Missouri · US

Funding

Daily Moderate Ethanol Ingestion Attenuates Postischemic Microvascular DysfunctioR01AA022108 · NIAAA · UNIVERSITY OF MISSOURI-COLUMBIA · PI KORTHUIS, RONALD JOHN · 2015 to 2019
$1.7M
NIAAA NIH HHS R01 AA022108
6 · The paper itself

Abstract

The human PNPLA3 (patatin-like phospholipase domain-containing 3) gene codes for a protein which is highly expressed in adipose tissue and liver, and is implicated in lipid homeostasis. While PNPLA3 protein contains regions homologous to functional lipolytic proteins, the regulation of its tissue expression is reflective of lipogenic genes. A naturally occurring genetic variant of PNPLA3 in humans has been linked to increased susceptibility to alcoholic liver disease. We have examined the modulatory effect of alcohol on PNPLA3 protein and mRNA expression as well as the association of its gene promoter with acetylated histone H3K9 by chromatin immunoprecipitation (ChIP) assay in rat hepatocytes in vitro, and in vivo in mouse and rat models of acute binge, chronic, and chronic followed by acute binge ethanol administration. Protein expression of PNPLA3 was significantly increased by alcohol in all three models used. PNPLA3 mRNA also increased, albeit to a varying degree. ChIP assay using H3AcK9 antibody showed increased association with the promoter of PNPLA3 in hepatocytes and in mouse liver. This was less evident in rat livers in vivo except under chronic treatment. It is concluded for the first time that histone acetylation plays a role in the modulation of PNPLA3 levels in the liver exposed to binge ethanol both in vitro and in vivo.

Indexed as

AcetylationAcyltransferasesAnimalsBinge DrinkingCells, CulturedDisease Models, AnimalEnzyme InductionEpigenesis, GeneticEthanolHistonesLiverMaleMembrane ProteinsMice, Inbred C57BLPhospholipases A2Phospholipases A2, Calcium-IndependentAcyltransferasesEthanolHistonesMembrane ProteinsPhospholipases A2Phospholipases A2, Calcium-IndependentPNPLA3 protein, mousePNPLA3 protein, ratRNA, MessengerBinge ethanolChronic-binge ethanolEpigeneticsHistone acetylationPNPLA3

Identifiers

PMID28433418
PMCPMC5533086
OpenAlexW2594612885

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.