Evidence map›Paper›PMID 30030934›Full record

ArticleAlcoholism, clinical and experimental research2018

In Vivo Metabolic Tracing Demonstrates the Site-Specific Contribution of Hepatic Ethanol Metabolism to Histone Acetylation.

Crystina L Kriss, Emily Gregory-Lott, Aaron J Storey, Alan J Tackett, Wayne P Wahls, Stanley M Stevens

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Role of cellular senescence in hepatic diseases (Review).International journal of molecular medicine · 2025
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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.

Crystina L KrissDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, Florida.
Emily Gregory-LottDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, Florida.
Aaron J StoreyDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Alan J TackettDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Wayne P WahlsDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Stanley M StevensDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, Florida.ORCID 0000-0002-1399-0256
University of Arkansas for Medical Sciences · USUniversity of South Florida · US

Funding

Understanding Hesitant AdoptersP20GM103429 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI Lawrence E Cornett, JERRY WARE · 2012 to 2026
$60.9M
Translational Regulation in Normal Erythropoiesis and Diamond Blackfan AnemiaP20GM121293 · NIGMS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI Samrat Roy Choudhury · 2017 to 2026
$27.6M
Study of the Cell-specific Inflammasome Responses During Defense Against Gram-negative BacteriaP20GM103625 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI SMELTZER, MARK S · 2012 to 2021
$21.5M
Arkansas Center for Clinical and Translational ResearchUL1TR000039 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI BECK, CORNELIA MARIE, JAMES, LAURA P · 2012 to 2014
$10.0M
Biochemistry of recombination in meiosisR01GM081766 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI WAHLS, WAYNE P · 2007 to 2018
$2.5M
Impact of ethanol-induced protein nitration on the histone modification codeR21AA022185 · NIAAA · UNIVERSITY OF SOUTH FLORIDA · PI STEVENS, STANLEY M · 2014 to 2015
$380k
Role of PHPT1 in oxidative stress-induced epigenetic modifications by ethanolR21AA021247 · NIAAA · UNIVERSITY OF SOUTH FLORIDA · PI STEVENS, STANLEY M · 2013 to 2014
$379k
NIAAA NIH HHS R21 AA021247NIAAA NIH HHS R21 AA022185NIGMS NIH HHS P20 GM103429NIGMS NIH HHS P20 GM103625NIGMS NIH HHS P20 GM121293NIGMS NIH HHS R01 GM081766
6 · The paper itself

Abstract

backgroundEpigenetic dysregulation through ethanol (EtOH)-induced changes in DNA methylation and histone modifications has been implicated in several alcohol-related disorders such as alcoholic liver disease. EtOH metabolism in the liver results in the formation of acetate, a metabolite that can be converted to acetyl-CoA, which can then be used by histone acetyltransferases to acetylate lysine residues. EtOH metabolism in the liver can also indirectly influence lysine acetylation through NAD

methodsEight-week-old male C57BL/6J mice were gavaged using a bolus dose of either

resultsData show significant incorporation of the EtOH-derived

conclusionsThese data provide the first quantitative evidence of how hepatic EtOH metabolism directly influences histone lysine acetylation in a site-specific manner and may influence EtOH-induced gene expression through these transcriptionally activating chromatin marks.

Indexed as

AcetylationAlcohol DrinkingAnimalsEthanolHistonesLiverMaleMiceMice, Inbred C57BLEthanolHistonesAlcohol Liver DiseaseEpigeneticsHepatocytesHistone AcetylationMetabolic Tracing

Identifiers

PMID30030934
PMCPMC6208134
OpenAlexW2884380558

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.