Evidence map›Paper›PMID 29240439›Full record

ArticleMolecular pharmaceutics2018

Defining Metabolic and Nonmetabolic Regulation of Histone Acetylation by NSAID Chemotypes.

Jonathan H Shrimp, Julie M Garlick, Tugsan Tezil, Alexander W Sorum, Andrew J Worth, Ian A Blair, Eric Verdin, Nathaniel W Snyder, Jordan L Meier

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 9 citations in OpenAlex.

  1. Epigenetic regulation by endogenous metabolite pharmacology.Current opinion in chemical biology · 2019
    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.

Jonathan H ShrimpChemical Biology Laboratory , National Cancer Institute , Frederick , Maryland 21702 , United States.ORCID 0000-0001-9872-942X
Julie M GarlickChemical Biology Laboratory , National Cancer Institute , Frederick , Maryland 21702 , United States.
Tugsan TezilBuck Institute for Research on Aging, Novato , California 94945 , United States.
Alexander W SorumChemical Biology Laboratory , National Cancer Institute , Frederick , Maryland 21702 , United States.
Andrew J WorthPenn SRP Center, Center of Excellence in Environmental Toxicology , University of Pennsylvania , Philadelphia Pennsylvania 19104 , United States.
Ian A BlairPenn SRP Center, Center of Excellence in Environmental Toxicology , University of Pennsylvania , Philadelphia Pennsylvania 19104 , United States.
Eric VerdinBuck Institute for Research on Aging, Novato , California 94945 , United States.
Nathaniel W SnyderDrexel University, A.J. Drexel Autism Institute , 3020 Market Street , Philadelphia Pennsylvania 19104 , United States.
Jordan L MeierChemical Biology Laboratory , National Cancer Institute , Frederick , Maryland 21702 , United States.ORCID 0000-0002-0537-7101
Frederick National Laboratory for Cancer Research · USBuck Institute for Research on Aging · USUniversity of Pennsylvania · USDrexel University · US

Funding

Targeting Cancer Through Modifications and MetabolismZIABC011488 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MEIER, JORDAN L · 2013 to 2025
$21.3M
Intramural NIH HHS ZIA BC011488
6 · The paper itself

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) are well-known for their effects on inflammatory gene expression. Although NSAIDs are known to impact multiple cellular signaling mechanisms, a recent finding is that the NSAID salicylate can disrupt histone acetylation, in part through direct inhibition of the lysine acetyltransferase (KAT) p300/CBP. While salicylate is a relatively weak KAT inhibitor, its CoA-linked metabolite is more potent; however, the ability of NSAID metabolites to inhibit KAT enzymes biochemically and in cells remains relatively unexplored. Here we define the role of metabolic and nonmetabolic mechanisms in inhibition of KAT activity by NSAID chemotypes. First, we screen a small panel of NSAIDs for biochemical inhibition of the prototypical KAT p300, leading to the finding that many carboxylate-containing NSAIDs, including ibuprofen, are able to function as weak inhibitors. Assessing the inhibition of p300 by ibuprofen-CoA, a known NSAID metabolite, reveals that linkage of ibuprofen to CoA increases its biochemical potency toward p300 and other KAT enzymes. In cellular studies, we find that carboxylate-containing NSAIDs inhibit histone acetylation. Finally, we exploit the stereoselective metabolism of ibuprofen to assess the role of its acyl-CoA metabolite in regulation of histone acetylation. This unique strategy reveals that formation of ibuprofen-CoA and histone acetylation are poorly correlated, suggesting metabolism may not be required for ibuprofen to inhibit histone acetylation. Overall, these studies provide new insights into the ability of NSAIDs to alter histone acetylation, and illustrate how selective metabolism may be leveraged as a tool to explore the influence of metabolic acyl-CoAs on cellular enzyme activity.

Indexed as

AcetylationAcyl Coenzyme AAnti-Inflammatory Agents, Non-SteroidalE1A-Associated p300 ProteinEnzyme AssaysGene Expression RegulationHEK293 CellsHistone CodeHistonesHumansMetabolic Networks and PathwaysProtein Processing, Post-TranslationalRecombinant ProteinsAcyl Coenzyme AAnti-Inflammatory Agents, Non-SteroidalE1A-Associated p300 ProteinEP300 protein, humanHistonesRecombinant ProteinsacetylationepigeneticsibuprofeninflammationNSAIDs

Identifiers

PMID29240439
PMCPMC6320251
OpenAlexW2775114294

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.