Evidence map›Paper›PMID 30149019›Full record

ArticleBiochemical pharmacology2018

Expression and genotype-dependent catalytic activity of N-acetyltransferase 2 (NAT2) in human peripheral blood mononuclear cells and its modulation by Sirtuin 1.

Raúl A Salazar-González, Eneida Turiján-Espinoza, David W Hein, Rosa C Milán-Segovia, Edith E Uresti-Rivera, Diana P Portales-Pérez

Open access · greenAbstract read
In one paragraph

Article in Biochemical pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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  3. Article
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  5. Article
  6. ArylamineFrontiers in pharmacology · 2022
    Article
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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 2 countries.

Raúl A Salazar-GonzálezTranslational and Molecular Medicine Department, Research Center for Health Sciences and Biomedicine, Autonomous University of San Luis Potosí, Mexico; Department of Pharmacology and Toxicology and James Graham Brown Cancer Center, University of Louisville, USA.
Eneida Turiján-EspinozaTranslational and Molecular Medicine Department, Research Center for Health Sciences and Biomedicine, Autonomous University of San Luis Potosí, Mexico; Chemical Sciences School, Autonomous University of San Luis Potosí, Mexico.
David W HeinDepartment of Pharmacology and Toxicology and James Graham Brown Cancer Center, University of Louisville, USA.
Rosa C Milán-SegoviaChemical Sciences School, Autonomous University of San Luis Potosí, Mexico.
Edith E Uresti-RiveraTranslational and Molecular Medicine Department, Research Center for Health Sciences and Biomedicine, Autonomous University of San Luis Potosí, Mexico; Chemical Sciences School, Autonomous University of San Luis Potosí, Mexico.
Diana P Portales-PérezTranslational and Molecular Medicine Department, Research Center for Health Sciences and Biomedicine, Autonomous University of San Luis Potosí, Mexico; Chemical Sciences School, Autonomous University of San Luis Potosí, Mexico. Electronic address: dportale@uaslp.mx.
Autonomous University of San Luis Potosí · MXUniversity of Louisville · US

Funding

Role of oxidized linoleic acid metabolites in the pathogenesis of alcoholic liver diseaseP20GM113226 · NIGMS · UNIVERSITY OF LOUISVILLE · PI MCCLAIN, CRAIG J. · 2016 to 2025
$24.1M
The Role of Nutrition in the Development/Progression of Alcohol-Induced Organ InjuryP50AA024337 · NIAAA · UNIVERSITY OF LOUISVILLE · PI CRAIG J. MCCLAIN · 2016 to 2026
$17.9M
NIAAA NIH HHS P50 AA024337NIGMS NIH HHS P20 GM113226
6 · The paper itself

Abstract

N-acetyltransferase 2 (NAT2) catalyzes the biotransformation of numerous arylamine and hydrazine drugs and carcinogens. Genetic polymorphisms of NAT2 modify drug efficacy and toxicity and susceptibility to diseases such as cancer and type 2 diabetes. Expression of NAT2 has been documented in the liver and gastrointestinal tract but not in other tissues. Deacetylation of cytosolic proteins by sirtuins is a post-translational modification important in regulatory networks of diverse cellular processes. The aim of the present study was to investigate NAT2 expression in peripheral blood mononuclear cells (PBMC) and the effects of NAT2 genotype and Sirtuin 1 (SIRT1). Both NAT2 and SIRT1 proteins were expressed on PBMC. Their expression was more prevalent on CD3+ compared to CD19+ and CD56+ cell populations. N-acetylation capacity of PBMC exhibited a NAT2 gene-dose response toward the N-acetylation of isoniazid. Subjects with rapid NAT2 genotype showed an apparent V

Indexed as

GenotypeAdultArylamine N-AcetyltransferaseFemaleGene Expression RegulationHumansIsoniazidLeukocytes, MononuclearMaleRNA, MessengerSirtuin 1Young AdultArylamine N-AcetyltransferaseIsoniazidNAT2 protein, humanRNA, MessengerSIRT1 protein, humanSirtuin 1Acetylator phenotypeN-acetyltransferase 2Peripheral blood mononuclear cellsPost-translational modificationsSirtuin 1

Identifiers

PMID30149019
PMCPMC6350916
OpenAlexW2888631579

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.