Evidence map›Paper›PMID 25252616›Full record

ReviewExpert opinion on drug metabolism & toxicology2014

Pregnane X receptor and drug-induced liver injury.

Yue-Ming Wang, Sergio C Chai, Christopher T Brewer, Taosheng Chen

Abstract readReview
In one paragraph

Review in Expert opinion on drug metabolism & toxicology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.3field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
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  4. Article
  5. Review
  6. Article
  7. Drug metabolism and disposition: the biological fate of chemicals · 2022
    Article
  8. Review
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  12. Review
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  18. The Isoniazid Metabolites Hydrazine and Pyridoxal Isonicotinoyl Hydrazone Modulate Heme Biosynthesis.Toxicological sciences : an official journal of the Society of Toxicology · 2019
    Article
  19. Review
  20. 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

4 authors at 2 institutions in 1 country.

Yue-Ming WangSt. Jude Children's Research Hospital, Department of Chemical Biology and Therapeutics , 262 Danny Thomas Place, Memphis, TN 38105 , USA.
Sergio C Chai
Christopher T Brewer
Taosheng Chen
St. Jude Children's Research Hospital · USUniversity of Tennessee Health Science Center · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Regulation of PXR by cell cycle and phosphorylationR01GM086415 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHEN, TAOSHENG · 2010 to 2013
$1.3M
Regulation of drug disposition by a novel microRNA-mediated pathwayR01GM110034 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHEN, TAOSHENG · 2014 to 2016
$998k
NCI NIH HHS P30 CA021765NCI NIH HHS P30-CA21765NIGMS NIH HHS GM086415NIGMS NIH HHS GM110034NIGMS NIH HHS R01 GM086415NIGMS NIH HHS R01 GM110034
6 · The paper itself

Abstract

introductionThe liver plays a central role in transforming and clearing foreign substances. The continuous exposure of the liver to xenobiotics sometimes leads to impaired liver function, referred to as drug-induced liver injury (DILI). The pregnane X receptor (PXR) tightly regulates the expression of genes in the hepatic drug-clearance system and its undesired activation plays a role in DILI. AREAS COVERED: This review focuses on the recent progress in understanding PXR-mediated DILI and highlights the efforts made to assess and manage PXR-mediated DILI during drug development. EXPERT OPINION: Future efforts are needed to further elucidate the mechanisms of PXR-mediated liver injury, including the epigenetic regulation and polymorphisms of PXR. Novel in vitro models containing functional PXR could improve our ability to predict and assess DILI during drug development. PXR inhibitors may provide chemical tools to validate the potential of PXR as a therapeutic target and to develop drugs to be used in the clinic to manage PXR-mediated DILI.

Indexed as

AnimalsChemical and Drug Induced Liver InjuryDrug DesignEpigenesis, GeneticGene Expression RegulationHumansLiverPolymorphism, GeneticPregnane X ReceptorReceptors, SteroidXenobioticsPregnane X ReceptorReceptors, SteroidXenobioticsadverse drug reactiondrug-induced liver injurypregnane X receptorxenobiotic detoxificationxenobiotic receptor

Identifiers

PMID25252616
PMCPMC4198438
OpenAlexW2103281358

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.