Evidence map›Paper›PMID 23330541›Full record

ReviewDrug metabolism reviews2013

Nuclear-receptor-mediated regulation of drug- and bile-acid-transporter proteins in gut and liver.

Jeff L Staudinger, Sarah Woody, Mengxi Sun, Wenqi Cui

Open access · greenAbstract readReview
In one paragraph

Review in Drug metabolism reviews, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Novel Techniques and Models for Studying the Role of the Gut Microbiota in Drug Metabolism.European journal of drug metabolism and pharmacokinetics · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Drug metabolism and disposition: the biological fate of chemicals · 2022
    Article
  12. Role of Bile Acids and Nuclear Receptors in Acupuncture in Improving Crohn's Disease.Evidence-based complementary and alternative medicine : eCAM · 2022
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study.Toxicology in vitro : an international journal published in association with BIBRA · 2019
    Article
  20. 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.

Jeff L StaudingerDepartment of Pharmacology and Toxicology, University of Kansas, Lawrence, Kansas 66045, USA. stauding@ku.edu
Sarah Woody
Mengxi Sun
Wenqi Cui
University of Kansas · US

Funding

Inflammation, PXR Modification and Drug DispositionR01DK090558 · NIDDK · UNIVERSITY OF KANSAS LAWRENCE · PI STAUDINGER, JEFFREY L · 2011 to 2014
$1.3M
NIDDK NIH HHS R01 DK090558
6 · The paper itself

Abstract

Adverse drug events (ADEs) are a common cause of patient morbidity and mortality and are classically thought to result, in part, from variation in expression and activity of hepatic enzymes of drug metabolism. It is now known that alterations in the expression of genes that encode drug- and bile-acid-transporter proteins in both the gut and liver play a previously unrecognized role in determining patient drug response and eventual clinical outcome. Four nuclear receptor (NR) superfamily members, including pregnane X receptor (PXR, NR1I2), constitutive androstane receptor (NR1I3), farnesoid X receptor (NR1H4), and vitamin D receptor (NR1I1), play pivotal roles in drug- and bile-acid-activated programs of gene expression to coordinately regulate drug- and bile-acid transport activity in the intestine and liver. This review focuses on the NR-mediated gene activation of drug and bile-acid transporters in these tissues as well as the possible underlying molecular mechanisms.

Indexed as

AnimalsBile Acids and SaltsBiological TransportCarrier ProteinsConstitutive Androstane ReceptorGastrointestinal TractHumansInactivation, MetabolicLiverMembrane GlycoproteinsReceptors, Cytoplasmic and Nuclearbile acid binding proteinsBile Acids and SaltsCarrier ProteinsConstitutive Androstane ReceptorMembrane GlycoproteinsNR1I3 protein, humanReceptors, Cytoplasmic and Nuclear

Identifiers

PMID23330541
PMCPMC4557796
OpenAlexW2067961925

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.