Evidence map›Paper›PMID 27085140›Full record

ArticleBiochimica et biophysica acta2016

MicroRNA-30c-1-3p is a silencer of the pregnane X receptor by targeting the 3'-untranslated region and alters the expression of its target gene cytochrome P450 3A4.

Thaveechai Vachirayonstien, Bingfang Yan

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Circulating miRNAs as Biomarkers for CYP2B6 Enzyme Activity.Clinical pharmacology and therapeutics · 2021
    Article
  6. Review
  7. Review
  8. Article
  9. Regulation of cytochrome P450 expression by microRNAs and long noncoding RNAs: Epigenetic mechanisms in environmental toxicology and carcinogenesis.Journal of environmental science and health. Part C, Environmental carcinogenesis & ecotoxicology reviews · 2019
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. 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

2 authors at 1 institution in 1 country.

Thaveechai VachirayonstienDepartment of Biomedical and Pharmaceutical Sciences, Center for Integrated Drug Development, University of Rhode Island, Kingston, RI 02881, United States.
Bingfang YanDepartment of Biomedical and Pharmaceutical Sciences, Center for Integrated Drug Development, University of Rhode Island, Kingston, RI 02881, United States. Electronic address: byan@uri.edu.
University of Rhode Island · US

Funding

Signaling of the Pregnane X ReceptorR01GM061988 · NIGMS · UNIVERSITY OF RHODE ISLAND · PI DENG, RUITANG · 2000 to 2016
$3.0M
Molecular Toxicology of CarboxylesterasesR01ES007965 · NIEHS · UNIVERSITY OF RHODE ISLAND · PI YAN, BINGFANG · 2003 to 2006
$1.2M
Interplay between metabolism and FXR activation in scoparone signalingR15AT007705 · NCCIH · UNIVERSITY OF RHODE ISLAND · PI YAN, BINGFANG · 2013 to 2013
$437k
NCCIH NIH HHS R15 AT007705NIEHS NIH HHS R01 ES007965NIGMS NIH HHS R01 GM061988
6 · The paper itself

Abstract

The pregnane X receptor (PXR) is a master regulator of genes involved in drug elimination. Recently, activation of PXR has also been linked to the development of many disease conditions such as metabolic disorders and malignancies. MicroRNAs (miRs) emerge as important molecular species involved in these conditions. This study was undertaken to test a large number of miRs for their ability to regulate PXR expression. As many as 58 miRs were tested and miR-30c-1-3p was identified to suppress PXR expression. The suppression was achieved by targeting the 3'-untranslated region, 438 nucleotides from the stop codon. The suppression was detected in multiple cell lines from different organ origins. In addition, miR-30c-1-3p altered basal and induced expression of cytochrome P450 3A4 (CYP3A4), a prototypical target gene of PXR. The alteration varied depending on the time and amounts of miR-30c-1-3p. CYP3A4 is responsible for the metabolism of more than 50% medicines. The interconnection between miR-30c-1-3p and PXR signifies a role of miRs in drug-drug interactions and chemosensitivity. This article is part of a Special Issue entitled: Xenobiotic nuclear receptors: New Tricks for An Old Dog, edited by Dr. Wen Xie.

Indexed as

3' Untranslated RegionsGene Expression RegulationBase SequenceCell Line, TumorCytochrome P-450 CYP3AEpithelial CellsGenes, ReporterHEK293 CellsHep G2 CellsHumansLuciferasesMicroRNAsPlasmidsPregnane X ReceptorReceptors, SteroidSignal Transduction3' Untranslated RegionsCYP3A4 protein, humanCytochrome P-450 CYP3ALuciferasesMicroRNAsMIRN30b microRNA, humanPregnane X ReceptorReceptors, SteroidChemosensitivityDrug–drug interactionMicroRNA CYP3A4Nuclear receptorPXR

Identifiers

PMID27085140
PMCPMC4975670
OpenAlexW2336361053

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.