Evidence map›Paper›PMID 21603612›Full record

ArticlePloS one2011

NFATc1 regulation of TRAIL expression in human intestinal cells.

Qingding Wang, Yuning Zhou, Heidi L Weiss, Chi-Wing Chow, B Mark Evers

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. NFAT gene family in inflammation and cancer.Current molecular medicine · 2013
    Review
  11. Article
  12. Regulation of the human TRAIL gene.Cancer biology & therapy · 2012
    Review
  13. 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

5 authors at 3 institutions in 1 country.

Qingding WangDepartment of Surgery, The University of Kentucky, Lexington, Kentucky, United States of America.
Yuning Zhou
Heidi L Weiss
Chi-Wing Chow
B Mark Evers
Markey Cancer Center · USAlbert Einstein College of Medicine · USUniversity of Kentucky · US

Funding

SURGICAL STUDIES OF FUNCTIONAL GENE EXPRESSIONR01DK048498 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI EVERS, BERNARD MARK · 1996 to 2023
$7.9M
Molecular Signaling in AdipocytesR01DK090481 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CHOW, CHI-WING · 2011 to 2014
$1.5M
UK SPORE in Gastrointestinal CancerP20CA150343 · NCI · UNIVERSITY OF KENTUCKY · PI EVERS, BERNARD MARK · 2009 to 2011
$1.5M
NCI NIH HHS P20 CA150343NCI NIH HHS P20CA150343NIDDK NIH HHS R01 DK048498NIDDK NIH HHS R01 DK090481
6 · The paper itself

Abstract

TNF-related apoptosis-inducing ligand (TRAIL; Apo2) has been shown to promote intestinal cell differentiation. Nuclear factor of activated T cells (NFAT) participates in the regulation of a variety of cellular processes, including differentiation. Here, we examined the role of NFAT in the regulation of TRAIL in human intestinal cells. Treatment with a combination of phorbol 12-myristate 13-acetate (PMA) plus the calcium ionophore A23187 (Io) increased NFAT activation and TRAIL expression; pretreatment with the calcineurin inhibitor cyclosporine A (CsA), an antagonist of NFAT signaling, diminished NFAT activation and TRAIL induction. In addition, knockdown of NFATc1, NFATc2, NFATc3, and NFATc4 blocked PMA/Io increased TRAIL protein expression. Expression of NFATc1 activated TRAIL promoter activity and increased TRAIL mRNA and protein expression. Deletion of NFAT binding sites from the TRAIL promoter did not significantly abrogate NFATc1-increased TRAIL promoter activity, suggesting an indirect regulation of TRAIL expression by NFAT activation. Knockdown of NFATc1 increased Sp1 transcription factor binding to the TRAIL promoter and, importantly, inhibition of Sp1, by chemical inhibition or RNA interference, increased TRAIL expression. These studies identify a novel mechanism for TRAIL regulation by which activation of NFATc1 increases TRAIL expression through negative regulation of Sp1 binding to the TRAIL promoter.

Indexed as

Gene Expression RegulationCells, CulturedHumansIntestinal MucosaIntestinesNFATC Transcription FactorsPromoter Regions, GeneticProtein BindingRNA, MessengerSp1 Transcription FactorTNF-Related Apoptosis-Inducing LigandNFATC1 protein, humanNFATC Transcription FactorsRNA, MessengerSp1 Transcription FactorTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, human

Identifiers

PMID21603612
PMCPMC3095616
OpenAlexW2101541382

What OpenQuestion holds

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LicenceCC BY
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.