Evidence map›Paper›PMID 24551047›Full record

ArticlePloS one2014

Multiple tumor suppressor microRNAs regulate telomerase and TCF7, an important transcriptional regulator of the Wnt pathway.

Radmila Hrdličková, Jiří Nehyba, William Bargmann, Henry R Bose

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Role of telomere length in human carcinogenesis (Review).International journal of oncology · 2023
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Genes · 2021
    Article
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  16. Article
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  20. Observational
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.

Radmila HrdličkováDepartment of Molecular Biosciences, College of Natural Sciences, and Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, United States of America.
Jiří NehybaDepartment of Molecular Biosciences, College of Natural Sciences, and Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, United States of America.
William BargmannDepartment of Molecular Biosciences, College of Natural Sciences, and Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, United States of America.
Henry R BoseDepartment of Molecular Biosciences, College of Natural Sciences, and Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, United States of America.
The University of Texas at Austin · US

Funding

Transformation by Reticuloendotheliosis VirusR01CA033192 · NCI · UNIVERSITY OF TEXAS AUSTIN · PI BOSE, HENRY R · 1985 to 2011
$3.0M
Mechanism of oncogenesis by Rel/NF-kappaBR01CA098151 · NCI · UNIVERSITY OF TEXAS AUSTIN · PI BOSE, HENRY R · 2003 to 2007
$1.5M
NCI NIH HHS CA098151NCI NIH HHS CA33192NCI NIH HHS R01 CA033192NCI NIH HHS R01 CA098151
6 · The paper itself

Abstract

The human TERT (hTERT) gene encodes the telomerase catalytic subunit which plays a role in telomerase regulation. Telomerase is activated in more than 90% of all human malignancies and understanding how telomerase is regulated is necessary for implementation of successful anti-cancer therapies. microRNAs (miRNAs) are important regulators of gene expression in eukaryotic cells but evidence of their role in telomerase regulation has not been documented. To determine whether hTERT activity is regulated by multiple miRNAs, eight miRNAs which have putative binding sites in the hTERT 3'UTR together with miR-138-5p were evaluated in luciferase assays with a reporter containing the hTERT 3'UTR. Six miRNAs (let-7g*, miR-133a, miR-138-5p, miR-342-5p, miR-491-5p, and miR-541-3p) specifically inhibited the expression of the reporter luciferase-driven constructs and let-7g*, miR-133a, miR-138-5p, and miR-491-5p also downregulated endogenous telomerase activity in cells. Moreover, all six miRNAs significantly inhibited cell proliferation. miRNAs (miR-133a, miR-138-5p, 342-5p, 491-5p, 541-3p) also have predicted binding sites within the 3'UTR of three genes involved in Wnt signaling (TCF7, MSI1, and PAX5). These miRNAs inhibited the expression of the luciferase reporter constructs containing 3'UTRs of these genes and downregulated protein expression of the TCF7 transcription factor, which mediates the canonical Wnt pathway. Together, these results suggest the existence of a miRNA regulatory network involving the hTERT and Wnt pathway.

Indexed as

Genes, Tumor SuppressorTranscription, Genetic3' Untranslated RegionsCell Line, TumorCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticGenes, ReporterHumansLuciferasesMicroRNAsNerve Tissue ProteinsPAX5 Transcription FactorRNA-Binding ProteinsT Cell Transcription Factor 1Telomerase3' Untranslated RegionsLuciferasesMicroRNAsMSI1 protein, humanNerve Tissue ProteinsPAX5 protein, humanPAX5 Transcription FactorRNA-Binding ProteinsT Cell Transcription Factor 1TCF7 protein, humanTelomeraseTERT protein, human

Identifiers

PMID24551047
PMCPMC3925088
OpenAlexW2113834894

What OpenQuestion holds

Textmetadata
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.