Evidence map›Paper›PMID 21592959›Full record

ArticleThe Journal of biological chemistry2011

Usp18 regulates epidermal growth factor (EGF) receptor expression and cancer cell survival via microRNA-7.

Jason E Duex, Laurey Comeau, Alexander Sorkin, Benjamin Purow, Benjamin Kefas

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Molecular mechanism of theAnnals of translational medicine · 2023
    Article
  5. Msi2-mediated MiR7a-1 processing repression promotes myogenesis.Journal of cachexia, sarcopenia and muscle · 2022
    Article
  6. Article
  7. Review
  8. Deubiquitinases: Modulators of Different Types of Regulated Cell Death.International journal of molecular sciences · 2021
    Review
  9. MiR-7 in Cancer Development.Biomedicines · 2021
    Review
  10. Review
  11. Emerging Roles of USP18: From Biology to Pathophysiology.International journal of molecular sciences · 2020
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. The role of deubiquitinases in breast cancer.Cancer metastasis reviews · 2016
    Review
  19. Multiple functions of USP18.Cell death & disease · 2016
    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

5 authors at 2 institutions in 1 country.

Jason E DuexDepartment of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, USA.
Laurey Comeau
Alexander Sorkin
Benjamin Purow
Benjamin Kefas
University of Virginia Health System · USUniversity of Pittsburgh · US

Funding

PATHOGENESIS OF CANCER--ROLE OF EGF RECEPTOR ENDOCYTOSISR01CA089151 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SORKIN, ALEXANDER D · 2001 to 2023
$6.9M
Investigation of Notch-inhibiting microRNAs in gliomaR01CA136803 · NCI · UNIVERSITY OF VIRGINIA · PI PUROW, BENJAMIN W. · 2009 to 2013
$1.5M
Novel Negative Regulators of EGF Receptor DownregulationF32CA126344 · NCI · UNIVERSITY OF COLORADO DENVER · PI DUEX, JASON E. · 2006 to 2008
$145k
Howard Hughes Medical InstituteNCI NIH HHS F32 CA126344NCI NIH HHS F32CA126344NCI NIH HHS R01 CA089151NCI NIH HHS R01 CA136803
6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) is involved in development and progression of many human cancers. We have previously demonstrated that the ubiquitin-specific peptidase Usp18 (Ubp43) is a potent regulator of EGFR protein expression. Here we report that the 3'-untranslated region (3'-UTR) of the EGFR message modulates RNA translation following cell treatment with Usp18 siRNA, suggesting microRNA as a possible mediator. Given earlier evidence of EGFR regulation by the microRNA miR-7, we assessed whether miR-7 mediates Usp18 siRNA effects. We found that Usp18 depletion elevates miR-7 levels in several cancer cell lines because of a transcriptional activation and/or mRNA stabilization of miR-7 host genes and that miR-7 acts downstream of Usp18 to regulate EGFR mRNA translation via the 3'-UTR. Also, depletion of Usp18 led to a decrease in protein levels of other known oncogenic targets of miR-7, reduced cell proliferation and soft agar colony formation, and increased apoptosis. Notably, all of these phenotypes were reversed by a specific inhibitor of miR-7. Thus, our findings support a model in which Usp18 inhibition promotes up-regulation of miR-7, which in turn inhibits EGFR expression and the tumorigenic activity of cancer cells.

Indexed as

3' Untranslated RegionsGene Expression Regulation, NeoplasticModels, BiologicalApoptosisCell ProliferationEndopeptidasesErbB ReceptorsGene Knockdown TechniquesHeLa CellsHumansMicroRNAsNeoplasm ProteinsNeoplasmsRNA, NeoplasmRNA StabilityUbiquitin Thiolesterase3' Untranslated RegionsEGFR protein, humanEndopeptidasesErbB ReceptorsMicroRNAsMIRN7-1 microRNA, humanNeoplasm ProteinsRNA, NeoplasmUbiquitin ThiolesteraseUSP18 protein, human

Identifiers

PMID21592959
PMCPMC3137108
OpenAlexW2049260350

What OpenQuestion holds

Textmetadata
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.