Evidence map›Paper›PMID 25986608›Full record

ArticleMolecular and cellular biology2015

Eukaryotic Translation Initiation Factor 4E Is a Feed-Forward Translational Coactivator of Transforming Growth Factor β Early Protransforming Events in Breast Epithelial Cells.

Lindsey Decarlo, Celine Mestel, Mary-Helen Barcellos-Hoff, Robert J Schneider

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Translation initiation factors and their relevance in cancer.Current opinion in genetics & development · 2018
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Adaptations to chronic rapamycin in mice.Pathobiology of aging & age related diseases · 2016
    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

4 authors at 1 institution in 1 country.

Lindsey DecarloDepartment of Microbiology, New York University School of Medicine, New York, New York, USA.
Celine MestelDepartment of Microbiology, New York University School of Medicine, New York, New York, USA.
Mary-Helen Barcellos-HoffDepartment of Radiation Oncology, New York University School of Medicine, New York, New York, USA NYU Cancer Institute, New York University School of Medicine, New York, New York, USA.
Robert J SchneiderDepartment of Microbiology, New York University School of Medicine, New York, New York, USA Department of Radiation Oncology, New York University School of Medicine, New York, New York, USA NYU Cancer Institute, New York University School of Medicine, New York, New York, USA Robert.schneider@nyumc.org.
New York University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
NCI NIH HHS P30 CA016087
6 · The paper itself

Abstract

Eukaryotic translation initiation factor 4E (eIF4E) is overexpressed early in breast cancers in association with disease progression and reduced survival. Much remains to be understood regarding the role of eIF4E in human cancer. We determined, using immortalized human breast epithelial cells, that elevated expression of eIF4E translationally activates the transforming growth factor β (TGF-β) pathway, promoting cell invasion, a loss of cell polarity, increased cell survival, and other hallmarks of early neoplasia. Overexpression of eIF4E is shown to facilitate the selective translation of integrin β1 mRNA, which drives the translationally controlled assembly of a TGF-β receptor signaling complex containing α3β1 integrins, β-catenin, TGF-β receptor I, E-cadherin, and phosphorylated Smad2/3. This receptor complex acutely sensitizes nonmalignant breast epithelial cells to activation by typically substimulatory levels of activated TGF-β. TGF-β can promote cellular differentiation or invasion and transformation. As a translational coactivator of TGF-β, eIF4E confers selective mRNA translation, reprogramming nonmalignant cells to an invasive phenotype by reducing the set point for stimulation by activated TGF-β. Overexpression of eIF4E may be a proinvasive facilitator of TGF-β activity.

Indexed as

beta CateninBreast NeoplasmsCadherinsCell Line, TumorCell ProliferationCell Transformation, NeoplasticEpithelial CellsEukaryotic Initiation Factor-4EFemaleHumansIntegrin alpha3beta1Integrin beta1Neoplasm InvasivenessPhosphorylationReceptors, Transforming Growth Factor betaRNA Interferencebeta CateninCadherinsEukaryotic Initiation Factor-4EIntegrin alpha3beta1Integrin beta1Receptors, Transforming Growth Factor betaRNA, Small InterferingSmad2 ProteinSMAD2 protein, humanSmad3 ProteinSMAD3 protein, humanTransforming Growth Factor beta

Identifiers

PMID25986608
PMCPMC4524117
OpenAlexW2269266363

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.