Evidence map›Paper›PMID 24135829›Full record

ArticleLeukemia2014

A role for eukaryotic initiation factor 4B overexpression in the pathogenesis of diffuse large B-cell lymphoma.

E Horvilleur, T Sbarrato, K Hill, R V Spriggs, M Screen, P J Goodrem, K Sawicka, L C Chaplin, C Touriol, G Packham and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. PARK2 regulates eIF4B-driven lymphomagenesis.Molecular cancer research : MCR · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Role of RONS and eIFs in Cancer Progression.Oxidative medicine and cellular longevity · 2021
    Review
  18. Article
  19. Article
  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

17 authors at 7 institutions in 4 countries.

E HorvilleurMedical Research Council Toxicology Unit, Leicester, UK.
T SbarratoMedical Research Council Toxicology Unit, Leicester, UK.
K HillMedical Research Council Toxicology Unit, Leicester, UK.
R V SpriggsMedical Research Council Toxicology Unit, Leicester, UK.
M ScreenMedical Research Council Toxicology Unit, Leicester, UK.
P J GoodremMedical Research Council Toxicology Unit, Leicester, UK.
K SawickaMedical Research Council Toxicology Unit, Leicester, UK.
L C ChaplinMedical Research Council Toxicology Unit, Leicester, UK.
C TouriolINSERM UMR 1037-CRCT-Equipe 5 CHU Rangueil Toulouse, France.
G PackhamFaculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK.
K N PotterFaculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK.
S DirnhoferInstitute of Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.
A TzankovInstitute of Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.
M J S DyerMedical Research Council Toxicology Unit, Leicester, UK.
M BushellMedical Research Council Toxicology Unit, Leicester, UK.
M MacFarlaneMedical Research Council Toxicology Unit, Leicester, UK.
A E WillisMedical Research Council Toxicology Unit, Leicester, UK.
Medical Research Council · GBUniversity of Southampton · GBAlbert Einstein College of Medicine · USBabraham Institute · GBInserm · FRUniversity Hospital of Basel · CHUniversity of Basel · CH

Funding

British Heart FoundationMedical Research Council MC_U132685863Medical Research Council MC_UP_A600_1023Medical Research Council MC_UP_A600_1024
6 · The paper itself

Abstract

Dysregulated expression of factors that control protein synthesis is associated with poor prognosis of many cancers, but the underlying mechanisms are not well defined. Analysis of the diffuse large B-cell lymphoma (DLBCL) translatome revealed selective upregulation of mRNAs encoding anti-apoptotic and DNA repair proteins. We show that enhanced synthesis of these proteins in DLBCL is mediated by the relief of repression that is normally imposed by structure in the 5'-untranslated regions of their corresponding mRNAs. This process is driven by signaling through mammalian target of rapamycin, resulting in increased synthesis of eukaryotic initiation factor (eIF) 4B complex (eIF4B), a known activator of the RNA helicase eIF4A. Reducing eIF4B expression alone is sufficient to decrease synthesis of proteins associated with enhanced tumor cell survival, namely DAXX, BCL2 and ERCC5. Importantly, eIF4B-driven expression of these key survival proteins is directly correlated with patient outcome, and eIF4B, DAXX and ERCC5 are identified as novel prognostic markers for poor survival in DLBCL. Our work provides new insights into the mechanisms by which the cancer-promoting translational machinery drives lymphomagenesis.

Indexed as

5' Untranslated RegionsCell Line, TumorElectrophoresis, Polyacrylamide GelEukaryotic Initiation FactorsHumansLymphoma, Large B-Cell, DiffuseOligonucleotide Array Sequence AnalysisReverse Transcriptase Polymerase Chain ReactionRNA, MessengerUp-Regulation5' Untranslated RegionseIF-4BEukaryotic Initiation FactorsRNA, Messenger

Identifiers

PMID24135829
PMCPMC4017261
OpenAlexW1991312668

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.