Evidence map›Paper›PMID 21075834›Full record

ArticleHuman molecular genetics2011

Drosophila orthologue of WWOX, the chromosomal fragile site FRA16D tumour suppressor gene, functions in aerobic metabolism and regulates reactive oxygen species.

Louise V O'Keefe, Alex Colella, Sonia Dayan, Qingwen Chen, Amanda Choo, Reuben Jacob, Gareth Price, Deon Venter, Robert I Richards

Open access · bronzeAbstract read
In one paragraph

Article in Human molecular genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

46 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Alzheimer's disease risk geneBrain communications · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Endothelial knockdown of the tumor suppressor,American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  7. Loss of fragile WWOX gene leads to senescence escape and genome instability.Cellular and molecular life sciences : CMLS · 2023
    Article
  8. WWOX and metabolic regulation in normal and pathological conditions.Journal of molecular medicine (Berlin, Germany) · 2022
    Review
  9. Article
  10. TheInternational journal of molecular sciences · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Investigating Developmental and Epileptic Encephalopathy UsingInternational journal of molecular sciences · 2020
    Review
  17. TheExperimental biology and medicine (Maywood, N.J.) · 2020
    Review
  18. Review
  19. How DNA methylation affects the Warburg effect.International journal of biological sciences · 2020
    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

9 authors at 2 institutions in 2 countries.

Louise V O'KeefeARC Special Research Centre for the Molecular Genetics of Development and Discipline of Genetics, School ofMolecular and Biomedical Sciences, The University of Adelaide, Adelaide S.A. 5005, Australia.
Alex Colella
Sonia Dayan
Qingwen Chen
Amanda Choo
Reuben Jacob
Gareth Price
Deon Venter
Robert I Richards
University of Adelaide · AUMater Health Services · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Common chromosomal fragile sites FRA3B and FRA16D are frequent sites of DNA instability in cancer, but their contribution to cancer cell biology is not yet understood. Genes that span these sites (FHIT and WWOX, respectively) are often perturbed (either increased or decreased) in cancer cells and both are able to suppress tumour growth. While WWOX has some tumour suppressor characteristics, its normal role and functional contribution to cancer has not been fully determined. We find that a significant proportion of Drosophila Wwox interactors identified by proteomics and microarray analyses have roles in aerobic metabolism. Functional relationships between Wwox and either CG6439/isocitrate dehydrogenase (Idh) or Cu-Zn superoxide dismutase (Sod) were confirmed by genetic interactions. In addition, altered levels of Wwox resulted in altered levels of endogenous reactive oxygen species. Wwox (like FHIT) contributes to pathways involving aerobic metabolism and oxidative stress, providing an explanation for the 'non-classical tumour suppressor' behaviour of WWOX. Fragile sites, and the genes that span them, are therefore part of a protective response mechanism to oxidative stress and likely contributors to the differences seen in aerobic glycolysis (Warburg effect) in cancer cells.

Indexed as

Chromosome Fragile SitesGenes, Tumor SuppressorAerobiosisAnimalsBase SequenceCell Line, TumorCell RespirationDrosophilaDrosophila ProteinsGene ExpressionGlycolysisHumansIsocitrate DehydrogenaseMass SpectrometryMetabolic Networks and PathwaysMicroarray AnalysisDrosophila ProteinsIsocitrate DehydrogenaseOxidoreductasesReactive Oxygen SpeciesSuperoxide DismutaseTumor Suppressor ProteinsWW Domain-Containing OxidoreductaseWWOX protein, DrosophilaWWOX protein, human

Identifiers

PMID21075834
PMCPMC3016910
OpenAlexW2127295427

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.