Evidence map›Paper›PMID 15122326›Full record

ArticleOncogene2004

E2F3 amplification and overexpression is associated with invasive tumor growth and rapid tumor cell proliferation in urinary bladder cancer.

Martin Oeggerli, Sanja Tomovska, Peter Schraml, Daniele Calvano-Forte, Salome Schafroth, Ronald Simon, Thomas Gasser, Michael J Mihatsch, Guido Sauter

Abstract read
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In one paragraph

Article in Oncogene, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
10.8field-weighted citation impact, top 1% 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

69 citing papers in PubMed, 160 citations in OpenAlex.

  1. Article
  2. Review
  3. Machine Learning for Detecting and Analyzing Chromoanagenesis Events.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
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  9. The multifaceted roles of cohesin in cancer.Journal of experimental & clinical cancer research : CR · 2022
    Review
  10. Article
  11. Article
  12. Knockdown of E2F4 suppresses the growth of ovarian cancer cells through the cell cycle pathway.International journal of clinical and experimental pathology · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. MiR-22 suppresses the growth and metastasis of bladder cancer cells by targeting E2F3.International journal of clinical and experimental pathology · 2020
    Article
  18. Hypoxia in the Initiation and Progression of Neuroblastoma Tumours.International journal of molecular sciences · 2019
    Review
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Martin OeggerliInstitute of Pathology, Schoenbeinstrasse 40, CH-4031 Basel, Switzerland.
Sanja Tomovska
Peter Schraml
Daniele Calvano-Forte
Salome Schafroth
Ronald Simon
Thomas Gasser
Michael J Mihatsch
Guido Sauter
Psychiatry Baselland · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

E2F3 is located in the 6p22 bladder amplicon and encodes a transcription factor important for cell cycle regulation and DNA replication. To further investigate the role of E2F3 in bladder cancer, a tissue microarray containing samples from 2317 bladder tumors was used for gene copy number and expression analysis by means of fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC). E2F3 amplification was strongly associated with invasive tumor phenotype and high tumor grade (P < 0.0001 each). None of 272 pTaG1/G2 tumors, but 35 of 311 pT1-4 carcinomas (11.3%), had E2F3 amplification. A high E2F3 expression level was associated with high grade, advanced stage, and E2F3 gene amplification (P < 0.0001 each). To evaluate whether E2F3 expression correlates with tumor proliferation, the Ki67 labeling index (LI) was analysed for each tumor. There was a strong association between a high Ki67 LI and E2F3 expression (P < 0.0001), which was independent of grade and stage. We conclude that E2F3 is frequently amplified and overexpressed in invasively growing bladder cancer (stage pT1-4). E2F3 expression appears to provide a growth advantage to tumor cells by activating cell proliferation in a subset of bladder tumors.

Indexed as

Gene AmplificationCell DivisionE2F3 Transcription FactorHumansImmunohistochemistryIn Situ Hybridization, FluorescenceKi-67 AntigenPrognosisProtein Array AnalysisTranscription FactorsUrinary Bladder NeoplasmsE2F3 protein, humanE2F3 Transcription FactorKi-67 AntigenTranscription Factors

Identifiers

PMID15122326
OpenAlexW2086642593

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.