Evidence map›Paper›PMID 18452537›Full record

ArticleHistopathology2008

Low levels of WWOX protein immunoexpression correlate with tumour grade and a less favourable outcome in patients with urinary bladder tumours.

D Ramos, M Abba, J A López-Guerrero, J Rubio, E Solsona, S Almenar, A Llombart-Bosch, C M Aldaz

Open access · greenAbstract read
In one paragraph

Article in Histopathology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Loss of fragile WWOX gene leads to senescence escape and genome instability.Cellular and molecular life sciences : CMLS · 2023
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Fragile GeneFrontiers in oncology · 2021
    Article
  10. Frontiers in oncology · 2018
    Review
  11. Correlation of expression of WWOX and JNK with clinicopathologic features in human breast carcinoma.International journal of clinical and experimental pathology · 2018
    Article
  12. Article
  13. WWOX: a fragile tumor suppressor.Experimental biology and medicine (Maywood, N.J.) · 2015
    Review
  14. Regulation of cell signaling and apoptosis by tumor suppressor WWOX.Experimental biology and medicine (Maywood, N.J.) · 2015
    Review
  15. Article
  16. Alternating expression levels ofOncology letters · 2014
    Article
  17. Diverse effect of WWOX overexpression in HT29 and SW480 colon cancer cell lines.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  18. Review
  19. Article
  20. Review
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

8 authors at 3 institutions in 2 countries.

D RamosDepartment of Pathology, School of Medicine, University of Valencia, Valencia, Spain. david.ramos@uv.es
M Abba
J A López-Guerrero
J Rubio
E Solsona
S Almenar
A Llombart-Bosch
C M Aldaz
The University of Texas MD Anderson Cancer Center · USUniversitat de València · ESFundación Instituto Valenciano de Oncología · ES

Funding

Characterization of WWOX, the Cancer Gene Spanning FREA16DR01CA102444 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ALDAZ, C. MARCELO · 2003 to 2014
$3.3M
NCI NIH HHS R01 CA102444
6 · The paper itself

Abstract

aimsTo correlate the immunohistochemical detection of WWOX with histological measures and disease progression within the whole spectrum of urothelial bladder neoplasms. METHODS AND

resultsOne hundred and one patients with primary bladder tumours were retrospectively analysed. Immunohistochemically, a polyclonal antibody was utilized and the level of WWOX protein expression was analysed by using a combined score system based on intensity of the reaction and percentage of immunoreactive tumour cells. WWOX protein expression was consistently expressed in non-neoplastic urothelium, whereas a progressive loss of immunoreactivity was observed as tumour grade and stage increased (P < 0.05). Principal component analysis showed that reduced WWOX immunoexpression was significantly associated with high histological grades (P = 0.001), advanced stage (P = 0.002), tumour size (P = 0.04) and cancer progression (P = 0.028). Invasive urothelial carcinomas of the bladder with squamous metaplasia presented the lowest levels of WWOX protein. Kaplan-Meier analyses demonstrated a significant correlation between loss of WWOX expression and a shorter progression-free survival (P = 0.042), whereas the prediction of overall survival achieved borderline significance (P = 0.053).

conclusionLoss of WWOX immunoexpression strongly correlates with classical clinicopathological factors and appears to be a potential predictive marker of progressive disease.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Transitional CellCell CountFemaleHumansMaleMiddle AgedOxidoreductasesRetrospective StudiesSpainSurvival RateTumor Suppressor ProteinsUrinary Bladder NeoplasmsBiomarkers, TumorOxidoreductasesTumor Suppressor ProteinsWW Domain-Containing OxidoreductaseWWOX protein, human

Identifiers

PMID18452537
PMCPMC4151645
OpenAlexW2020361922

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.