Evidence map›Paper›PMID 11438452›Full record

ArticleThe American journal of pathology2001

Reduced expression of plakoglobin correlates with adverse outcome in patients with neuroblastoma.

R Amitay, D Nass, D Meitar, I Goldberg, B Davidson, L Trakhtenbrot, F Brok-Simoni, A Ben-Ze'ev, G Rechavi, Y Kaufmann

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Expression and epigenetic modulation of sonic hedgehog-GLI1 pathway genes in neuroblastoma cell lines and tumors.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2011
    Article
  3. Article
  4. Article
  5. Article
  6. Plakoglobin suppresses keratinocyte motility through both cell-cell adhesion-dependent and -independent mechanisms.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  7. Phenotypic conversion of human mammary carcinoma cells by autocrine human growth hormone.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  8. Review
  9. 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

10 authors at 5 institutions in 4 countries.

R AmitayInstitute of Hematology, the Department of Pathology, and the Institute of Pediatric Oncology, Chaim Sheba Medical Center, Tel-Hashomer. Weizmann Institute of Science, Rehovot, Israel.
D Nass
D Meitar
I Goldberg
B Davidson
L Trakhtenbrot
F Brok-Simoni
A Ben-Ze'ev
G Rechavi
Y Kaufmann
Tel Aviv University · ILSheba Medical Center · ILNorwegian Cancer Society · NOPediatric Oncology Group · CAWeizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plakoglobin and its homologue beta-catenin are cytoplasmic proteins that mediate adhesive functions by interacting with cadherin receptors and signaling activities by interacting with transcription factors. It has been suggested that plakoglobin can suppress tumorigenicity whereas beta-catenin can act as an oncogene. We investigated the correlation between the expression pattern of N-cadherin, beta-catenin, and plakoglobin and tumor behavior in primary tumors of 20 neuroblastoma patients of all stages and in 11 human neuroblastoma cell lines. N-cadherin and beta-catenin were detected in 9 of 11 and 11 of 11 cell lines, respectively, whereas plakoglobin was undetectable or severely reduced in 6 of 11 cell lines. Tumor cells from 16 of 20 patients expressed N-cadherin and 20 of 20 patients expressed beta-catenin at levels similar to those of normal ganglion cells. Plakoglobin was undetectable in 9 of 20 tumors. Plakoglobin deficiency in the primary tumors was significantly associated with adverse clinical outcome. Five of the patients with plakoglobin-negative tumors died whereas four patients are alive without evident disease. In contrast, all patients with plakoglobin-positive tumors are alive; 2 of 11 are alive with the disease and 9 of 11 are alive without evident disease. These results suggest that down-regulation of plakoglobin may be of prognostic value for neuroblastoma patients as predictor of poor outcome.

Indexed as

Trans-Activatorsbeta CateninBlotting, WesternCadherinsChildChild, PreschoolCytoskeletal ProteinsDesmoplakinsgamma CateninHumansImmunohistochemistryInfantInfant, NewbornNeoplasm StagingNeuroblastomaSurvival Analysisbeta CateninCadherinsCTNNB1 protein, humanCytoskeletal ProteinsDesmoplakinsgamma CateninTrans-Activators

Identifiers

PMID11438452
PMCPMC1850431
OpenAlexW2016054080

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.