Evidence map›Paper›PMID 17309796›Full record

ArticleWorld journal of surgical oncology2007

Aberrant nuclear localization of beta-catenin without genetic alterations in beta-catenin or Axin genes in esophageal cancer.

Junjo Kudo, Tadashi Nishiwaki, Nobuhiro Haruki, Hideyuki Ishiguro, Yasuyuki Shibata, Yukio Terashita, Hironori Sugiura, Noriyuki Shinoda, Masahiro Kimura, Yoshiyuki Kuwabara and 1 more

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
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  4. Targeting cancer stem cell pathways for cancer therapy.Signal transduction and targeted therapy · 2020
    Review
  5. The Expression of Tripartite Motif Protein 36 andGastroenterology research and practice · 2020
    Article
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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

11 authors at 1 institution in 1 country.

Junjo KudoDepartment of Surgery II, Nagoya City University Medical School, Nagoya, Japan. dr_kudo@yahoo.co.jp
Tadashi Nishiwaki
Nobuhiro Haruki
Hideyuki Ishiguro
Yasuyuki Shibata
Yukio Terashita
Hironori Sugiura
Noriyuki Shinoda
Masahiro Kimura
Yoshiyuki Kuwabara
Yoshitaka Fujii
Nagoya City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundbeta-catenin is a multifunctional protein involved in two apparently independent processes: cell-cell adhesion and signal transduction. beta-catenin is involved in Wnt signaling pathway that regulates cellular differentiation and proliferation. In this study, we investigated the expression pattern of beta-catenin and cyclin D1 using immunohistochemistry and searched for mutations in exon 3 of the beta-catenin gene and Axin gene in esophageal squamous cell carcinoma. MATERIALS AND

methodsSamples were obtained from 50 esophageal cancer patients. Immunohistochemical staining for beta-catenin and cyclin D1 was done. Mutational analyses of the exon3 of the beta-catenin gene and Axin gene were performed on tumors with nuclear beta-catenin expression.

resultsFour (8%) esophageal cancer tissues showed high nuclear beta-catenin staining. Overexpression of cyclin D1 was observed in 27 out of 50 (54%) patients. All four cases that showed nuclear beta-catenin staining overexpressed cyclin D1. No relationship was observed between the expression pattern of beta-catenin and cyclin D1 and age, sex, tumor size, stage, differentiation grade, lymph node metastasis, response to chemotherapy, or survival. No mutational change was found in beta-catenin exon 3 in the four cases with nuclear beta-catenin staining. Sequencing analysis of the Axin cDNA revealed only a splicing variant (108 bp deletion, position 2302-2409) which was present in the paired normal mucosa.

conclusionA fraction of esophageal squamous cell carcinomas have abnormal nuclear accumulation of beta-catenin accompanied with increased cyclin D1 expression. Mutations in beta-catenin or axin genes are not responsible for this abnormal localization of beta-catenin.

Indexed as

AgedAxin Proteinbeta CateninBiopsy, NeedleCarcinoma, Squamous CellCase-Control StudiesDNA Mutational AnalysisDNA, NeoplasmEsophageal NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryMaleMiddle AgedNeoplasm StagingAxin Proteinbeta CateninDNA, NeoplasmNuclear Localization SignalsRepressor ProteinsWnt Proteins

Identifiers

PMID17309796
PMCPMC1808060
OpenAlexW1945980268

What OpenQuestion holds

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LicenceCC BY
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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.