Evidence map›Paper›PMID 16416221›Full record

ArticleDigestive diseases and sciences2006

TP53 gene mutations are rare in nondysplastic Barrett's esophagus.

Kamila Novotna, Marie Trkova, Alexandr Pazdro, Milan Smejkal, Alzbeta Soukupova, Daniela Kodetova, Premysl Smejkal, Zdenek Sedlacek

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Digestive diseases and sciences, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Her-2 Expression in Gastroesophageal Intestinal Metaplasia, Dysplasia, and Adenocarcinoma.Applied immunohistochemistry & molecular morphology : AIMM · 2016
    Article
  5. Risk factors associated with Barrett's epithelial dysplasia.World journal of gastroenterology · 2014
    Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Kamila NovotnaInstitute of Biology and Medical Genetics, Charles University Second Medical School, 15006, Prague 5, Czech Republic. kamila.novotna@lfmotol.cuni.cz
Marie Trkova
Alexandr Pazdro
Milan Smejkal
Alzbeta Soukupova
Daniela Kodetova
Premysl Smejkal
Zdenek Sedlacek
Charles University · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In search of potential prognostic markers, we analyzed a large series of tissues of Barrett's esophagus and samples of adenocarcinomas arising in the terrain of Barrett's esophagus for TP53 gene mutations by direct sequencing of exons 5 to 9 of the TP53 gene. While 9 of 21 adenocarcinomas tested (42.9%) contained a TP53 mutation, none of 24 samples from Barrett's esophagus were mutated. This observation suggests that TP53 gene mutation may be a relatively late event in the progression from nondysplastic Barrett's esophagus to adenocarcinoma of esophagus. Therefore, TP53 gene mutations alone are not likely to represent a widely useful prognostic marker of the risk of progression to malignancy, at least not in Barrett's esophagus without dysplasia.

Indexed as

MutationAdenocarcinomaAdultAgedAged, 80 and overBarrett EsophagusBiopsyDisease ProgressionDNAEsophageal NeoplasmsExonsFemaleGenes, p53Genetic MarkersHumansMaleDNAGenetic Markers

Identifiers

PMID16416221
OpenAlexW1981182893

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.