Evidence map›Paper›PMID 33512806›Full record

ArticleClinical and translational gastroenterology2020

Investigation on the Role of PALB2 Gene in CDH1-Negative Patients With Hereditary Diffuse Gastric Cancer.

Marta Carreño, Laura Pena-Couso, Fátima Mercadillo, José Perea, Miguel Urioste

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Hereditary Diffuse Gastric Cancer: A 2022 Update.Journal of personalized medicine · 2022
    Review
  2. 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

5 authors at 2 institutions in 1 country.

Marta CarreñoFamilial Cancer Clinical Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Laura Pena-CousoFamilial Cancer Clinical Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Fátima MercadilloFamilial Cancer Clinical Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
José PereaSurgery Department, Fundación Jiménez Díaz University Hospital, Madrid, Spain.
Miguel UriosteFamilial Cancer Clinical Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Spanish National Cancer Research Centre · ESHospital Universitario Fundación Jiménez Díaz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNot all patients with hereditary diffuse gastric cancer (HDGC) are found to carry germline pathogenic variants in the associated gene CDH1, which translates into a challenging clinical management and poor cancer prevention. Thus, several studies have searched for other candidate genes, among which stands PALB2. Our work explores the implication of this known cancer gene in HDGC.

methodsWe searched for germline PALB2 variants by Sanger sequencing in a series of 58 patients with HDGC who tested negative for CDH1 alterations.

resultsNo clearly pathogenic variants in PALB2 were found in these patients. Only 5 rare genetic variants were identified, 3 of which were classified as variants of uncertain significance. DISCUSSION: Despite the promising association between PALB2 and HDGC suggested by certain works in the literature, our findings do not support PALB2 as a high predisposition gene for HDGC. Larger studies are needed to define its role in this disease and therefore improve cancer prevention.

Indexed as

AdultAgedAntigens, CDCadherinsFanconi Anemia Complementation Group N ProteinFemaleGenetic CounselingGenetic Predisposition to DiseaseGerm-Line MutationHumansMaleMiddle AgedNeoplastic Syndromes, HereditaryPedigreeStomach NeoplasmsYoung AdultAntigens, CDCadherinsCDH1 protein, humanFanconi Anemia Complementation Group N ProteinPALB2 protein, human

Identifiers

PMID33512806
PMCPMC7721210
OpenAlexW3112701783

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.