Evidence map›Paper›PMID 27192129›Full record

ArticleGenetics and molecular biology2016

CDH1 mutations in gastric cancer patients from northern Brazil identified by Next- Generation Sequencing (NGS).

Antonette El-Husny, Milene Raiol-Moraes, Marcos Amador, André M Ribeiro-Dos-Santos, André Montagnini, Silvanira Barbosa, Artur Silva, Paulo Assumpção, Geraldo Ishak, Sidney Santos and 3 more

Open access · goldAbstract read
In one paragraph

Article in Genetics and molecular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Genes · 2022
    Article
  7. How does genetic testing influence anxiety, depression, and quality of life? A hereditary breast and ovarian cancer syndrome suspects trial.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2021
    Article
  8. Review
  9. piRNAs in Gastric Cancer: A New Approach Towards Translational Research.International journal of molecular sciences · 2020
    Review
  10. Frequency of CDH1 germline variants and contribution of dietary habits in early age onset gastric cancer patients in Brazil.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2019
    Article
  11. Review
  12. 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

13 authors at 2 institutions in 1 country.

Antonette El-HusnyLaboratório de Genética Humana e Médica (LGHM), Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Milene Raiol-MoraesLaboratório de Genética Humana e Médica (LGHM), Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Marcos AmadorLaboratório de Genética Humana e Médica (LGHM), Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
André M Ribeiro-Dos-SantosLaboratório de Genética Humana e Médica (LGHM), Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
André MontagniniInstituto Sírio-Libanês de Ensino e Pesquisa, Hospital Sírio-Libanês, São Paulo, SP, Brazil.
Silvanira BarbosaLaboratório de Polimorfismo de DNA - Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Artur SilvaRede de Pesquisa em Genômica Populacional Humana, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Paulo AssumpçãoRede de Pesquisa em Genômica Populacional Humana, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Geraldo IshakRede de Pesquisa em Genômica Populacional Humana, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Sidney SantosLaboratório de Genética Humana e Médica (LGHM), Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Pablo PintoLaboratório de Genética Humana e Médica (LGHM), Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Aline CruzLaboratório de Genética Humana e Médica (LGHM), Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Ândrea Ribeiro-Dos-SantosLaboratório de Genética Humana e Médica (LGHM), Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, PA, Brazil.
Universidade Federal do Pará · BRHospital Sírio-Libanês · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer is considered to be the fifth highest incident tumor worldwide and the third leading cause of cancer deaths. Developing regions report a higher number of sporadic cases, but there are only a few local studies related to hereditary cases of gastric cancer in Brazil to confirm this fact. CDH1 germline mutations have been described both in familial and sporadic cases, but there is only one recent molecular description of individuals from Brazil. In this study we performed Next Generation Sequencing (NGS) to assess CDH1 germline mutations in individuals who match the clinical criteria for Hereditary Diffuse Gastric Cancer (HDGC), or who exhibit very early diagnosis of gastric cancer. Among five probands we detected CDH1 germline mutations in two cases (40%). The mutation c.1023T > G was found in a HDGC family and the mutation c.1849G > A, which is nearly exclusive to African populations, was found in an early-onset case of gastric adenocarcinoma. The mutations described highlight the existence of gastric cancer cases caused by CDH1 germline mutations in northern Brazil, although such information is frequently ignored due to the existence of a large number of environmental factors locally. Our report represent the first CDH1 mutations in HDGC described from Brazil by an NGS platform.

Identifiers

PMID27192129
PMCPMC4910547
OpenAlexW2373509286

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.