Evidence map›Paper›PMID 29417620›Full record

ArticleJournal of clinical laboratory analysis2018

HER2 Ile655Val polymorphism is negatively associated with breast cancer susceptibility.

Felipe Campos de Almeida, Bruna Karina Banin Hirata, Carolina Batista Ariza, Roberta Losi Guembarovski, Karen Brajão de Oliveira, Karen Mayumi Suzuki, Alda Losi Guembarovski, Julie Massayo Maeda Oda, Glauco Akelinghton Freire Vitiello, Maria Angelica Ehara Watanabe

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Somatic Mutations inJournal of oncology · 2020
    Review
  6. Article
  7. 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 2 institutions in 1 country.

Felipe Campos de AlmeidaDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0003-0158-1102
Bruna Karina Banin HirataDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0001-6280-0140
Carolina Batista ArizaDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0002-5767-3842
Roberta Losi GuembarovskiDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0002-6291-8621
Karen Brajão de OliveiraDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0001-9666-6963
Karen Mayumi SuzukiDepartment of General Biology, Biological Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0002-1830-5836
Alda Losi GuembarovskiDepartment of Pathology, Clinical and Toxicological Analysis, Health Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0003-0517-3675
Julie Massayo Maeda OdaFederal University of Mato Grosso do Sul, Mato Grosso do Sul, Três Lagoas, Brazil.ORCID http://orcid.org/0000-0002-6166-2169
Glauco Akelinghton Freire VitielloDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0002-3474-8047
Maria Angelica Ehara WatanabeDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Paraná, Brazil.ORCID http://orcid.org/0000-0003-1789-8200
Universidade Estadual de Londrina · BRUniversidade Federal de Mato Grosso do Sul · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPqCoordenadoria de Pós-Graduação, Londrina State University, PROPPG-UELFundação Araucária
6 · The paper itself

Abstract

backgroundThe HER2 (human epidermal growth factor receptor-2) Ile655Val (rs1136201) genetic polymorphism can alter the receptor structure and its auto-activation, which can modify the signal transduction and, consequently, the cell cycle regulation. For this reason, this polymorphism has been extensively investigated as a candidate marker for breast cancer (BC). In this context, the aim of this study was to evaluate the possible influence of HER2 Ile655Val in BC susceptibility and prognostic factors in a Brazilian population.

methodsPolymorphism genotype was assessed through RFLP-PCR in 107 BC patients with clinicopathological data available and in 150 women with no evidence of neoplasia and with no familial history of BC as control group. Association between this polymorphism and BC susceptibility and clinical parameters was evaluated through odds ratio (OR) and chi-squared or Fisher's exact test, respectively.

resultsA significant negative association between valine allele and BC susceptibility in dominant model was found (OR 0.5; 95% CI 0.27-0.93, P = .036). No significant association was found in relation to BC clinicopathological features (tumor size, lymph nodes commitment, histological grade, HER2 overexpression, hormonal receptors, p53, and Ki-67).

conclusionAlthough this polymorphism did not demonstrate potential as a prognostic marker, it may be a suitable susceptibility marker for BC.

Indexed as

breast cancerclinicopathological featuresgenetic polymorphismHER2prognosissingle nucleotide polymorphismsusceptibility

Identifiers

PMID29417620
PMCPMC6817048
OpenAlexW2790201650

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.