Evidence map›Paper›PMID 30783937›Full record

ArticleMolecular biology reports2019

EGF+61 A>G polymorphism is not associated with lung cancer risk in the Brazilian population.

Ana Carolina Laus, Flavia Escremim de Paula, Marcos Alves de Lima, Carolina Dias Carlos, Izabela Natalia Faria Gomes, Pedro de Marchi, Jenna Kadja Neves Valente, Ana Beatriz Maringolo Pioltini, José Elias Miziara, Carlos Maciel da Silva and 3 more

Abstract read
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In one paragraph

Article in Molecular biology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 3 pooled it
0.5field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 3 syntheses or guidelines pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. 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

13 authors at 1 institution in 2 countries.

Ana Carolina LausMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela St, 1331, Barretos, SP, 14784-400, Brazil.
Flavia Escremim de PaulaMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela St, 1331, Barretos, SP, 14784-400, Brazil.
Marcos Alves de LimaEpidemiology and Biostatistics Department, Barretos Cancer Hospital, Barretos, Brazil.
Carolina Dias CarlosMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela St, 1331, Barretos, SP, 14784-400, Brazil.
Izabela Natalia Faria GomesMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela St, 1331, Barretos, SP, 14784-400, Brazil.
Pedro de MarchiMedical Oncology Department, Barretos Cancer Hospital, Barretos, Brazil.
Jenna Kadja Neves ValenteMedical Oncology Department, Barretos Cancer Hospital, Barretos, Brazil.
Ana Beatriz Maringolo PioltiniMedical Oncology Department, Barretos Cancer Hospital, Barretos, Brazil.
José Elias MiziaraSurgery Department, Barretos Cancer Hospital, Barretos, Brazil.
Carlos Maciel da SilvaSurgery Department, Barretos Cancer Hospital, Barretos, Brazil.
Luciano de Souza VianaMedical Oncology Department, Barretos Cancer Hospital, Barretos, Brazil.
Cristovam Scapulatempo-NetoPathology Department, Barretos Cancer Hospital, Barretos, Brazil.
Rui Manuel ReisMolecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela St, 1331, Barretos, SP, 14784-400, Brazil. ruireis.hcb@gmail.com.ORCID http://orcid.org/0000-0002-9639-7940
Hospital de Câncer de Barretos · BR

Funding

Barretos Cancer Hospital PAIPFinanciadora de Estudos e Projetos 02/2010
6 · The paper itself

Abstract

Epidermal growth factor (EGF) and its receptor (EGFR) play an important role in lung carcinogenesis. A functional single nucleotide polymorphism (SNP) in EGF promoter region (EGF+61 A>G-rs4444903) has been associated with cancer susceptibility. Yet, in lung cancer, the EGF+61 A>G role is unclear. The aim of this study was to evaluate the risk of lung cancer associated with EGF+61 A>G SNP in the Brazilian population. For that, 669 lung cancer patients and 1104 controls were analyzed. EGF+61 A>G genotype was assessed by PCR-RFLP and TaqMan genotyping assay. Both patients and controls were in Hardy-Weinberg equilibrium. As expected, uni- and multivariate analyses showed that tobacco consumption and age were significant risk factors for lung cancer. The genotype frequencies in lung cancer patients were 27.3% of AA, 47.4% of AG and 25.3% of GG, and for controls were 25.3% of AA, 51.6% of AG and 23.1% of GG. The allele frequencies were 51.1% of A and 48.9% of G for both cases and controls. No significant differences for the three genotypes (AA, AG and GG-codominant model) were observed between cases and controls. We then grouped AG and GG (recessive model) genotypes, as well as AA and AG (dominant model), and again, no significant differences were also found. This is the largest study to explore EGF+61 A>G polymorphism association with lung cancer risk and suggests that this SNP is not a risk factor for lung cancer in the Brazilian population.

Indexed as

AdultAgedAged, 80 and overAllelesBrazilCase-Control StudiesEpidermal Growth FactorErbB ReceptorsFemaleGene FrequencyGenetic Predisposition to DiseaseGenetics, PopulationGenotypeHumansLung NeoplasmsMaleEpidermal Growth FactorErbB ReceptorsEGF+61 A>G polymorphismLung cancerRisk factorSNP

Identifiers

PMID30783937
OpenAlexW2916489503

What OpenQuestion holds

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Registered trials

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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.