Evidence map›Paper›PMID 24594201›Full record

ArticleGenetics research2014

Spectrum of somatic EGFR, KRAS, BRAF, PTEN mutations and TTF-1 expression in Brazilian lung cancer patients.

Juliana G Carneiro, Patricia G Couto, Luciana Bastos-Rodrigues, Maria Aparecida C Bicalho, Paula V Vidigal, Alyne Vilhena, Nilson F Amaral, Allen E Bale, Eitan Friedman, Luiz De Marco

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Genetics research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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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 4 institutions in 3 countries.

Juliana G CarneiroFaculdade de Ciências Médicas, Centro de Ensino Superior e Desenvolvimento, Campina Grande, 58411-020, Brasil.
Patricia G CoutoDepartment of Surgery, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Brasil.
Luciana Bastos-RodriguesDepartment of Surgery, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Brasil.
Maria Aparecida C BicalhoDepartment of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Brasil.
Paula V VidigalDepartment of Pathology, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Brasil.
Alyne VilhenaHospital Julia Kubitscheck, Belo Horizonte, 30620-470, Brasil.
Nilson F AmaralHospital Julia Kubitscheck, Belo Horizonte, 30620-470, Brasil.
Allen E BaleDepartment of Genetics, Yale University School of Medicine, New Haven, CT 06520-8005, USA.
Eitan FriedmanThe Susanne Levy Gertner Oncogenetics Unit, Chaim Sheba Medical Center, Tel-Hashomer, 52621, Israel.
Luiz De MarcoDepartment of Surgery, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Brasil.
Universidade Federal de Minas Gerais · BRFundação Hospitalar do Estado de Minas Gerais · BRSheba Medical Center · ILYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the leading global cause of cancer-related mortality. Inter-individual variability in treatment response and prognosis has been associated with genetic polymorphisms in specific genes: EGFR, KRAS, BRAF, PTEN and TTF-1. Somatic mutations in EGFR and KRAS genes are reported at rates of 15-40% in non-small cell lung cancer (NSCLC) in ethnically diverse populations. BRAF and PTEN are commonly mutated genes in various cancer types, including NSCLC, with PTEN mutations exerting an effect on the therapeutic response of EGFR/AKT/PI3K pathway inhibitors. TTF-1 is expressed in approximately 80% of lung adenocarcinomas and its positivity correlates with higher prevalence of EGFR mutation in this cancer type. To determine molecular markers for lung cancer in Brazilian patients, the rate of the predominant EGFR, KRAS, BRAF and PTEN mutations, as well as TTF-1 expression, was assessed in 88 Brazilian NSCLC patients. EGFR exon 19 deletions (del746-750) were detected in 3/88 (3·4%) patients. Activating KRAS mutations in codons 12 and 61 were noted in five (5·7%) and two (2·3%) patients, respectively. None of the common somatic mutations were detected in either the BRAF or PTEN genes. TTF-1 was overexpressed in 40·7% of squamous-cell carcinoma (SCC). Our findings add to a growing body of data that highlights the genetic heterogeneity of the abnormal EGFR pathway in lung cancer among ethnically diverse populations.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overBrazilCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellCase-Control StudiesDNA-Binding ProteinsErbB ReceptorsFemaleGenetic Predisposition to DiseaseHumansImmunoenzyme TechniquesLung NeoplasmsMaleBRAF protein, humanDNA-Binding ProteinsEGFR protein, humanErbB ReceptorsKRAS protein, humanProto-Oncogene ProteinsProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)PTEN PhosphohydrolasePTEN protein, humanras ProteinsTranscription FactorsTTF1 protein, human

Identifiers

PMID24594201
PMCPMC7045132
OpenAlexW2147568566

What OpenQuestion holds

Textmetadata
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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.