Evidence map›Paper›PMID 26984265›Full record

ArticleBMC cancer2016

GFRA3 promoter methylation may be associated with decreased postoperative survival in gastric cancer.

Lars Lohne Eftang, Jovana Klajic, Vessela N Kristensen, Jörg Tost, Qin Ying Esbensen, Gustav Peter Blom, Ida Rashida Khan Bukholm, Geir Bukholm

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 20% 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, 16 citations in OpenAlex.

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  10. The GDNF Family: A Role in Cancer?Neoplasia (New York, N.Y.) · 2018
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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

8 authors at 4 institutions in 2 countries.

Lars Lohne EftangDepartment of Clinical Molecular Biology and Laboratory Science (EpiGen), Akershus University Hospital, Division of Medicine, Lørenskog, Norway. lars.eftang@medisin.uio.no.ORCID http://orcid.org/0000-0001-8416-4640
Jovana KlajicDepartment of Clinical Molecular Biology and Laboratory Science (EpiGen), Akershus University Hospital, Division of Medicine, Lørenskog, Norway.
Vessela N KristensenDepartment of Clinical Molecular Biology and Laboratory Science (EpiGen), Akershus University Hospital, Division of Medicine, Lørenskog, Norway.
Jörg TostLaboratory for Epigenetics and Environment, Centre National de Génotypage, CEA - Institut de Génomique, Evry, France.
Qin Ying EsbensenDepartment of Clinical Molecular Biology and Laboratory Science (EpiGen), Akershus University Hospital, Division of Medicine, Lørenskog, Norway.
Gustav Peter BlomDepartment of Pathology, Akershus University Hospital, Lørenskog, Norway.
Ida Rashida Khan BukholmInstitute of Clinical Medicine, Akershus University Hospital and University of Oslo, Lørenskog, Norway.
Geir BukholmInfection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.
Akershus University Hospital · NOUniversity of Oslo · NOCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRNorwegian Institute of Public Health · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA large number of epigenetic alterations has been found to be implicated in the etiology of gastric cancer. We have studied the DNA methylation status of 27 500 gene promoter regions in 24 gastric adenocarcinomas from a Norwegian cohort, and aimed at identifying the hypermethylated regions. We have compared our findings to the gene expression in the same tissue, and linked our results to prognosis and survival.

methodsBiopsies from gastric adenocarcinomas and adjacent normal gastric mucosa were obtained from 24 patients following surgical resection of the tumor. Genome-wide DNA methylation profiling of the tumor and matched non-cancerous mucosa was performed. The results were compared to whole transcriptome cDNA microarray analysis of the same material.

resultsMost of the gene promoter regions in both types of tissue showed a low degree of methylation, however there was a small, but significant hypermethylation of the tumors. Hierarchical clustering showed separate grouping of the tumor and normal tissue. Hypermethylation of the promoter region of the GFRA3 gene showed a strong correlation to post-operative survival and several of the clinicopathological parameters, however no difference was found between the two main histological types of gastric cancer. There was only a modest correlation between the DNA methylation status and gene expression.

conclusionsThe different DNA methylation clusters of the tumors and normal tissue indicate that aberrant DNA methylation is a distinct feature of gastric cancer, although there is little difference in the overall, and low, methylation levels between the two tissue types. The GFRA3 promoter region showed marked hypermethylation in almost all tumors, and its correlation with survival and other clinicopathological parameters may have important prognostic significance.

Indexed as

AgedBiomarkers, TumorCpG IslandsDisease-Free SurvivalDNA MethylationFemaleGene Expression Regulation, NeoplasticGlial Cell Line-Derived Neurotrophic Factor ReceptorsHumansLymphatic MetastasisMaleMiddle AgedPostoperative PeriodPrognosisPromoter Regions, GeneticStomach NeoplasmsBiomarkers, TumorGFRA3 protein, humanGlial Cell Line-Derived Neurotrophic Factor ReceptorsDNA methylationGastric cancerGene expressionGFRA3PrognosisSurvival

Identifiers

PMID26984265
PMCPMC4794813
OpenAlexW2300142358

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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.