Evidence map›Paper›PMID 26545983›Full record

ArticleBMC medical genomics2015

DNA methylation subgroups in melanoma are associated with proliferative and immunological processes.

Martin Lauss, Markus Ringnér, Anna Karlsson, Katja Harbst, Christian Busch, Jürgen Geisler, Per Eystein Lønning, Johan Staaf, Göran Jönsson

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  13. CpG Island Methylator Phenotype-A Hope for the Future or a Road to Nowhere?International journal of molecular sciences · 2022
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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

9 authors at 2 institutions in 2 countries.

Martin LaussDepartment of Oncology and Pathology, Clinical Sciences, Lund University Hospital, Lund University, Lund, 221 85, Sweden. martin.lauss@med.lu.se.
Markus RingnérDepartment of Oncology and Pathology, Clinical Sciences, Lund University Hospital, Lund University, Lund, 221 85, Sweden. markus.ringner@med.lu.se.
Anna KarlssonDepartment of Oncology and Pathology, Clinical Sciences, Lund University Hospital, Lund University, Lund, 221 85, Sweden. anna_f.karlsson@med.lu.se.
Katja HarbstDepartment of Oncology and Pathology, Clinical Sciences, Lund University Hospital, Lund University, Lund, 221 85, Sweden. katja.harbst@med.lu.se.
Christian BuschSection of Oncology, Department of Clinical Science, University of Bergen, Bergen, Norway. busch.christian@gmail.com.
Jürgen GeislerSection of Oncology, Department of Clinical Science, University of Bergen, Bergen, Norway. juergen.geisler@medisin.uio.no.
Per Eystein LønningSection of Oncology, Department of Clinical Science, University of Bergen, Bergen, Norway. per.eystein.lonning@helse-bergen.no.
Johan StaafDepartment of Oncology and Pathology, Clinical Sciences, Lund University Hospital, Lund University, Lund, 221 85, Sweden. johan.staaf@med.lu.se.
Göran JönssonDepartment of Oncology and Pathology, Clinical Sciences, Lund University Hospital, Lund University, Lund, 221 85, Sweden. goran_b.jonsson@med.lu.se.
Lund University · SEUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDNA methylation at CpG dinucleotides is modified in tumorigenesis with potential impact on transcriptional activity.

methodsWe used the Illumina 450 K platform to evaluate DNA methylation patterns of 50 metastatic melanoma tumors, with matched gene expression data.

resultsWe identified three different methylation groups and validated the groups in independent data from The Cancer Genome Atlas. One group displayed hypermethylation of a developmental promoter set, genome-wide demethylation, increased proliferation and activity of the SWI/SNF complex. A second group had a methylation pattern resembling stromal and leukocyte cells, over-expressed an immune signature and had improved survival rates in metastatic tumors (p < 0.05). A third group had intermediate methylation levels and expressed both proliferative and immune signatures. The methylation groups corresponded to some degree with previously identified gene expression phenotypes.

conclusionsMelanoma consists of divergent methylation groups that are distinguished by promoter methylation, proliferation and content of immunological cells.

Indexed as

DNA MethylationGene Expression ProfilingCell ProliferationCpG IslandsFemaleGenomicsHumansMaleMelanomaNeoplasm MetastasisPromoter Regions, Genetic

Identifiers

PMID26545983
PMCPMC4636848
OpenAlexW2157681026

What OpenQuestion holds

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LicenceCC BY
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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.