Evidence map›Paper›PMID 24569790›Full record

ArticleNature communications2014

Telomerase reverse transcriptase promoter mutations in primary cutaneous melanoma.

Barbara Heidenreich, Eduardo Nagore, P Sivaramakrishna Rachakonda, Zaida Garcia-Casado, Celia Requena, Victor Traves, Jürgen Becker, Nadem Soufir, Kari Hemminki, Rajiv Kumar

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Nature communications, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed, 1 pooled it
9.7field-weighted citation impact, top 1% 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

93 citing papers in PubMed, 1 synthesis or guideline pooled it, 187 citations in OpenAlex.

  1. Pooled it
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  12. Heliyon · 2023
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33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 5 countries.

Barbara Heidenreich1] Division of Molecular Genetic Epidemiology, German Cancer Research Center, 69120 Heidelberg, Germany [2].
Eduardo Nagore1] Department of Dermatology, Instituto Valenciano de Oncologia, Valencia 46009, Spain [2] Universidad Catolica de Valencia, Valencia 46001, Spain [3].
P Sivaramakrishna RachakondaDivision of Molecular Genetic Epidemiology, German Cancer Research Center, 69120 Heidelberg, Germany.
Zaida Garcia-CasadoLaboratory of Molecular Biology, Instituto Valenciano de Oncologia, Valencia 46009, Spain.
Celia RequenaDepartment of Dermatology, Instituto Valenciano de Oncologia, Valencia 46009, Spain.
Victor TravesDepartment of Pathology, Instituto Valenciano de Oncologia, Valencia 46009, Spain.
Jürgen BeckerDepartment of General Dermatology, Medical University of Graz, Graz 8036, Austria.
Nadem SoufirDepartement de Genetique, Hôpital Bichat-Claude Bernard, APHP, Paris 75877, France.
Kari Hemminki1] Division of Molecular Genetic Epidemiology, German Cancer Research Center, 69120 Heidelberg, Germany [2] Center for Primary Health Care Research, Lund University, Malmö, Lund 221 00, Sweden.
Rajiv KumarDivision of Molecular Genetic Epidemiology, German Cancer Research Center, 69120 Heidelberg, Germany.
Fundación Instituto Valenciano de Oncología · ESHeidelberg University · DEGerman Cancer Research Center · DEHôpital Bichat-Claude-Bernard · FRLund University · SEMedical University of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously reported a disease segregating causal germline mutation in a melanoma family and recurrent somatic mutations in metastasized tumours from unrelated patients in the core promoter region of the telomerase reverse transcriptase (TERT) gene. Here we show that the TERT promoter mutations, besides causing an increased gene expression, associate with increased patient age, increased Breslow thickness and tumour ulceration in 287 primary melanomas. The mutations are more frequent at both intermittently and chronically sun-exposed sites than non-exposed sites and tend to co-occur with BRAF and CDKN2A alterations. The association with parameters generally connected with poor outcome, coupled with high recurrence and mechanistic relevance, raises the possibility of the eventual use of TERT promoter mutations in the disease management.

Indexed as

AdultAgedAged, 80 and overAge FactorsBase SequenceCyclin-Dependent Kinase Inhibitor p16DNA Mutational AnalysisFemaleGene Expression Regulation, NeoplasticGene FrequencyGenotypeHumansMaleMelanomaMiddle AgedMultivariate AnalysisBRAF protein, humanCyclin-Dependent Kinase Inhibitor p16Proto-Oncogene Proteins B-rafTelomerase

Identifiers

PMID24569790
OpenAlexW1989827854

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.