Evidence map›Paper›PMID 27449293›Full record

ArticleOncotarget2016

TERT promoter mutations in melanoma render TERT expression dependent on MAPK pathway activation.

Andrelou F Vallarelli, P Sivaramakrishna Rachakonda, Jocelyne André, Barbara Heidenreich, Laurence Riffaud, Armand Bensussan, Rajiv Kumar, Nicolas Dumaz

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Role ofMolecular and clinical oncology · 2025
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  18. Mechanisms of TERT Reactivation and Its Interaction with BRAFV600E.Endocrinology and metabolism (Seoul, Korea) · 2020
    Review
  19. Review
  20. 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

8 authors at 4 institutions in 3 countries.

Andrelou F VallarelliINSERM, U976, Skin Research Centre, Hôpital Saint-Louis, Paris, F-75010, France.
P Sivaramakrishna RachakondaDivision of Molecular Genetic Epidemiology, German Cancer Research Center, 69120 Heidelberg, Germany.
Jocelyne AndréINSERM, U976, Skin Research Centre, Hôpital Saint-Louis, Paris, F-75010, France.
Barbara HeidenreichDivision of Molecular Genetic Epidemiology, German Cancer Research Center, 69120 Heidelberg, Germany.
Laurence RiffaudINSERM, U976, Skin Research Centre, Hôpital Saint-Louis, Paris, F-75010, France.
Armand BensussanINSERM, U976, Skin Research Centre, Hôpital Saint-Louis, Paris, F-75010, France.
Rajiv KumarDivision of Molecular Genetic Epidemiology, German Cancer Research Center, 69120 Heidelberg, Germany.
Nicolas DumazINSERM, U976, Skin Research Centre, Hôpital Saint-Louis, Paris, F-75010, France.
Délégation Paris 7 · FRHeidelberg University · DEGerman Cancer Research Center · DESorbonne Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanism of telomerase re-activation in cancer had remained elusive until the discovery of frequent mutations in the promoter of the TERT gene that encodes the catalytic reverse transcriptase subunit of telomerase. We investigated the regulation of TERT expression in melanoma cell lines and our results show that promoter mutations render TERT expression dependent on MAPK activation due to oncogenic BRAF or NRAS mutations. Mutations in the TERT promoter create binding sites for ETS transcription factors. ETS1, expressed in melanoma cell lines, undergoes activating phosphorylation by ERK at Thr38 residue as a consequence of constitutively activated MAPK pathway. We demonstrate that ETS1 binds on the mutated TERT promoter leading to the re-expression of the gene. The inhibition of ETS1 resulted in reduced TERT expression. We provide evidence that the TERT promoter mutations provide a direct link between TERT expression and MAPK pathway activation due to BRAF or NRAS mutations via the transcription factor ETS1.

Indexed as

Gene Expression Regulation, NeoplasticMutationCell Line, TumorGTP PhosphohydrolasesHumansMAP Kinase Signaling SystemMelanomaMembrane ProteinsPromoter Regions, GeneticProto-Oncogene Protein c-ets-1Proto-Oncogene Proteins B-rafRNA InterferenceTelomeraseBRAF protein, humanGTP PhosphohydrolasesMembrane ProteinsNRAS protein, humanProto-Oncogene Protein c-ets-1Proto-Oncogene Proteins B-rafTelomeraseBRAFETS1MAPK pathwaymelanomatelomerase

Identifiers

PMID27449293
PMCPMC5288173
OpenAlexW2466234008

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.