Evidence map›Paper›PMID 24149047›Full record

ArticleEpigenetics2013

The VHL gene is epigenetically inactivated in pheochromocytomas and abdominal paragangliomas.

Adam Andreasson, Nimrod B Kiss, Stefano Caramuta, Luqman Sulaiman, Fredrika Svahn, Martin Bäckdahl, Anders Höög, C Christofer Juhlin, Catharina Larsson

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  4. TranslatingJCO precision oncology · 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

9 authors at 2 institutions in 1 country.

Adam AndreassonDepartment of Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden.
Nimrod B KissDepartment of Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden.
Stefano CaramutaDepartment of Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden.
Luqman SulaimanDepartment of Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden.
Fredrika SvahnDepartment of Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden.
Martin BäckdahlDepartment of Molecular Medicine and Surgery; Karolinska Institutet; Stockholm, Sweden; Department of Breast and Endocrine Surgery; Karolinska University Hospital; Stockholm, Sweden.
Anders HöögDepartment of Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden; Department of Clinical Pathology and Cytology; Karolinska University Hospital; Stockholm, Sweden.
C Christofer JuhlinDepartment of Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden; Department of Clinical Pathology and Cytology; Karolinska University Hospital; Stockholm, Sweden.
Catharina LarssonDepartment of Oncology-Pathology; Karolinska Institutet; Karolinska University Hospital; Stockholm, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pheochromocytoma (PCC) and abdominal paraganglioma (PGL) are neuroendocrine tumors that present with clinical symptoms related to increased catecholamine levels. About a third of the cases are associated with constitutional mutations in pre-disposing genes, of which some may also be somatically mutated in sporadic cases. However, little is known about inactivating epigenetic events through promoter methylation in these very genes. Using bisulphite pyrosequencing we assessed the methylation density of 11 PCC/PGL disease genes in 96 tumors (83 PCCs and 13 PGLs) and 34 normal adrenal references. Gene expression levels were determined by quantitative RT-PCR. Both tumors and normal adrenal samples exhibited low methylation index (MetI) in the EGLN1 (PDH2), MAX, MEN1, NF1, SDHB, SDHC, SDHD, SDHAF2 (SDH5), and TMEM127 promoters, not exceeding 10% in any of the samples investigated. Aberrant RET promoter methylation was observed in two cases only. For the VHL gene we found increased MetI in tumors as compared with normal adrenals (57% vs. 27%; P<0.001), in malignant vs. benign tumors (63% vs. 55%; P<0.05), and in PGL vs. PCC (66% vs. 55%; P<0.0005). Decreased expression of the VHL gene was observed in all tumors compared with normal adrenals (P<0.001). VHL MetI and gene expressions were inversely correlated (R = -0.359, P<0.0001). Our results show that the VHL gene promoter has increased methylation compared with normal adrenals (MetI>50%) in approximately 75% of PCCs and PGLs investigated, highlighting the role of VHL in the development of these tumors.

Indexed as

Abdominal NeoplasmsAdrenal Gland NeoplasmsBase SequenceCase-Control StudiesDNA MethylationDown-RegulationEpigenesis, GeneticGene Expression Regulation, NeoplasticHumansMolecular Sequence DataParagangliomaPheochromocytomaPromoter Regions, GeneticRNA, MessengerVon Hippel-Lindau Tumor Suppressor ProteinRNA, MessengerVHL protein, humanVon Hippel-Lindau Tumor Suppressor ProteinDNA promoter methylationgene expressionparagangliomaPheochromocytomapyrosequencingqRT-PCRVHL

Identifiers

PMID24149047
PMCPMC3933494
OpenAlexW2074581074

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.