Evidence map›Paper›PMID 29507645›Full record

ArticleClinical epigenetics2018

Overexpression of

Alexander Beck, Franziska Trippel, Alexandra Wagner, Saskia Joppien, Max Felle, Christian Vokuhl, Thomas Schwarzmayr, Tim M Strom, Dietrich von Schweinitz, Gernot Längst and 1 more

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

34 citing papers in PubMed, 49 citations in OpenAlex.

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  20. UHRF1 Induces Methylation of theMolecules and cells · 2021
    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

11 authors at 4 institutions in 2 countries.

Alexander Beck *1Department of Pediatric Surgery, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University Munich, Lindwurmstr. 2a, 80337 Munich, Germany.
Franziska Trippel *1Department of Pediatric Surgery, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University Munich, Lindwurmstr. 2a, 80337 Munich, Germany.
Alexandra Wagner1Department of Pediatric Surgery, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University Munich, Lindwurmstr. 2a, 80337 Munich, Germany.
Saskia Joppien1Department of Pediatric Surgery, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University Munich, Lindwurmstr. 2a, 80337 Munich, Germany.
Max Felle2Department of Biochemistry III, University Regensburg, Regensburg, Germany.
Christian Vokuhl3Institute of Paidopathology, Pediatric Tumor Registry, Christian-Albrecht's-University Kiel, Kiel, Germany.
Thomas Schwarzmayr4Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
Tim M Strom4Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
Dietrich von Schweinitz1Department of Pediatric Surgery, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University Munich, Lindwurmstr. 2a, 80337 Munich, Germany.
Gernot Längst2Department of Biochemistry III, University Regensburg, Regensburg, Germany.
Roland Kappler1Department of Pediatric Surgery, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University Munich, Lindwurmstr. 2a, 80337 Munich, Germany.ORCID 0000-0002-8581-2803
Ludwig-Maximilians-Universität München · DEMunich University of Applied Sciences · DEUniversity of Regensburg · DEChristian-Albrechts-Universität zu Kiel · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatoblastoma (HB) is the most common liver tumor of childhood and occurs predominantly within the first 3 years of life. In accordance to its early manifestation, HB has been described to display an extremely low mutation rate. As substitute, epigenetic modifiers seem to play an exceptional role in its tumorigenesis, which holds promise to develop targeted therapies and establish biomarkers for patient risk stratification. Results: We examined the role of a newly described protein complex consisting of three epigenetic regulators, namely E3 ubiquitin-like containing PHD and RING finger domain 1 (UHRF1), ubiquitin-specific-processing protease 7 (USP7), and DNA methyltransferase 1 (DNMT1), in HB. We found the complex to be located on the promoter regions of the pivotal HB-associated tumor suppressor genes (TSGs) Conclusion: These findings suggest that UHRF1 is critical for aberrant TSG silencing and sustained growth signaling in HB and that

Indexed as

Promoter Regions, GeneticUp-RegulationCCAAT-Enhancer-Binding ProteinsCell Line, TumorDNA (Cytosine-5-)-Methyltransferase 1DNA MethylationEpigenesis, GeneticGene Expression Regulation, NeoplasticHepatoblastomaHumansLiver NeoplasmsPrognosisSurvival AnalysisTumor Suppressor ProteinsUbiquitin-Protein LigasesUbiquitin-Specific Peptidase 7CCAAT-Enhancer-Binding ProteinsDNA (Cytosine-5-)-Methyltransferase 1DNMT1 protein, humanTumor Suppressor ProteinsUbiquitin-Protein LigasesUbiquitin-Specific Peptidase 7UHRF1 protein, humanUSP7 protein, humanBiomarkerDNA methylationDNMT1Epigenetic silencingHepatoblastomaHistone methylationTumor suppressor genesUHRF1USP7

Identifiers

PMID29507645
PMCPMC5833129
OpenAlexW2794608908

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.