Evidence map›Paper›PMID 28514750›Full record

ArticleOncotarget2017

Epigenome-wide association study in hepatocellular carcinoma: Identification of stochastic epigenetic mutations through an innovative statistical approach.

Davide Gentilini, Stefania Scala, Germano Gaudenzi, Paolo Garagnani, Miriam Capri, Matteo Cescon, Gian Luca Grazi, Maria Giulia Bacalini, Serena Pisoni, Alessandra Dicitore and 7 more

Abstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

44 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  12. A novel BRAF::PTPRN2 fusion in meningioma: a case report.Acta neuropathologica communications · 2023
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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

17 authors.

Davide GentiliniIstituto Auxologico Italiano IRCCS, Cusano Milanino, Milan, Italy.
Stefania ScalaFunctional Genomics, Istituto Nazionale per lo Studio e la Cura dei Tumori, IRCCS Fondazione "G. Pascale", Napoli, Italy.
Germano GaudenziDepartment of Clinical Sciences and Community Health (DISCCO), University of Milan, Milan, Italy.
Paolo GaragnaniDepartment of Experimental, Diagnostic and Specialty Medicine, Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Miriam CapriDepartment of Experimental, Diagnostic and Specialty Medicine, Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Matteo CesconDIMEC-Department of General Surgery and Medicine Sciences, S. Orsola-Malpighi Hospital, Bologna, Italy.
Gian Luca GraziRegina Elena National Cancer Institute Via Elio Chianesi 53, Rome, Italy.
Maria Giulia BacaliniIRCCS Institute of Neurological Sciences, Bologna, Italy.
Serena PisoniIstituto Auxologico Italiano IRCCS, Cusano Milanino, Milan, Italy.
Alessandra DicitoreIstituto Auxologico Italiano IRCCS, Cusano Milanino, Milan, Italy.
Luisa CircelliDepartment of Experimental Oncology, Laboratory of Molecular Biology and Viral Oncology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Fondazione "G. Pascale", Napoli, Italy.
Sara SantagataFunctional Genomics, Istituto Nazionale per lo Studio e la Cura dei Tumori, IRCCS Fondazione "G. Pascale", Napoli, Italy.
Francesco IzzoDepartment of Surgical Oncology, Abdominal and Hepatobiliary Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori, IRCCS Fondazione " G. Pascale", Napoli, Italy.
Anna Maria Di BlasioIstituto Auxologico Italiano IRCCS, Cusano Milanino, Milan, Italy.
Luca PersaniIstituto Auxologico Italiano IRCCS, Cusano Milanino, Milan, Italy.
Claudio FranceschiDepartment of Experimental, Diagnostic and Specialty Medicine, Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Giovanni VitaleIstituto Auxologico Italiano IRCCS, Cusano Milanino, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) results from accumulation of both genetic and epigenetic alterations. We investigated the genome-wide DNA methylation profile in 69 pairs of HCC and adjacent non-cancerous liver tissues using the Infinium HumanMethylation 450K BeadChip array. An innovative analytical approach has been adopted to identify Stochastic Epigenetic Mutations (SEMs) in HCC.HCC and peritumoral tissues showed a different epigenetic profile, mainly characterized by loss of DNA methylation in HCC. Total number of SEMs was significantly higher in HCC tumor (median: 77,370) than in peritumoral (median: 5,656) tissues and correlated with tumor grade. A significant positive association emerged between SEMs measured in peritumoral tissue and hepatitis B and/or C virus infection status. A restricted number of SEMs resulted to be shared by more than 90% of HCC tumor samples and never present in peritumoral tissue. This analysis allowed the identification of four epigenetically regulated candidate genes (AJAP1, ADARB2, PTPRN2, SDK1), potentially involved in the pathogenesis of HCC.In conclusion, HCC showed a methylation profile completely deregulated and very far from adjacent non-cancerous liver tissues. The SEM analysis provided valuable clues for further investigations in understanding the process of tumorigenesis in HCC.

Indexed as

Epigenesis, GeneticEpigenomicsGenome-Wide Association StudyAdultAgedBiomarkers, TumorCarcinogenesisCarcinoma, HepatocellularCluster AnalysisComputational BiologyDNA MethylationFemaleGene Expression ProfilingGenetic Predisposition to DiseaseHumansLiver NeoplasmsBiomarkers, TumorDNA methylationepigeneticsgenome-widehepatocellular carcinomastochastic epigenetic mutation

Identifiers

PMID28514750
PMCPMC5522036

What OpenQuestion holds

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Registered trials

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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.