Evidence map›Paper›PMID 31053176›Full record

ArticleClinical epigenetics2019

DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer.

Christoph Weigel, Jittiporn Chaisaingmongkol, Yassen Assenov, Christine Kuhmann, Volker Winkler, Irene Santi, Olga Bogatyrova, Simone Kaucher, Justo L Bermejo, Suet Y Leung and 19 more

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  16. Epigenetic Signaling and RNA Regulation in Cardiovascular Diseases.International journal of molecular sciences · 2020
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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

29 authors at 11 institutions in 5 countries.

Christoph WeigelDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Jittiporn ChaisaingmongkolChulabhorn Research Institute, Bangkok, Thailand.
Yassen AssenovDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Christine KuhmannDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Volker WinklerInstitute of Public Health, University of Heidelberg, Heidelberg, Germany.
Irene SantiInstitute of Public Health, University of Heidelberg, Heidelberg, Germany.
Olga BogatyrovaDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Simone KaucherInstitute of Public Health, University of Heidelberg, Heidelberg, Germany.
Justo L BermejoInstitute of Medical Biometry and Informatics, University Hospital Heidelberg, Heidelberg, Germany.
Suet Y LeungDepartment of Pathology, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong, China.
Tsun L ChanDepartment of Pathology, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong, China.
Felix LasitschkaInstitute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Manfred H BohrerMedical Hospital, Institute of Pathology, Ludwigshafen, Germany.
Alexander MarxInstitute of Pathology, University Medical Centre Mannheim, Mannheim, Germany.
Roland Heyny-von HaußenCenter of Pathology, Klinikum Darmstadt, Darmstadt, Germany.
Christel Herold-MendeDepartment of Otorhinolaryngology, Head and Neck Surgery, University of Heidelberg, Heidelberg, Germany.
Gerhard DyckhoffDepartment of Otorhinolaryngology, Head and Neck Surgery, University of Heidelberg, Heidelberg, Germany.
Petra BoukampDivision of Genetics of Skin Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Klaus W DelankMedical Hospital, Head and Neck Surgery, Ludwigshafen, Germany.
Karl HörmannDepartment of Otorhinolaryngology, Head and Neck Surgery, University Hospital of Mannheim, Mannheim, Germany.
Burkhard M LippertDepartment of Otorhinolaryngology, Head and Neck Surgery, Heilbronn, Germany.
Gerald BaierDepartment of Otorhinolaryngology, Head and Neck Surgery, Academic Teaching Hospital, Darmstadt, Germany.
Andreas DietzDepartment of Otorhinolaryngology, Head and Neck Surgery, University of Leipzig, Leipzig, Germany.
Christopher C OakesDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Christoph PlassDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Heiko BecherInstitute of Public Health, University of Heidelberg, Heidelberg, Germany.
Peter SchmezerDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Heribert RamrothInstitute of Public Health, University of Heidelberg, Heidelberg, Germany.
Odilia PopandaDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany. o.popanda@dkfz.de.ORCID 0000-0002-5594-5736
German Cancer Research Center · DEHeidelberg University · DEKlinikum Darmstadt · DEKlinikum Ludwigshafen · DEQueen Mary Hospital · CNChulabhorn Research Institute · THHeilbronn University · DELeipzig University · DEUniversität Hamburg · DEUniversity Medical Centre Mannheim · DEUniversity of Mannheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenetic aberrations in DNA repair genes are linked to cancer, but less is reported about epigenetic regulation of DNA repair and functional consequences. We investigated the intragenic methylation loss at the three prime repair exonuclease 2 (TREX2) locus in laryngeal (n = 256) and colorectal cancer cases (n = 95) and in pan-cancer data from The Cancer Genome Atlas (TCGA).

resultsSignificant methylation loss at an intragenic site of TREX2 was a frequent trait in both patient cohorts (p = 0.016 and < 0.001, respectively) and in 15 out of 22 TCGA studies. Methylation loss correlated with immunohistochemically staining for TREX2 (p < 0.0001) in laryngeal tumors and improved overall survival of laryngeal cancer patients (p = 0.045). Chromatin immunoprecipitation, demethylation experiments, and reporter gene assays revealed that the region of methylation loss can function as a CCAAT/enhancer binding protein alpha (CEBPA)-responsive enhancer element regulating TREX2 expression.

conclusionsThe data highlight a regulatory role of TREX2 DNA methylation for gene expression which might affect incidence and survival of laryngeal cancer. Altered TREX2 protein levels in tumors may affect drug-induced DNA damage repair and provide new tailored therapies.

Indexed as

DNA MethylationUp-RegulationAgedCell Line, TumorDNA RepairEpigenesis, GeneticExodeoxyribonucleasesFemaleGene Expression Regulation, NeoplasticHCT116 CellsHumansLaryngeal NeoplasmsMaleMiddle AgedPhosphoproteinsProtein DomainsExodeoxyribonucleasesPhosphoproteinsTREX2 protein, humanDNA methylationDNA repairEpigeneticsHead and neck cancerHNSCCLaryngeal cancerPan-cancer studiesPatient survivalTCGATREX2

Identifiers

PMID31053176
PMCPMC6499986
OpenAlexW2947097770

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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.