Evidence map›Paper›PMID 30945122›Full record

ArticleMolecular imaging and biology2019

Impact of rs12917 MGMT Polymorphism on [

Stefanie Kewitz-Hempel, Lars Kurch, Michaela Cepelova, Ines Volkmer, Axel Sauerbrey, Elke Conrad, Stephanie Knirsch, Gabriele Pöpperl, Daniel Steinbach, Ambros J Beer and 8 more

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Article in Molecular imaging and biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

18 authors at 10 institutions in 2 countries.

Stefanie Kewitz-HempelDepartment of Pediatrics I, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle, Germany.
Lars KurchDepartment of Nuclear Medicine, University Hospital of Leipzig, 04103, Leipzig, Germany.
Michaela CepelovaDepartment of Pediatric Hematology and Oncology, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Praha, Czech Republic.
Ines VolkmerDepartment of Pediatrics I, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle, Germany.
Axel SauerbreyHelios Childrens Hospital, Erfurt, Germany.
Elke ConradDepartment of Nuclear Medicine, Helios Hospital Erfurt, Erfurt, Germany.
Stephanie KnirschPediatrics 5 (Oncology, Hematology, and Immunology), Klinikum Stuttgart, Olgahospital, Stuttgart, Germany.
Gabriele PöpperlDepartment of Nuclear Medicine, Klinikum Stuttgart, Olgahospital, Stuttgart, Germany.
Daniel SteinbachDepartment of Pediatric Hematology and Oncology, University Hospital Ulm, Ulm, Germany.
Ambros J BeerDepartment of Nuclear Medicine, University Hospital, Ulm, Germany.
Christof M KrammDepartment of Pediatrics I, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle, Germany.
Carsten-Oliver SahlmannDepartment of Nuclear Medicine, Georg August University, Göttingen, Germany.
Bernhard ErdlenbruchUniversity Hospital for Children and Adolescents, Johannes Wesling Klinikum Minden, Ruhr University Hospital, Bochum, Germany.
Wolf-Dieter ReinboldUniversitätsinstitut für Diagnostische Radiologie, Neuroradiologie und Nuklearmedizin, Johannes Wesling Klinikum Minden, Ruhr University Hospital, Bochum, Germany.
Andreas OdparlikDepartment of Nuclear Medicine, Martin Luther University Halle-Wittenberg, Halle, Germany.
Osama SabriDepartment of Nuclear Medicine, University Hospital of Leipzig, 04103, Leipzig, Germany.
Regine KlugeDepartment of Nuclear Medicine, University Hospital of Leipzig, 04103, Leipzig, Germany. Regine.Kluge@medizin.uni-leipzig.de.
Martin S StaegeDepartment of Pediatrics I, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle, Germany. martin.staege@medizin.uni-halle.de.ORCID http://orcid.org/0000-0003-3765-7068
Martin Luther University Halle-Wittenberg · DEUniversity Hospital Leipzig · DEHelios Klinikum Erfurt · DEJohannes Wesling Klinikum Minden · DEOlgahospital · DEUniversity Hospital Ulm · DECharles University · CZJustus-Liebig-Universität Gießen · DEUniversitätsmedizin Göttingen · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe enzyme O6-methylguanine-DNA methyltransferase (MGMT) is an important component of the DNA repair machinery. MGMT removes O6-methylguanine from the DNA by transferring the methyl group to a cysteine residue in its active site. Recently, we detected the single nucleotide polymorphism (SNP) rs12917 (C/T) in the MGMT sequence adjacent to the active site in Hodgkin lymphoma (HL) cell line KM-H2. We now investigated whether this SNP is also present in other HL cell lines and patient samples. Furthermore, we asked whether this SNP might have an impact on metabolic response in 2-deoxy-2-[ PROCEDURES: We determined the frequency of this MGMT polymorphism in 5 HL cell lines and in 29 pediatric HL (PHL) patients. The patient cohort included 17 female and 12 male patients aged between 4 and 18 years. After characterization of the sequence, we tested a possible association between rs12917 and age, gender, Ann Arbor stage, treatment group, metabolic response following two courses of OEPA (vincristine, etoposide, prednisone, and doxorubicin) chemotherapy, radiotherapy indication, and relapse status.

resultsWe detected the minor T allele in four of five HL cell lines. 11/29 patients carried the minor T allele whereas 18/29 patients showed homozygosity for the major C allele. Interestingly, we observed significantly better metabolic response in PHL patients carrying the rs12917 C allele resulting in a lower frequency of radiotherapy indication.

conclusionMGMT polymorphism rs12917 seems to affect chemotherapy response in PHL. The prognostic value of this polymorphism should be investigated in a larger patient cohort.

Indexed as

Positron-Emission TomographyAdolescentBase SequenceCell Line, TumorChildChild, PreschoolDNA Modification MethylasesDNA Repair EnzymesFemaleFluorodeoxyglucose F18Hodgkin DiseaseHumansMalePolymorphism, Single NucleotideTumor Suppressor ProteinsDNA Modification MethylasesDNA Repair EnzymesFluorodeoxyglucose F18MGMT protein, humanTumor Suppressor Proteins[18F]FDG-PETDeauville scoreMGMTPediatric Hodgkin lymphomaqPETrs12917

Identifiers

PMID30945122
OpenAlexW2933168584

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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.