Evidence map›Paper›PMID 27390358›Full record

ArticleHaematologica2016

Alterations of microRNA and microRNA-regulated messenger RNA expression in germinal center B-cell lymphomas determined by integrative sequencing analysis.

Kebria Hezaveh, Andreas Kloetgen, Stephan H Bernhart, Kunal Das Mahapatra, Dido Lenze, Julia Richter, Andrea Haake, Anke K Bergmann, Benedikt Brors, Birgit Burkhardt and 36 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.0field-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

36 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
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  4. microRNA Profile of High-Grade B-Cell Lymphoma with 11q Aberration.International journal of molecular sciences · 2024
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  12. Consequences of genetic variants in miRNA genes.Computational and structural biotechnology journal · 2022
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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

46 authors at 20 institutions in 2 countries.

Kebria HezavehDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Heinrich-Heine-University, Medical Faculty, Düsseldorf, Germany.
Andreas KloetgenDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Heinrich-Heine-University, Medical Faculty, Düsseldorf, Germany.
Stephan H BernhartTranscriptome Bioinformatics Group, LIFE Research Center for Civilization Diseases, University of Leipzig, Germany.
Kunal Das MahapatraDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Heinrich-Heine-University, Medical Faculty, Düsseldorf, Germany.
Dido LenzeInstitute of Pathology, Charité - University Medicine Berlin, Germany.
Julia RichterInstitute of Human Genetics, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Andrea HaakeInstitute of Human Genetics, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Anke K BergmannInstitute of Human Genetics, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Benedikt BrorsDivision Applied Bioinformatics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Birgit BurkhardtDepartment of Pediatric Hematology and Oncology, University Hospital Münster, Germany.
Alexander ClaviezDepartment of Pediatrics, University Hospital Schleswig-Holstein, Campus Kiel, Germany.
Hans G DrexlerDepartment of Human and Animal Cell Cultures, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Roland EilsDivision of Theoretical Bioinformatics (B080), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Siegfried HaasFriedrich-Ebert Hospital Neumünster, Clinics for Hematology, Oncology and Nephrology, Neumünster, Germany.
Steve HoffmannTranscriptome Bioinformatics Group, LIFE Research Center for Civilization Diseases, University of Leipzig, Germany.
Dennis KarschDepartment of Internal Medicine II: Hematology and Oncology, University Medical Centre, Campus Kiel, Germany.
Wolfram KlapperHematopathology Section, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Kortine KleinheinzDivision of Theoretical Bioinformatics (B080), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Jan KorbelEMBL Heidelberg, Genome Biology, Heidelberg, Germany.
Helene KretzmerTranscriptome Bioinformatics Group, LIFE Research Center for Civilization Diseases, University of Leipzig, Germany.
Markus KreuzInstitute for Medical Informatics Statistics and Epidemiology, Leipzig, Germany.
Ralf KüppersInstitute of Cell Biology (Cancer Research), University of Duisburg-Essen, Essen, Germany.
Chris LawerenzDivision of Theoretical Bioinformatics (B080), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Ellen LeichInstitute of Pathology, University of Würzburg, and Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Markus LoefflerInstitute for Medical Informatics Statistics and Epidemiology, Leipzig, Germany.
Luisa Mantovani-LoefflerHospital of Internal Medicine II, Hematology and Oncology, St-Georg Hospital Leipzig, Germany.
Cristina LópezInstitute of Human Genetics, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Alice C McHardyDepartment of Algorithmic Bioinformatics, Heinrich-Heine University, Duesseldorf, Germany.
Peter MöllerInstitute of Pathology, Medical Faculty of the Ulm University, Germany.
Marius RohdeDepartment of Pediatric Hematology and Oncology University Hospital Giessen, Germany.
Philip RosenstielInstitute of Clinical Molecular Biology, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Andreas RosenwaldInstitute of Pathology, University of Würzburg, and Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Markus SchilhabelInstitute of Clinical Molecular Biology, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Matthias SchlesnerDivision of Theoretical Bioinformatics (B080), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Ingrid ScholzDivision of Theoretical Bioinformatics (B080), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Peter F StadlerTranscriptome Bioinformatics Group, LIFE Research Center for Civilization Diseases, University of Leipzig, Germany.
Stephan StilgenbauerDepartment of Internal Medicine III, University of Ulm, Germany.
Stéphanie SungaleeEMBL Heidelberg, Genome Biology, Heidelberg, Germany.
Monika SzczepanowskiHematopathology Section, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Lorenz TrümperDepartment of Hematology and Oncology, Georg-August-University of Göttingen, Germany.
Marc A WenigerInstitute of Cell Biology (Cancer Research), University of Duisburg-Essen, Essen, Germany.
Reiner SiebertInstitute of Human Genetics, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
Arndt BorkhardtDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Heinrich-Heine-University, Medical Faculty, Düsseldorf, Germany.
Michael HummelInstitute of Pathology, Charité - University Medicine Berlin, Germany.
Jessica I Hoell
ICGC MMML-Seq Project
Heinrich Heine University Düsseldorf · DELeipzig University · DEUniversity Hospital Schleswig-Holstein · DEUniversity of Lübeck · DEGerman Cancer Research Center · DECharité - Universitätsmedizin Berlin · DEChristian-Albrechts-Universität zu Kiel · DEHeidelberg University · DEUniversität Ulm · DEUniversity of Duisburg-Essen · DEClinical Research Center Kiel · DEComprehensive Cancer Center Mainfranken · DEDeutschen Konsortium für Translationale Krebsforschung · DEFriedrich-Ebert-Krankenhaus · DEHelmholtz Centre for Infection Research · DEKlinikum St. Georg · DELeibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures · DEUniversitätsklinikum Gießen und Marburg · DEUniversity Hospital Münster · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA are well-established players in post-transcriptional gene regulation. However, information on the effects of microRNA deregulation mainly relies on bioinformatic prediction of potential targets, whereas proof of the direct physical microRNA/target messenger RNA interaction is mostly lacking. Within the International Cancer Genome Consortium Project "Determining Molecular Mechanisms in Malignant Lymphoma by Sequencing", we performed miRnome sequencing from 16 Burkitt lymphomas, 19 diffuse large B-cell lymphomas, and 21 follicular lymphomas. Twenty-two miRNA separated Burkitt lymphomas from diffuse large B-cell lymphomas/follicular lymphomas, of which 13 have shown regulation by MYC. Moreover, we found expression of three hitherto unreported microRNA. Additionally, we detected recurrent mutations of hsa-miR-142 in diffuse large B-cell lymphomas and follicular lymphomas, and editing of the hsa-miR-376 cluster, providing evidence for microRNA editing in lymphomagenesis. To interrogate the direct physical interactions of microRNA with messenger RNA, we performed Argonaute-2 photoactivatable ribonucleoside-enhanced cross-linking and immunoprecipitation experiments. MicroRNA directly targeted 208 messsenger RNA in the Burkitt lymphomas and 328 messenger RNA in the non-Burkitt lymphoma models. This integrative analysis discovered several regulatory pathways of relevance in lymphomagenesis including Ras, PI3K-Akt and MAPK signaling pathways, also recurrently deregulated in lymphomas by mutations. Our dataset reveals that messenger RNA deregulation through microRNA is a highly relevant mechanism in lymphomagenesis.

Indexed as

AdolescentBurkitt LymphomaChildChild, PreschoolFemaleGene Expression ProfilingGerminal CenterHumansInfantInfant, NewbornLymphoma, B-CellLymphoma, FollicularLymphoma, Large B-Cell, DiffuseMaleMicroRNAsMutationMicroRNAsMIRN142 microRNA, humanMIRN376C microRNA, humanRNA, Messenger

Identifiers

PMID27390358
PMCPMC5394868
OpenAlexW2541856909

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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.