Evidence map›Paper›PMID 28824170›Full record

ArticleLeukemia2018

Differences between BCL2-break positive and negative follicular lymphoma unraveled by whole-exome sequencing.

A Zamò, J Pischimarov, M Schlesner, P Rosenstiel, R Bomben, H Horn, T Grieb, T Nedeva, C López, A Haake and 15 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-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

15 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Follicular lymphoma.Nature reviews. Disease primers · 2019
    Review
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  15. Review
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

25 authors at 13 institutions in 2 countries.

A ZamòInstitute of Pathology, University of Würzburg, Würzburg, Würzburg, Germany.
J PischimarovInstitute of Pathology, University of Würzburg, Würzburg, Würzburg, Germany.
M SchlesnerTheoretical Bioinformatics (B080), Computational Oncology Group, German Cancer Research Center (DKFZ), Heidelberg, Germany.
P RosenstielInstitute for Clinical Molecular Biology, Christian-Albrechts-University, Kiel, Germany.
R BombenDepartment of Translational Research, CRO, Aviano, Italy.
H HornDr Margarete Fischer-Bosch-Institute for Clinical Pharmacology, Stuttgart, Germany.
T GriebInstitute of Pathology, University of Würzburg, Würzburg, Würzburg, Germany.
T NedevaInstitute of Pathology, University of Würzburg, Würzburg, Würzburg, Germany.
C LópezInstitute for Human Genetics, University Hospital Ulm, Ulm, Germany.
A HaakeInstitute for Human Genetics, University Hospital Schleswig-Holstein, Kiel, Germany.
J RichterInstitute for Human Genetics, University Hospital Schleswig-Holstein, Kiel, Germany.
L TrümperDepartment of Hematology and Medical Oncology, University Hospital, Göttingen, Germany.
C LawerenzTheoretical Bioinformatics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
W KlapperInstitute of Pathology, University Hospital Schleswig-Holstein, Kiel, Germany.
P MöllerInstitute of Pathology, University Hospital Ulm, Ulm, Germany.
M HummelInstitute of Pathology, Charité-University Hospital Berlin, Germany.
D LenzeInstitute of Pathology, Charité-University Hospital Berlin, Germany.
M SzczepanowskiInstitute of Pathology, University Hospital Schleswig-Holstein, Kiel, Germany.
L FlossbachInstitute of Pathology, University of Würzburg, Würzburg, Würzburg, Germany.
M SchrederMedizinische Klinik und Poliklinik II, University Hospital Würzburg, Würzburg, Germany.
V GatteiDepartment of Translational Research, CRO, Aviano, Italy.
G OttDepartment of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart, Germany.
R SiebertInstitute for Human Genetics, University Hospital Ulm, Ulm, Germany.
A RosenwaldInstitute of Pathology, University of Würzburg, Würzburg, Würzburg, Germany.
E LeichInstitute of Pathology, University of Würzburg, Würzburg, Würzburg, Germany.
Comprehensive Cancer Center Mainfranken · DEUniversity Hospital Schleswig-Holstein · DECentro di Riferimento Oncologico · ITCharité - Universitätsmedizin Berlin · DEHeidelberg University · DEUniversity Hospital Ulm · DEUniversity of Lübeck · DEUniversity of Würzburg · DEDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology · DEKiel University · DERobert Bosch Hospital · DEUniversitätsklinikum Würzburg · DEUniversitätsmedizin Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depending on disease stage follicular lymphoma (FL) lack the t(14;18) in ~15-~50% of cases. Nevertheless, most of these cases express BCL2. To elucidate mechanisms triggering BCL2 expression and promoting pathogenesis in t(14;18)-negative FL, exonic single-nucleotide variant (SNV) profiles of 28 t(14;18)-positive and 13 t(14;18)-negative FL were analyzed, followed by the integration of copy-number changes, copy-neutral LOH and published gene-expression data as well as the assessment of immunoglobulin N-glycosylation sites. Typical FL mutations also affected t(14;18)-negative FL. Curated gene set/pathway annotation of genes mutated in either t(14;18)-positive or t(14;18)-negative FL revealed a strong enrichment of same or similar gene sets but also a more prominent or exclusive enrichment of immune response and N-glycosylation signatures in t(14;18)-negative FL. Mutated genes showed high BCL2 association in both subgroups. Among the genes mutated in t(14;18)-negative FL 555 were affected by copy-number alterations and/or copy-neutral LOH and 96 were differently expressed between t(14;18)-positive and t(14;18)-negative FL (P<0.01). N-glycosylation sites were detected considerably less frequently in t(14;18)-negative FL. These results suggest a diverse portfolio of genetic alterations that may induce or regulate BCL2 expression or promote pathogenesis of t(14;18)-negative FL as well as a less specific but increased crosstalk with the microenvironment that may compensate for the lack of N-glycosylation.

Indexed as

Biomarkers, TumorChromosomes, Human, Pair 14Chromosomes, Human, Pair 18Computational BiologyDNA Copy Number VariationsExome SequencingGlycosylationHumansImmunoglobulin Variable RegionLymphoma, FollicularMutationPolymorphism, Single NucleotideProto-Oncogene Proteins c-bcl-2Translocation, GeneticBiomarkers, TumorImmunoglobulin Variable RegionProto-Oncogene Proteins c-bcl-2

Identifiers

PMID28824170
OpenAlexW2746594801

What OpenQuestion holds

Textmetadata
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.