Evidence map›Paper›PMID 24147083›Full record

ArticlePloS one2013

Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.

Thorsten Klampfl, Jelena D Milosevic, Ana Puda, Andreas Schönegger, Klaudia Bagienski, Tiina Berg, Ashot S Harutyunyan, Bettina Gisslinger, Elisa Rumi, Luca Malcovati and 18 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. A microglia clonal inflammatory disorder in Alzheimer's Disease.bioRxiv : the preprint server for biology · 2024
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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

28 authors at 10 institutions in 4 countries.

Thorsten KlampflCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Jelena D Milosevic
Ana Puda
Andreas Schönegger
Klaudia Bagienski
Tiina Berg
Ashot S Harutyunyan
Bettina Gisslinger
Elisa Rumi
Luca Malcovati
Daniela Pietra
Chiara Elena
Matteo Giovanni Della Porta
Lisa Pieri
Paola Guglielmelli
Christoph Bock
Michael Doubek
Dana Dvorakova
Nada Suvajdzic
Dragica Tomin
Natasa Tosic
Zdenek Racil
Michael Steurer
Sonja Pavlovic
Alessandro M Vannucchi
Mario Cazzola
Heinz Gisslinger
Robert Kralovics
Austrian Academy of Sciences · ATCeMM Research Center for Molecular Medicine · ATIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Belgrade · RSUniversity of Florence · ITCentral European Institute of Technology · CZMedical University of Vienna · ATPoliclinico San Matteo Fondazione · ITMasaryk University · CZUniversity Hospital Innsbruck · AT

Funding

Austrian Science Fund FWF P 23257
6 · The paper itself

Abstract

Exome sequencing of primary tumors identifies complex somatic mutation patterns. Assignment of relevance of individual somatic mutations is difficult and poses the next challenge for interpretation of next generation sequencing data. Here we present an approach how exome sequencing in combination with SNP microarray data may identify targets of chromosomal aberrations in myeloid malignancies. The rationale of this approach is that hotspots of chromosomal aberrations might also harbor point mutations in the target genes of deletions, gains or uniparental disomies (UPDs). Chromosome 11 is a frequent target of lesions in myeloid malignancies. Therefore, we studied chromosome 11 in a total of 813 samples from 773 individual patients with different myeloid malignancies by SNP microarrays and complemented the data with exome sequencing in selected cases exhibiting chromosome 11 defects. We found gains, losses and UPDs of chromosome 11 in 52 of the 813 samples (6.4%). Chromosome 11q UPDs frequently associated with mutations of CBL. In one patient the 11qUPD amplified somatic mutations in both CBL and the DNA repair gene DDB1. A duplication within MLL exon 3 was detected in another patient with 11qUPD. We identified several common deleted regions (CDR) on chromosome 11. One of the CDRs associated with de novo acute myeloid leukemia (P=0.013). One patient with a deletion at the LMO2 locus harbored an additional point mutation on the other allele indicating that LMO2 might be a tumor suppressor frequently targeted by 11p deletions. Our chromosome-centered analysis indicates that chromosome 11 contains a number of tumor suppressor genes and that the role of this chromosome in myeloid malignancies is more complex than previously recognized.

Indexed as

Chromosome AberrationsAdaptor Proteins, Signal TransducingChromosomes, Human, Pair 11DNA-Binding ProteinsExomeHistone-Lysine N-MethyltransferaseHumansLeukemia, Myeloid, AcuteLIM Domain ProteinsMyelodysplastic SyndromesMyeloid-Lymphoid Leukemia ProteinPolycythemia VeraPolymerase Chain ReactionPrimary MyelofibrosisProto-Oncogene ProteinsProto-Oncogene Proteins c-cblAdaptor Proteins, Signal TransducingCBL protein, humanDDB1 protein, humanDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseKMT2A protein, humanLIM Domain ProteinsLMO2 protein, humanMyeloid-Lymphoid Leukemia ProteinProto-Oncogene ProteinsProto-Oncogene Proteins c-cbl

Identifiers

PMID24147083
PMCPMC3797696
OpenAlexW2051570543

What OpenQuestion holds

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Read underepoch 390

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.