Evidence map›Paper›PMID 19395026›Full record

ArticleLeukemia research2009

OH-2, a hyperdiploid myeloma cell line without an IGH translocation, has a complex translocation juxtaposing MYC near MAFB and the IGK locus.

Thea Kristin Våtsveen, Erming Tian, Stine H Kresse, Leonardo A Meza-Zepeda, Ana Gabrea, Oleg Glebov, Hong Yan Dai, Anders Sundan, W Michael Kuehl, Magne Børset

Abstract read
In one paragraph

Article in Leukemia research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

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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

10 authors.

Thea Kristin VåtsveenDepartment of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway. thea.k.vatsveen@ntnu.no
Erming Tian
Stine H Kresse
Leonardo A Meza-Zepeda
Ana Gabrea
Oleg Glebov
Hong Yan Dai
Anders Sundan
W Michael Kuehl
Magne Børset

Funding

Genomic Rearrangements in Multiple MyelomaZIABC010910 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KUEHL, WALTER · 2009 to 2015
$3.8M
Genomic Rearrangements in Multiple MyelomaZ01BC010910 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KUEHL, WALTER · 2008 to 2008
$615k
Intramural NIH HHS Z01 BC010910
6 · The paper itself

Abstract

Multiple myeloma can be classified into hyperdiploid (HRD) (with 48-74 chromosomes) and non-hyperdiploid tumors (usually with immunoglobulin heavy chain translocations). The OH-2 human myeloma cell line (HMCL) retains the same HRD genotype as the primary tumor, with extra copies of chromosomes 3, 7, 15, 19, and 21. Both OH-2 and primary cells have a complex secondary translocation in which the IGK 3' enhancer is inserted between MYC and MAFB, resulting in dysregulation of both oncogenes. OH-2 provides a unique example of an HMCL and the corresponding primary tumor that are shown to share the same HRD genotype.

Indexed as

Genes, mycTranslocation, GeneticCell Line, TumorDiploidyEnhancer Elements, GeneticGenotypeHumansImmunoglobulin Heavy ChainsImmunoglobulin kappa-ChainsIn Situ Hybridization, FluorescenceKaryotypingMafB Transcription FactorMultiple MyelomaReverse Transcriptase Polymerase Chain ReactionRNA, MessengerImmunoglobulin Heavy ChainsImmunoglobulin kappa-ChainsMAFB protein, humanMafB Transcription FactorRNA, Messenger

Identifiers

PMID19395026
PMCPMC6944273

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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.