Evidence map›Paper›PMID 34383740›Full record

ArticlePLoS genetics2021

A genetic screen in Drosophila uncovers the multifaceted properties of the NUP98-HOXA9 oncogene.

Gwenaëlle Gavory, Caroline Baril, Gino Laberge, Gawa Bidla, Surapong Koonpaew, Thomas Sonea, Guy Sauvageau, Marc Therrien

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 1 institution in 1 country.

Gwenaëlle GavoryInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Caroline BarilInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.ORCID 0000-0002-2226-5988
Gino LabergeInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Gawa BidlaInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Surapong KoonpaewInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.ORCID 0000-0003-3817-2118
Thomas SoneaInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Guy SauvageauInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.ORCID 0000-0002-4333-7266
Marc TherrienInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.ORCID 0000-0003-2047-7650
Institute for Research in Immunology and Cancer · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) underlies the uncontrolled accumulation of immature myeloid blasts. Several cytogenetic abnormalities have been associated with AML. Among these is the NUP98-HOXA9 (NA9) translocation that fuses the Phe-Gly repeats of nucleoporin NUP98 to the homeodomain of the transcription factor HOXA9. The mechanisms enabling NA9-induced leukemia are poorly understood. Here, we conducted a genetic screen in Drosophila for modifiers of NA9. The screen uncovered 29 complementation groups, including genes with mammalian homologs known to impinge on NA9 activity. Markedly, the modifiers encompassed a diversity of functional categories, suggesting that NA9 perturbs multiple intracellular events. Unexpectedly, we discovered that NA9 promotes cell fate transdetermination and that this phenomenon is greatly influenced by NA9 modifiers involved in epigenetic regulation. Together, our work reveals a network of genes functionally connected to NA9 that not only provides insights into its mechanism of action, but also represents potential therapeutic targets.

Indexed as

AnimalsCell DifferentiationDrosophila melanogasterEpigenesis, GeneticGene ExpressionGene Expression RegulationGene Regulatory NetworksHomeodomain ProteinsHumansLeukemia, Myeloid, AcuteMyeloid CellsNuclear Pore Complex ProteinsOncogene Proteins, FusionOncogenesTranscription FactorsTranslocation, Genetichomeobox protein HOXA9Homeodomain Proteinsnuclear pore complex protein 98Nuclear Pore Complex ProteinsNUP98-HOXA9 fusion protein, humanOncogene Proteins, FusionTranscription Factors

Identifiers

PMID34383740
PMCPMC8384169
OpenAlexW3190953477

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.