Evidence map›Paper›PMID 22411814›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Myeloid leukemia factor is a conserved regulator of RUNX transcription factor activity involved in hematopoiesis.

Stéphanie Bras, Séverine Martin-Lannerée, Vanessa Gobert, Benoît Augé, Osman Breig, Matthieu Sanial, Masamitsu Yamaguchi, Marc Haenlin, Anne Plessis, Lucas Waltzer

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  7. The Role of Lozenge inMolecules and cells · 2020
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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 at 5 institutions in 2 countries.

Stéphanie BrasCentre National de la Recherche Scientifique, Unité Mixte de Recherche 5547, Université de Toulouse, 31062 Toulouse, France.
Séverine Martin-Lannerée
Vanessa Gobert
Benoît Augé
Osman Breig
Matthieu Sanial
Masamitsu Yamaguchi
Marc Haenlin
Anne Plessis
Lucas Waltzer
Centre de Biologie du Développement · FRInstitut Jacques Monod · FRUniversité de Toulouse · FRKyoto Institute of Technology · JPUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defining the function of the genes that, like RUNX1, are deregulated in blood cell malignancies represents an important challenge. Myeloid leukemia factors (MLFs) constitute a poorly characterized family of conserved proteins whose founding member, MLF1, has been associated with acute myeloid leukemia in humans. To gain insight into the functions of this family, we investigated the role of the Drosophila MLF homolog during blood cell development. Here we report that mlf controls the homeostasis of the Drosophila hematopoietic system. Notably, mlf participates in a positive feedback loop to fine tune the activity of the RUNX transcription factor Lozenge (LZ) during development of the crystal cells, one of the two main blood cell lineages in Drosophila. At the molecular level, our data in cell cultures and in vivo strongly suggest that MLF controls the number of crystal cells by protecting LZ from degradation. Remarkably, it appears that the human MLF1 protein can substitute for MLF in the crystal cell lineage. In addition, MLF stabilizes the human oncogenic fusion protein RUNX1-ETO and is required for RUNX1-ETO-induced blood cell disorders in a Drosophila model of leukemia. Finally, using the human leukemic blood cell line Kasumi-1, we show that MLF1 depletion impairs RUNX1-ETO accumulation and reduces RUNX1-ETO-dependent proliferation. Thus, we propose that the regulation of RUNX protein levels is a conserved feature of MLF family members that could be critical for normal and pathological blood cell development.

Indexed as

HematopoiesisAnimalsCell LineageConserved SequenceCore Binding Factor Alpha 2 SubunitCore Binding Factor alpha SubunitsDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianHumansLarvaOncogene Proteins, FusionPhenotypeProtein StabilityProteolysisCore Binding Factor Alpha 2 SubunitCore Binding Factor alpha SubunitsDNA-Binding ProteinsDrosophila Proteinslz protein, DrosophilaMlf protein, DrosophilaOncogene Proteins, FusionRUNX1 protein, humanTranscription Factors

Identifiers

PMID22411814
PMCPMC3324030
OpenAlexW2085625111

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.