Evidence map›Paper›PMID 32389825›Full record

ReviewBiochimica et biophysica acta. Gene regulatory mechanisms2020

The MLL/SET family and haematopoiesis.

Eric T B Antunes, Katrin Ottersbach

Open access · hybridAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Gene regulatory mechanisms, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Expanded profiling of WD repeat domain 5 inhibitors reveals actionable strategies for the treatment of hematologic malignancies.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
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  11. Article
  12. Clinical profile inFrontiers in medicine · 2022
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. 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

2 authors at 2 institutions in 1 country.

Eric T B AntunesMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, Scotland, UK.
Katrin OttersbachMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, Scotland, UK. Electronic address: katrin.ottersbach@ed.ac.uk.
MRC Centre for Regenerative Medicine · GBUniversity of Edinburgh · GB

Funding

Cancer Research UK 23581Wellcome Trust
6 · The paper itself

Abstract

As demonstrated through early work in Drosophila, members of the MLL/SET family play essential roles during embryonic development through their participation in large protein complexes that are central to epigenetic regulation of gene expression. One of its members, MLL1, has additionally received a lot of attention as it is a potent oncogenic driver in different types of leukaemia when aberrantly fused to a large variety of partners as a result of chromosomal translocations. Its exclusive association with cancers of the haematopoietic system has prompted a large number of investigations into the role of MLL/SET proteins in haematopoiesis, a summary of which was attempted in this review. Interestingly, MLL-rearranged leukaemias are particularly prominent in infant and paediatric leukaemia, which commonly initiate in utero. This, together with the known function of MLL/SET proteins in embryonic development, has focussed research efforts in recent years on understanding the role of this protein family in developmental haematopoiesis and how this may be subverted by MLL oncofusions in infant leukaemia. A detailed understanding of these prenatal events is essential for the development of new treatments that improve the survival specifically of this very young patient group.

Indexed as

AnimalsChildDNA-Binding ProteinsEmbryonic DevelopmentEpigenesis, GeneticHematopoiesisHistone-Lysine N-MethyltransferaseHumansInfantLeukemiaMyeloid-Lymphoid Leukemia ProteinNeoplasm ProteinsDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseKMT2A protein, humanKMT2C protein, humanKMT2D protein, humanMLL4 protein, humanMyeloid-Lymphoid Leukemia ProteinNeoplasm ProteinsSetd1A protein, humanSETD1B protein, human

Identifiers

PMID32389825
PMCPMC7294230
OpenAlexW3023934964

What OpenQuestion 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 OpenQuestion graph.