Evidence map›Paper›PMID 32437908›Full record

ArticleExperimental hematology2020

Epigenetic regulation of protein translation in KMT2A-rearranged AML.

Alexandra Lenard, Hongbo Michael Xie, Taylor Pastuer, Tyler Shank, Clara Libbrecht, Molly Kingsley, Simone S Riedel, Zuo-Fei Yuan, Nan Zhu, Tobias Neff and 1 more

Open access · greenAbstract read
In one paragraph

Article in Experimental hematology, 2020. 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
1.3field-weighted citation impact, top 18% 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, 14 citations in OpenAlex.

  1. Article
  2. Genomic Characteristics of Bladder Cancer: An AACR Project GENIE Study.International journal of molecular sciences · 2025
    Article
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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

11 authors at 3 institutions in 1 country.

Alexandra LenardDivision of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.
Hongbo Michael XieDivision of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.
Taylor PastuerDivision of Pediatric Hematology/Oncology/BMT, University of Colorado School of Medicine and Children's Hospital Colorado Aurora, CO.
Tyler ShankDivision of Pediatric Hematology/Oncology/BMT, University of Colorado School of Medicine and Children's Hospital Colorado Aurora, CO.
Clara LibbrechtDivision of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.
Molly KingsleyDivision of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.
Simone S RiedelDivision of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.
Zuo-Fei YuanDivision of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.
Nan ZhuStem Cell Biology and Hematopoiesis Program, Blood Research Institute, Blood Center of Wisconsin, Milwaukee, WI; Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI.
Tobias NeffDivision of Pediatric Hematology/Oncology/BMT, University of Colorado School of Medicine and Children's Hospital Colorado Aurora, CO.
Kathrin M BerntDivision of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania and Abramson Cancer Center, Philadelphia, PA. Electronic address: berntk@email.chop.edu.
Children's Hospital of Philadelphia · USChildren's Hospital Colorado · USMedical College of Wisconsin · US

Funding

The histone demethylase JMJD1C in human Acute Myeloid LeukemiaR37CA229751 · NCI · VERSITI WISCONSIN, INC. · PI ZHU, NAN · 2019 to 2025
$2.9M
The role of H3K79 methylation in IDH-mutant leukemiaR01CA201230 · NCI · UNIVERSITY OF COLORADO DENVER · PI BERNT, KATHRIN M · 2016 to 2020
$2.2M
H3K79 Methylation in Hematopoietic Stem Cell Development and MLL-Rearranged LeukK08HL102264 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI BERNT, KATHRIN M · 2010 to 2014
$660k
NCI NIH HHS R01 CA201230NCI NIH HHS R37 CA229751NHLBI NIH HHS K08 HL102264
6 · The paper itself

Abstract

Inhibition of the H3K79 histone methyltransferase DOT1L has exhibited encouraging preclinical and early clinical activity in KMT2A (MLL)-rearranged leukemia, supporting the development of combinatorial therapies. Here, we investigated two novel combinations: dual inhibition of the histone methyltransferases DOT1L and EZH2, and the combination with a protein synthesis inhibitor. EZH2 is the catalytic subunit in the polycomb repressive complex 2 (PRC2), and inhibition of EZH2 has been reported to have preclinical activity in KMT2A-r leukemia. When combined with DOT1L inhibition, however, we observed both synergistic and antagonistic effects. Interestingly, antagonistic effects were not due to PRC2-mediated de-repression of HOXA9. HOXA cluster genes are key canonical targets of both KMT2A and the PRC2 complex. The independence of the HOXA cluster from PRC2 repression in KMT2A-r leukemia thus affords important insights into leukemia biology. Further studies revealed that EZH2 inhibition counteracted the effect of DOT1L inhibition on ribosomal gene expression. We thus identified a previously unrecognized role of DOT1L in regulating protein production. Decreased translation was one of the earliest effects measurable after DOT1L inhibition and specific to KMT2A-rearranged cell lines. H3K79me2 chromatin immunoprecipitation sequencing patterns over ribosomal genes were similar to those of the canonical KMT2A-fusion target genes in primary AML patient samples. The effects of DOT1L inhibition on ribosomal gene expression prompted us to evaluate the combination of EPZ5676 with a protein translation inhibitor. EPZ5676 was synergistic with the protein translation inhibitor homoharringtonine (omacetaxine), supporting further preclinical/clinical development of this combination. In summary, we discovered a novel epigenetic regulation of a metabolic process-protein synthesis-that plays a role in leukemogenesis and affords a combinatorial therapeutic opportunity.

Indexed as

Epigenesis, GeneticGene Expression Regulation, LeukemicGene RearrangementProtein BiosynthesisCell Line, TumorEnhancer of Zeste Homolog 2 ProteinHistone-Lysine N-MethyltransferaseHomeodomain ProteinsHumansLeukemia, Myeloid, AcuteMyeloid-Lymphoid Leukemia ProteinPolycomb Repressive Complex 2DOT1L protein, humanEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHistone-Lysine N-Methyltransferasehomeobox protein HOXA9Homeodomain ProteinsKMT2A protein, humanMyeloid-Lymphoid Leukemia ProteinPolycomb Repressive Complex 2

Identifiers

PMID32437908
PMCPMC8362846
OpenAlexW3021539898

What OpenQuestion holds

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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.