Evidence map›Paper›PMID 35538058›Full record

ArticleCell death & disease2022

Hexokinase 3 enhances myeloid cell survival via non-glycolytic functions.

Kristina Seiler, Magali Humbert, Petra Minder, Iris Mashimo, Anna M Schläfli, Deborah Krauer, Elena A Federzoni, Bich Vu, James J Moresco, John R Yates and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. AdipocyteCells · 2026
    Article
  3. Article
  4. The moonlighting functions of glycolytic enzymes in tumorigenesis.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
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  6. 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

17 authors at 5 institutions in 3 countries.

Kristina SeilerDivision of Experimental Pathology, Institute of Pathology, University of Bern, Bern, Switzerland.
Magali HumbertDivision of Experimental Pathology, Institute of Pathology, University of Bern, Bern, Switzerland.ORCID 0000-0003-3820-0297
Petra MinderDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.
Iris MashimoDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.
Anna M SchläfliDivision of Experimental Pathology, Institute of Pathology, University of Bern, Bern, Switzerland.
Deborah KrauerDivision of Experimental Pathology, Institute of Pathology, University of Bern, Bern, Switzerland.
Elena A FederzoniDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.
Bich VuDepartment of Biology, University of Fribourg, Fribourg, Switzerland.
James J MorescoDepartment of Molecular Medicine, Scripps Research, La Jolla, CA, USA.ORCID 0000-0003-1178-1642
John R YatesDepartment of Molecular Medicine, Scripps Research, La Jolla, CA, USA.ORCID 0000-0001-5267-1672
Martin C SadowskiDivision of Experimental Pathology, Institute of Pathology, University of Bern, Bern, Switzerland.
Ramin RadpourDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID 0000-0002-5632-7833
Thomas KaufmannInstitute of Pharmacology, University of Bern, Bern, Switzerland.ORCID 0000-0001-9906-874X
Jean-Emmanuel SarryCentre de Recherches en Cancérologie de Toulouse, Université de Toulouse, Inserm, CNRS, Toulouse, France.ORCID 0000-0002-6704-2032
Joern DengjelDepartment of Biology, University of Fribourg, Fribourg, Switzerland.ORCID 0000-0002-9453-4614
Mario P TschanDivision of Experimental Pathology, Institute of Pathology, University of Bern, Bern, Switzerland. mario.tschan@pathology.unibe.ch.ORCID 0000-0001-5897-3647
Bruce E TorbettDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA. betorbet@uw.edu.ORCID 0000-0003-4995-1694
University of Bern · CHScripps Institution of Oceanography · USUniversity of Fribourg · CHCentre National de la Recherche Scientifique · FRScripps Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The family of hexokinases (HKs) catalyzes the first step of glycolysis, the ATP-dependent phosphorylation of glucose to glucose-6-phosphate. While HK1 and HK2 are ubiquitously expressed, the less well-studied HK3 is primarily expressed in hematopoietic cells and tissues and is highly upregulated during terminal differentiation of some acute myeloid leukemia (AML) cell line models. Here we show that expression of HK3 is predominantly originating from myeloid cells and that the upregulation of this glycolytic enzyme is not restricted to differentiation of leukemic cells but also occurs during ex vivo myeloid differentiation of healthy CD34

Indexed as

HexokinaseLeukemia, Myeloid, AcuteCell SurvivalGlycolysisHumansMyeloid CellsHexokinase

Identifiers

PMID35538058
PMCPMC9091226
OpenAlexW4280562070

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.