Evidence map›Paper›PMID 37487020›Full record

ArticleBlood advances2023

Ciclopirox ethanolamine preserves the immature state of human HSCs by mediating intracellular iron content.

Mehrnaz Safaee Talkhoncheh, Aurélie Baudet, Fredrik Ek, Agatheeswaran Subramaniam, Yun-Ruei Kao, Natsumi Miharada, Christine Karlsson, Leal Oburoglu, Anna Rydström, Kristijonas Zemaitis and 6 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

16 authors at 2 institutions in 2 countries.

Mehrnaz Safaee TalkhonchehMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0001-8429-7566
Aurélie BaudetMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0002-3246-1819
Fredrik EkChemical Biology and Therapeutics, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Agatheeswaran SubramaniamMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0003-3966-3875
Yun-Ruei KaoDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.
Natsumi MiharadaMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.
Christine KarlssonMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.
Leal OburogluMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0003-0130-6602
Anna RydströmMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0002-3404-7195
Kristijonas ZemaitisMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0002-4098-0184
Abdul Ghani AlattarMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0002-0319-4416
Justyna RakMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.
Kristian PietrasDivision of Translational Cancer Research, Medicon Village, Lund University, Lund, Sweden.ORCID 0000-0001-6738-4705
Roger OlssonChemical Biology and Therapeutics, Department of Experimental Medical Science, Lund University, Lund, Sweden.ORCID 0000-0002-7107-3472
Britta WillDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.ORCID 0000-0002-9534-6690
Jonas LarssonMolecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund, Sweden.
Lund University · SEAlbert Einstein College of Medicine · US

Funding

Identification and targeting of pathways separating healthy stem cell aging from malignant transformationR01CA230756 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Britta Will · 2018 to 2026
$4.0M
NCI NIH HHS R01 CA230756
6 · The paper itself

Abstract

Culture conditions in which hematopoietic stem cells (HSCs) can be expanded for clinical benefit are highly sought after. To elucidate regulatory mechanisms governing the maintenance and propagation of human HSCs ex vivo, we screened libraries of annotated small molecules in human cord blood cells using an optimized assay for detection of functional HSCs during culture. We found that the antifungal agent ciclopirox ethanolamine (CPX) selectively supported immature CD34+CD90+ cells during culture and enhanced their long-term in vivo repopulation capacity. Purified HSCs treated with CPX showed a reduced cell division rate and an enrichment of HSC-specific gene expression patterns. Mechanistically, we found that the HSC stimulating effect of CPX was directly mediated by chelation of the intracellular iron pool, which in turn affected iron-dependent proteins and enzymes mediating cellular metabolism and respiration. Our findings unveil a significant impact of iron homeostasis in regulation of human HSCs, with important implications for both basic HSC biology and clinical hematology.

Indexed as

Hematopoietic Stem CellsIronAntigens, CD34CiclopiroxEthanolaminesHumansAntigens, CD34CiclopiroxEthanolaminesIron

Identifiers

PMID37487020
PMCPMC10758717
OpenAlexW4385191229

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.