Evidence map›Paper›PMID 38153418›Full record

ArticleeLife2023

Iron chelation improves ineffective erythropoiesis and iron overload in myelodysplastic syndrome mice.

Wenbin An, Maria Feola, Maayan Levy, Srinivas Aluri, Marc Ruiz-Martinez, Ashwin Sridharan, Eitan Fibach, Xiaofan Zhu, Amit Verma, Yelena Ginzburg

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Macrophage ferroptosis in hematologic malignancies: emerging mechanisms and therapeutic implications.Apoptosis : an international journal on programmed cell death · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Iron-Loading Anemias.Advances in experimental medicine and biology · 2025
    Review
  12. 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

10 authors at 4 institutions in 4 countries.

Wenbin AnDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, United States.
Maria FeolaDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, United States.
Maayan LevyDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, United States.
Srinivas AluriDivision of Hematology and Medical Oncology, Albert Einstein College of Medicine, Bronx, United States.
Marc Ruiz-MartinezDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, United States.
Ashwin SridharanDivision of Hematology and Medical Oncology, Albert Einstein College of Medicine, Bronx, United States.
Eitan FibachDepartment of Hematology, Hadassah Medical Center, Hebrew University, Jerusalem, Israel.
Xiaofan ZhuState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Division of Pediatric Blood Diseases Center, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Amit VermaDivision of Hematology and Medical Oncology, Albert Einstein College of Medicine, Bronx, United States.ORCID 0000-0002-5408-1673
Yelena GinzburgDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, United States.ORCID 0000-0002-3496-3783
Cancer Institute (WIA) · INAlbert Einstein College of Medicine · USChinese Academy of Medical Sciences & Peking Union Medical College · CNHadassah Medical Center · IL

Funding

Chiesi USA ApoPharma Grant
6 · The paper itself

Abstract

Myelodysplastic syndrome (MDS) is a heterogeneous group of bone marrow stem cell disorders characterized by ineffective hematopoiesis and cytopenias, most commonly anemia. Red cell transfusion therapy for anemia in MDS results in iron overload, correlating with reduced overall survival. Whether the treatment of iron overload benefits MDS patients remains controversial. We evaluate underlying iron-related pathophysiology and the effect of iron chelation using deferiprone on erythropoiesis in NUP98-HOXD13 transgenic mice, a highly penetrant well-established MDS mouse model. Our results characterize an iron overload phenotype with aberrant erythropoiesis in these mice which was reversed by deferiprone-treatment. Serum erythropoietin levels decreased while erythroblast erythropoietin receptor expression increased in deferiprone-treated MDS mice. We demonstrate, for the first time, normalized expression of the iron chaperones

Indexed as

AnemiaIron OverloadAnimalsDeferiproneErythropoiesisFerritinsHumansIronIron Chelating AgentsMiceMice, TransgenicDeferiproneFerritinsIronIron Chelating Agentsdeferiproneineffective erythropoiesisiron traffickingmedicinemousemyelodysplastic dyndromeregenerative medicinestem cells

Identifiers

PMID38153418
PMCPMC10754500
OpenAlexW4390347893

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.