Evidence map›Paper›PMID 37578340›Full record

ArticleeLife2023

Normal and dysregulated crosstalk between iron metabolism and erythropoiesis.

Yelena Ginzburg, Xiuli An, Stefano Rivella, Adam Goldfarb

Abstract 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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Trial
  2. Mechanisms of Thrombocytosis in Iron-Deficiency Anemia.European journal of haematology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Macrophage ferroptosis in hematologic malignancies: emerging mechanisms and therapeutic implications.Apoptosis : an international journal on programmed cell death · 2026
    Review
  8. Heme-mediated selection of encapsulatedEmerging microbes & infections · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Daily iron supplementation for prevention or treatment of moderate iron deficiency anemia in patients with solid neoplasm, undergoing concurrent radiochemotherapy treatment.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2025
    Review
  19. Diagnostics: Markers of Body Iron Status.Advances in experimental medicine and biology · 2025
    Review
  20. 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

4 authors.

Yelena GinzburgDivision of Hematology and Medical Oncology, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, United States.ORCID https://orcid.org/0000-0002-3496-3783
Xiuli AnLFKRI, New York Blood Center, New York, United States.
Stefano RivellaDepartment of Pediatrics, Division of Hematology, The Children's Hospital of Philadelphia, Philadelphia, United States.
Adam GoldfarbDepartment of Pathology, University of Virginia, Charlottesville, United States.

Funding

Sickle cell bone marrow niche and regulation of platelet activation and erythropoiesisP01HL149626 · NHLBI · NEW YORK BLOOD CENTER · PI Karina Yazdanbakhsh · 2020 to 2026
$24.4M
Regulatory Role of Transferrin in Erythropoiesis and Iron MetabolismR01DK095112 · NIDDK · SAINT LOUIS UNIVERSITY · PI Robert E Fleming, Yelena Ginzburg · 2012 to 2026
$5.4M
Iron Deficiency: Molecular and Cellular ConsequencesR01DK079924 · NIDDK · UNIVERSITY OF VIRGINIA · PI GOLDFARB, ADAM N. · 2008 to 2023
$5.2M
The Role of Erythroferrone in Regulating Bone Metabolism in Beta-ThalassemiaR01DK107670 · NIDDK · NEW YORK BLOOD CENTER · PI GINZBURG, YELENA, YUEN, TONY · 2015 to 2025
$4.5M
Transfusion-driven hyperhemolysis in sickle cell diseaseR01HL165202 · NHLBI · NEW YORK BLOOD CENTER · PI Xiuli An, HUI ZHONG · 2023 to 2026
$3.2M
Use of forward Genetic approaches to identify Babesia receptorsR01HL140625 · NHLBI · NEW YORK BLOOD CENTER · PI AN, XIULI, LOBO, CHERYL ANN · 2018 to 2021
$2.8M
Development and validation of novel mouse models and expression vectors for characterizing severe alpha-thalassemia pathophysiology and evaluating gene therapy approaches.R01DK133475 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI STEFANO RIVELLA · 2023 to 2026
$2.5M
Transfusion-driven hyperhemolysis in sickle cell diseaseR56HL165202 · NHLBI · NEW YORK BLOOD CENTER · PI AN, XIULI, ZHONG, HUI · 2022 to 2022
$804k
Validation of Aconitase-Isocitrate Pathway as a Target for Anemia TreatmentR01DK101550 · NIDDK · UNIVERSITY OF VIRGINIA · PI GOLDFARB, ADAM N. · 2016 to 2018
$711k
Mechanistic understanding of dysregulated iron metabolism in polycythemia veraR56DK132146 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GINZBURG, YELENA, HOFFMAN, RONALD · 2022 to 2022
$100k
NHLBI NIH HHS P01 HL149626NHLBI NIH HHS R01 HL140625NHLBI NIH HHS R01 HL165202NHLBI NIH HHS R56 HL165202NIDDK NIH HHS R01 DK079924NIDDK NIH HHS R01 DK095112NIDDK NIH HHS R01 DK101550NIDDK NIH HHS R01 DK107670NIDDK NIH HHS R01 DK133475NIDDK NIH HHS R56 DK132146NIH HHS DK079924NIH HHS DK095112NIH HHS DK101550NIH HHS DK107670NIH HHS DK132146NIH HHS DK133475NIH HHS HL140625NIH HHS HL149626NIH HHS HL165202
6 · The paper itself

Abstract

Erythroblasts possess unique characteristics as they undergo differentiation from hematopoietic stem cells. During terminal erythropoiesis, these cells incorporate large amounts of iron in order to generate hemoglobin and ultimately undergo enucleation to become mature red blood cells, ultimately delivering oxygen in the circulation. Thus, erythropoiesis is a finely tuned, multifaceted process requiring numerous properly timed physiological events to maintain efficient production of 2 million red blood cells per second in steady state. Iron is required for normal functioning in all human cells, the erythropoietic compartment consuming the majority in light of the high iron requirements for hemoglobin synthesis. Recent evidence regarding the crosstalk between erythropoiesis and iron metabolism sheds light on the regulation of iron availability by erythroblasts and the consequences of insufficient as well as excess iron on erythroid lineage proliferation and differentiation. In addition, significant progress has been made in our understanding of dysregulated iron metabolism in various congenital and acquired malignant and non-malignant diseases. Finally, we report several actual as well as theoretical opportunities for translating the recently acquired robust mechanistic understanding of iron metabolism regulation to improve management of patients with disordered erythropoiesis, such as anemia of chronic inflammation, β-thalassemia, polycythemia vera, and myelodysplastic syndromes.

Indexed as

beta-ThalassemiaErythropoiesisErythrocytesHemoglobinsHumansIronHemoglobinsIronanemiadevelopmental biologyerythropoiesisiron deficiencymedicinepolycythemia

Identifiers

PMID37578340
PMCPMC10425177

What Socratic 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 Socratic graph.