Evidence map›Paper›PMID 26669208›Full record

ReviewExpert review of hematology2016

Modulation of hepcidin to treat iron deregulation: potential clinical applications.

Nicole L Blanchette, David H Manz, Frank M Torti, Suzy V Torti

Abstract readReview
In one paragraph

Review in Expert review of hematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Iron and Cancer.Advances in experimental medicine and biology · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Iron as a Central Player and Promising Target in Cancer Progression.International journal of molecular sciences · 2019
    Review
  20. The interplay between iron and oxygen homeostasis with a particular focus on the heart.Journal of applied physiology (Bethesda, Md. : 1985) · 2017
    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 at 1 institution in 1 country.

Nicole L Blanchettea Department of Molecular Biology and Biophysics , University of Connecticut Health , Farmington , CT , USA.
David H Manza Department of Molecular Biology and Biophysics , University of Connecticut Health , Farmington , CT , USA.
Frank M Tortic Department of Medicine , University of Connecticut Health , Farmington , CT , USA.
Suzy V Tortia Department of Molecular Biology and Biophysics , University of Connecticut Health , Farmington , CT , USA.
UConn Health · US

Funding

Skeletal, Craniofacial and Oral Biology Training GrantT90DE021989 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MINA, MINA · 2011 to 2022
$4.5M
Iron, Ferroptosis and Ovarian CancerR01CA188025 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI TORTI, SUZY V · 2014 to 2024
$3.9M
Ferroportin and Iron HomeostasisR01CA171101 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI TORTI, FRANK M. · 2012 to 2016
$1.7M
Skeletal, Craniofacial and Oral Biology Training GrantR90DE022526 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MINA, MINA · 2011 to 2022
$627k
NCI NIH HHS R01 CA171101NCI NIH HHS R01 CA188025NIDCR NIH HHS R90 DE022526NIDCR NIH HHS T90 DE021989
6 · The paper itself

Abstract

The secreted peptide hormone hepcidin regulates systemic and local iron homeostasis through degradation of the iron exporter ferroportin. Dysregulation of hepcidin leads to altered iron homeostasis and development of pathological disorders including hemochromatosis, and iron loading and iron restrictive anemias. Therapeutic modulation of hepcidin is a promising method to ameliorate these conditions. Several approaches have been taken to enhance or reduce the effects of hepcidin in vitro and in vivo. Based on these approaches, hepcidin modulating drugs have been developed and are undergoing clinical evaluation. In this article we review the rationale for development of these drugs, the data concerning their safety and efficacy, their therapeutic uses, and potential future prospects.

Indexed as

AnimalsBiological TransportBone Morphogenetic Protein ReceptorsBone Morphogenetic ProteinsCation Transport ProteinsFerroportinGene Expression RegulationHepcidinsHomeostasisHumansInterleukin-6IronIron Metabolism DisordersPeptide HormonesSignal TransductionBone Morphogenetic Protein ReceptorsBone Morphogenetic ProteinsCation Transport ProteinsErfe protein, humanFerroportinHepcidinsInterleukin-6IronPeptide Hormonesanemia of chronic diseaseclinical trialsferroportinHepcidiniron deficiencyiron overload

Identifiers

PMID26669208
PMCPMC4849272
OpenAlexW2220192676

What OpenQuestion holds

Textmetadata
LicenceTDM
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.