Evidence map›Paper›PMID 30630985›Full record

ArticleHaematologica2019

NCOA4 maintains murine erythropoiesis via cell autonomous and non-autonomous mechanisms.

Naiara Santana-Codina, Sebastian Gableske, Maria Quiles del Rey, Beata Małachowska, Mark P Jedrychowski, Douglas E Biancur, Paul J Schmidt, Mark D Fleming, Wojciech Fendler, J Wade Harper and 2 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 55 citations in OpenAlex.

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  12. Methods for Monitoring NCOA4-Mediated Ferritinophagy.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Molecular Mechanisms of Iron and Heme Metabolism.Annual review of nutrition · 2022
    Review
  18. The mutual crosstalk between iron and erythropoiesis.International journal of hematology · 2022
    Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 2 countries.

Naiara Santana-CodinaDivision of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Sebastian GableskeDivision of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Maria Quiles del ReyDivision of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Beata MałachowskaDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Poland.
Mark P JedrychowskiDivision of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Douglas E BiancurDivision of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Paul J SchmidtDepartment of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.
Mark D FlemingDepartment of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.
Wojciech FendlerDivision of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
J Wade HarperDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.
Alec C KimmelmanDepartment of Radiation Oncology, Perlmutter Cancer Center, New York University School of Medicine, New York, NY, USA.
Joseph D ManciasDivision of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA joseph_mancias@dfci.harvard.edu.
Dana-Farber Cancer Institute · USHarvard University · USBoston Children's Hospital · USMedical University of Lodz · PLMedical University of Warsaw · PLNew York University · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI JENNIFER W MACK · 1985 to 2026
$330.6M
Network organization of the human autophagy systemR01GM095567 · NIGMS · HARVARD MEDICAL SCHOOL · PI HARPER, JEFFREY W, KIMMELMAN, ALEC · 2011 to 2018
$3.0M
NCI NIH HHS P30 CA006516NIGMS NIH HHS R01 GM095567
6 · The paper itself

Abstract

Ncoa4 mediates autophagic degradation of ferritin, the cytosolic iron storage complex, to maintain intracellular iron homeostasis. Recent evidence also supports a role for Ncoa4 in systemic iron homeostasis and erythropoiesis. However, the specific contribution and temporal importance of Ncoa4-mediated ferritinophagy in regulating systemic iron homeostasis and erythropoiesis is unclear. Here, we show that Ncoa4 has a critical role in basal systemic iron homeostasis and both cell autonomous and non-autonomous roles in murine erythropoiesis. Using an inducible murine model of

Indexed as

ErythropoiesisHomeostasisAnemiaAnimalsAutophagyFemaleHemolysisHumansIronK562 CellsMaleMiceMice, Inbred C57BLMice, KnockoutNuclear Receptor CoactivatorsIronNcoA4 protein, mouseNuclear Receptor Coactivators

Identifiers

PMID30630985
PMCPMC6601094
OpenAlexW2909920511

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.