Evidence map›Paper›PMID 29209212›Full record

ArticleFrontiers in pharmacology2017

Identification of Antibody and Small Molecule Antagonists of Ferroportin-Hepcidin Interaction.

Sandra L Ross, Kaustav Biswas, James Rottman, Jennifer R Allen, Jason Long, Les P Miranda, Aaron Winters, Tara L Arvedson

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. mBio · 2026
    Article
  3. Discovery of Therapeutic Antibodies Targeting Complex Multi-Spanning Membrane Proteins.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Therapeutic Advances in Regulating the Hepcidin/Ferroportin Axis.Pharmaceuticals (Basel, Switzerland) · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Iron as a Therapeutic Target inPharmaceuticals (Basel, Switzerland) · 2018
    Review
  18. Hepcidin Therapeutics.Pharmaceuticals (Basel, Switzerland) · 2018
    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

8 authors at 1 institution in 1 country.

Sandra L RossDepartment of Oncology Research, Amgen Inc., Thousand Oaks, CA, United States.
Kaustav BiswasDepartment of Hybrid Modality Engineering, Amgen Inc., Thousand Oaks, CA, United States.
James RottmanDepartment of Comparative Biology and Safety Sciences, Amgen Inc., Thousand Oaks, CA, United States.
Jennifer R AllenDepartment of Medicinal Chemistry, Amgen Inc., Thousand Oaks, CA, United States.
Jason LongDepartment of Hybrid Modality Engineering, Amgen Inc., Thousand Oaks, CA, United States.
Les P MirandaDepartment of Hybrid Modality Engineering, Amgen Inc., Thousand Oaks, CA, United States.
Aaron WintersDepartment of Therapeutic Discovery, Amgen Inc., Thousand Oaks, CA, United States.
Tara L ArvedsonDepartment of Oncology Research, Amgen Inc., Thousand Oaks, CA, United States.
Amgen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The iron exporter ferroportin and its ligand, the hormone hepcidin, control fluxes of stored and recycled iron for use in a variety of essential biochemical processes. Inflammatory disorders and malignancies are often associated with high hepcidin levels, leading to ferroportin down-regulation, iron sequestration in tissue macrophages and subsequent anemia. The objective of this research was to develop reagents to characterize the expression of ferroportin, the interaction between ferroportin and hepcidin, as well as to identify novel ferroportin antagonists capable of maintaining iron export in the presence of hepcidin. Development of investigative tools that enabled cell-based screening assays is described in detail, including specific and sensitive monoclonal antibodies that detect endogenously-expressed human and mouse ferroportin and fluorescently-labeled chemically-synthesized human hepcidin. Large and small molecule antagonists inhibiting hepcidin-mediated ferroportin internalization were identified, and unique insights into the requirements for interaction between these two key iron homeostasis molecules are provided.

Indexed as

antibody engineeringanti-ferroportin monoclonal antibodyferroportinferroportin antagonistfluorescently-labeled hepcidinhepcidiniron metabolismreceptor internalization

Identifiers

PMID29209212
PMCPMC5702341
OpenAlexW2769664694

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.