Evidence map›Paper›PMID 23332666›Full record

ReviewCurrent opinion in chemical biology2013

Clawing back: broadening the notion of metal chelators in medicine.

Katherine J Franz

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in chemical biology, 2013. 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
4.4field-weighted citation impact, top 6% 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, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. CuChemical science · 2018
    Article
  8. Copper signalling: causes and consequences.Cell communication and signaling : CCS · 2018
    Review
  9. Article
  10. Developing drugs targeting transition metal homeostasis.Current opinion in chemical biology · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Sirtuin inhibitor sirtinol is an intracellular iron chelator.Chemical communications (Cambridge, England) · 2015
    Article
  17. Article
  18. 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

1 author at 1 institution in 1 country.

Katherine J FranzDepartment of Chemistry, Duke University, 124 Science Drive, Durham, NC 27708, USA. katherine.franz@duke.edu
Duke University · US

Funding

Metals, Drugs and Fungal PathogensR01GM084176 · NIGMS · DUKE UNIVERSITY · PI FRANZ, KATHERINE J. · 2008 to 2021
$4.3M
NIGMS NIH HHS GM084176NIGMS NIH HHS R01 GM084176
6 · The paper itself

Abstract

The traditional notion of chelation therapy is the administration of a chemical agent to remove metals from the body. But formation of a metal-chelate can have biological ramifications that are much broader than metal elimination. Exploring these other possibilities could lead to pharmacological interventions that alter the concentration, distribution, or reactivity of metals in targeted ways for therapeutic benefit. This review highlights recent examples that showcase four general strategies of using principles of metal chelation in medicinal contexts beyond the traditional notion of chelation therapy. These strategies include altering metal biodistribution, inhibiting specific metalloenzymes associated with disease, enhancing the reactivity of a metal complex to promote cytotoxicity, and conversely, passivating the reactivity of metals by site-activated chelation to prevent cytotoxicity.

Indexed as

AnimalsChelating AgentsChelation TherapyHumansMetalloproteinsTissue DistributionChelating AgentsMetalloproteins

Identifiers

PMID23332666
PMCPMC3634900
OpenAlexW2024587961

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.