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Gallium and its competing roles with iron in biological systems.

Abstract
Gallium, a group IIIa metal, shares chemical properties with iron. Studies have shown that gallium-based compounds have potential therapeutic activity against certain cancers and infectious microorganisms. By functioning as an iron mimetic, gallium perturbs iron-dependent proliferation processes in tumor cells. Gallium's action on iron homeostasis leads to disruption of ribonucleotide reductase, mitochondrial function, and the regulation of transferrin receptor and ferritin. In addition, gallium nitrate stimulates an increase in mitochondrial reactive oxygen species in cells which triggers downstream upregulation of metallothionein and hemoxygenase-1. Gallium's anti-infective activity against bacteria and fungi results from disruption of microbial iron utilization through mechanisms which include gallium binding to siderophores and downregulation of bacterial iron uptake. Gallium compounds lack cross-resistance to conventional chemotherapeutic drugs and antibiotics thus making them attractive agents for drug development. This review will focus on the mechanisms of action of gallium with emphasis on its interaction with iron and iron proteins.
AuthorsChristopher R Chitambar
JournalBiochimica et biophysica acta (Biochim Biophys Acta) Vol. 1863 Issue 8 Pg. 2044-53 (08 2016) ISSN: 0006-3002 [Print] Netherlands
PMID27150508 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
CopyrightCopyright © 2016 Elsevier B.V. All rights reserved.
Chemical References
  • Anti-Infective Agents
  • Antineoplastic Agents
  • Gallium Isotopes
  • Nonheme Iron Proteins
  • Transferrin
  • Gallium
  • Iron
  • gallium nitrate
Topics
  • Animals
  • Anti-Infective Agents (pharmacology)
  • Antineoplastic Agents (pharmacology)
  • Biological Transport
  • Drug Evaluation
  • Drug Screening Assays, Antitumor
  • Gallium (pharmacokinetics, pharmacology, therapeutic use)
  • Gallium Isotopes (analysis, pharmacokinetics, therapeutic use)
  • Homeostasis
  • Humans
  • Iron (physiology)
  • Mice
  • Mitochondria (drug effects)
  • Neoplasms (metabolism)
  • Nonheme Iron Proteins (metabolism)
  • Rats
  • Transferrin (metabolism)

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