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PMID: 12572997 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Therapeutic potential of iron chelators in cancer therapy.

Advances in experimental medicine and biology ·Vol. 509 ·2002-00-00 ·Pages 231-49

Richardson DR

Abstract

The success of DFO at markedly inhibiting the growth of aggressive tumors such as neuroblastoma and leukemia justifies interest in the development of chelators as anti-neoplastic agents. This is emphasized by the fact that DFO has suboptimal properties, namely poor membrane permeability and a very short serum half-life. More recently, the thiosemicarbazone chelator, Triapine, has entered a phase I clinical trial again confirming the potential of these compounds. Further studies examining the effects of chelators on neoplastic cells will not only be valuable in terms of identifing novel anti-cancer agents, but will also provide new information on the role of Fe in cell cycle control.

MeSH Terms
Animals Antineoplastic Agents/therapeutic use Cell Cycle/drug effects Deferoxamine/therapeutic use Humans Iron/metabolism Iron Chelating Agents/therapeutic use Isoniazid/analogs & derivatives,therapeutic use Neoplasms/drug therapy,metabolism,pathology Pyridoxal/analogs & derivatives,therapeutic use Thiosemicarbazones/therapeutic use Tumor Suppressor Protein p53/metabolism
Chemicals
Antineoplastic Agents Iron Chelating Agents Thiosemicarbazones Tumor Suppressor Protein p53 Pyridoxal pyridoxal isonicotinoyl hydrazone Iron Deferoxamine Isoniazid
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Richardson Des R
The Iron Metabolism and Chelation Group, The Heart Research Institute, 145 Missenden Rd, Camperdown, Sydney, New South Wales, 2050 Australia.
Article Info
Journal
Advances in experimental medicine and biology
Abbr.
Adv Exp Med Biol
ISSN
0065-2598
Published
2002-00-00
Pages
231-49
Language
English
Region
United States
NLM ID
0121103
Subset
IM
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