Future of toxicology--iron chelators and differing modes of action and toxicity: the changing face of iron chelation therapy.

Abstract:

:Iron (Fe) chelation therapy was initially designed to alleviate the toxic effects of excess Fe evident in Fe-overload diseases. However, the novel toxicological properties of some Fe chelator-metal complexes have shifted appreciable focus to their application in cancer chemotherapy. Redox-inactive Fe chelator complexes are well suited for the treatment of Fe-overload diseases, whereas Fe chelator complexes with high redox activity have shown promising results as chemotherapeutics against cancer. Within this perspective, we discuss the different modes of action and toxicological profiles of Fe chelators, including analogues of 2-pyridylcarboxaldehyde isonicotinoyl hydrazone, di-2-pyridylketone isonicotinoyl hydrazone, di-2-pyridylketone thiosemicarbazone, and the clinically trialed chelator 3-aminopyridine-2-carboxaldehyde thiosemicarbazone. The potential application of these agents in the changing face of Fe chelation therapy is discussed.

journal_name

Chem Res Toxicol

authors

Kalinowski DS,Richardson DR

doi

10.1021/tx700039c

subject

Has Abstract

pub_date

2007-05-01 00:00:00

pages

715-20

issue

5

eissn

0893-228X

issn

1520-5010

journal_volume

20

pub_type

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