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For many years iron chelators have been used for the treatment of iron overload disease and cancer. Nonetheless, the development of novel synthetic chelators with improved bioavaliability and reduced cytotoxicity remains an area of much interest. This thesis is an examination of some mechanisms through which iron binding agents cause toxicity. Two novel classes of iron chelator were compared to clinically relevant chelators with a range of cytotoxic profiles. A variety of assays were employed to categorise these agents in terms of their capacity to withdraw iron from cells, to generate oxygen…mehr

Produktbeschreibung
For many years iron chelators have been used for the
treatment of iron overload disease and cancer.
Nonetheless, the development of novel synthetic
chelators with improved bioavaliability and reduced
cytotoxicity remains an area of much interest. This
thesis is an examination of some mechanisms through
which iron binding agents cause toxicity. Two novel
classes of iron chelator were compared to clinically
relevant chelators with a range of cytotoxic
profiles. A variety of assays were employed to
categorise these agents in terms of their capacity to
withdraw iron from cells, to generate oxygen radicals
and to damage to DNA. In correlating these properties
with in vitro effects on proliferation it emerges
that toxicity of iron chelators arises from cellular
iron deprivation, the induction of oxidative stress
and biomolecular localisation of oxygen radicals.
In identifying functional structural elements and
iron binding motifs this work indicates biological
consequences to be considered in the design of iron
binding chemotherapeutic agents.
Autorenporträt
Timothy Chaston:
Timothy B. Chaston, B.AppSci, Ph.D.: Post Doctoral Research
Associate, Kings College London, London, UK.
Des Richardson:
Des R. Richardson, B.Sc., M.Sc., Ph.D., D.Sc: Professor of
Cancer Cell Biology, NHMRC Senior Principal Research Fellow,
Director of Iron Metabolism and Chelation Program, University of
Sydney, Sydney, Australia.