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Therapeutic potential of iron chelators in diseases associated with iron mismanagement

Identifieur interne : 001C43 ( Main/Exploration ); précédent : 001C42; suivant : 001C44

Therapeutic potential of iron chelators in diseases associated with iron mismanagement

Auteurs : Eugene D. Weinberg [États-Unis]

Source :

RBID : ISTEX:BA6151A3E8740DCD51C568F71DD18DA94A802450

English descriptors

Abstract

A considerable array of diseases are now recognized to be associated with misplacement of iron. Excessive deposits of the metal in sensitive tissue sites can result in formation of destructive hydroxyl radicals as well as in stimulation of growth of neoplastic and microbial cell invaders. To counteract potential iron damage, hosts employ the iron chelators, transferrin and lactoferrin. These proteins have been recently developed into pharmaceutical products. Additionally, a variety of low molecular mass iron chelators are being used/tested to treat whole body iron loading, and specific diseases for which the metal is a known or suspected risk factor.

Url:
DOI: 10.1211/jpp.58.5.0001


Affiliations:


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Le document en format XML

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<term>Antineoplastic action</term>
<term>Antineoplastic activity</term>
<term>Atherosclerotic lesions</term>
<term>Autoimmune encephalomyelitis</term>
<term>Bacterial adhesion</term>
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<term>Desferrioxamine</term>
<term>Dexrazoxane</term>
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<term>Fems immunol</term>
<term>Free iron</term>
<term>Free radic</term>
<term>Free radicals</term>
<term>Gallium nitrate</term>
<term>Haeme synthesis</term>
<term>Host cells</term>
<term>Host iron</term>
<term>Human lactoferrin</term>
<term>Human plasma</term>
<term>Hydroxyl radicals</term>
<term>Indiana university</term>
<term>Iron</term>
<term>Iron chelation</term>
<term>Iron chelation therapy</term>
<term>Iron chelator</term>
<term>Iron chelators</term>
<term>Iron deficiency</term>
<term>Iron depletion</term>
<term>Iron metabolism</term>
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<term>Iron saturation</term>
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<term>Isonicotinoyl</term>
<term>Isonicotinoyl hydrazone</term>
<term>Lactoferrin</term>
<term>Lipid peroxidation</term>
<term>Lupus erythematosus</term>
<term>Molecular mass iron chelators</term>
<term>Oral candidiasis suppression</term>
<term>Other iron chelators</term>
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<term>Pharmacol</term>
<term>Potential applications</term>
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<term>Transferrin</term>
<term>Transferrin saturation</term>
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<div type="abstract" xml:lang="en">A considerable array of diseases are now recognized to be associated with misplacement of iron. Excessive deposits of the metal in sensitive tissue sites can result in formation of destructive hydroxyl radicals as well as in stimulation of growth of neoplastic and microbial cell invaders. To counteract potential iron damage, hosts employ the iron chelators, transferrin and lactoferrin. These proteins have been recently developed into pharmaceutical products. Additionally, a variety of low molecular mass iron chelators are being used/tested to treat whole body iron loading, and specific diseases for which the metal is a known or suspected risk factor.</div>
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