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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
25
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pubmed:dateCreated |
2003-12-3
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pubmed:abstractText |
The current study demonstrates unequivocally that polyamines can serve as vectors for the intracellular delivery of the bidentate chelator 1,2-dimethyl-3-hydroxypyridin-4-one (L1). The polyamine-hydroxypyridinone conjugate 1-(12-amino-4,9-diazadodecyl)-2-methyl-3-hydroxy-4(1H)-pyridinone is assembled from spermine and 3-O-benzylmaltol. The conjugate is shown to form a 3:1 complex with Fe(III) and to be taken up by the polyamine transporter 1900-fold against a concentration gradient. The K(i) of the conjugate is 3.7 microM vs spermidine for the polyamine transporter. The conjugate is also at least 230 times more active in suppressing the growth of L1210 murine leukemia cells than is the parent ligand, decreases the activities of the polyamine biosynthetic enzymes ornithine decarboxylase and S-adenosylmethionine decarboxylase, and upregulates spermidine-spermine N (1)-acetyltransferase. However, the effect on native polyamine pools is a moderate one. These findings are in keeping with the idea that polyamines can also serve as efficient vectors for the intracellular delivery of other iron chelators.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetyltransferases,
http://linkedlifedata.com/resource/pubmed/chemical/Adenosylmethionine Decarboxylase,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Ferric Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Iron Chelating Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Ornithine Decarboxylase,
http://linkedlifedata.com/resource/pubmed/chemical/Polyamines,
http://linkedlifedata.com/resource/pubmed/chemical/Pyridones,
http://linkedlifedata.com/resource/pubmed/chemical/Spermine,
http://linkedlifedata.com/resource/pubmed/chemical/diamine N-acetyltransferase
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-2623
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
4
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pubmed:volume |
46
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5478-83
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:14640556-Acetyltransferases,
pubmed-meshheading:14640556-Adenosylmethionine Decarboxylase,
pubmed-meshheading:14640556-Animals,
pubmed-meshheading:14640556-Antineoplastic Agents,
pubmed-meshheading:14640556-Binding, Competitive,
pubmed-meshheading:14640556-Biological Transport, Active,
pubmed-meshheading:14640556-Carrier Proteins,
pubmed-meshheading:14640556-Cell Division,
pubmed-meshheading:14640556-Cell Line, Tumor,
pubmed-meshheading:14640556-Drug Screening Assays, Antitumor,
pubmed-meshheading:14640556-Ferric Compounds,
pubmed-meshheading:14640556-Iron Chelating Agents,
pubmed-meshheading:14640556-Leukemia L1210,
pubmed-meshheading:14640556-Mice,
pubmed-meshheading:14640556-Ornithine Decarboxylase,
pubmed-meshheading:14640556-Polyamines,
pubmed-meshheading:14640556-Pyridones,
pubmed-meshheading:14640556-Spermine,
pubmed-meshheading:14640556-Up-Regulation
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pubmed:year |
2003
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pubmed:articleTitle |
Polyamine-iron chelator conjugate.
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pubmed:affiliation |
Department of Medicinal Chemistry, University of Florida, Gainesville, Florida 32610-0485, USA. bergeron@mc.cop.ufl.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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