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PMID: 7598507 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Polyamines as targets for therapeutic intervention.

Annual review of pharmacology and toxicology ·Vol. 35 ·1995-00-00 ·Pages 55-91

Marton LJ, Pegg AE

Abstract

Polyamines are ubiquitous cell components essential for normal growth. Compounds interfering with polyamine biosynthesis or function have considerable potential for use as therapeutic agents. Inhibitors of ornithine decarboxylase have been shown to be valuable for the treatment of diseases caused by parasitic protozoa, most notably African sleeping sickness. They may also be useful chemopreventive and antineoplastic agents. Inhibitors of S-adenosylmethionine decarboxylase also have potential as treatments of these diseases. Protocols minimizing uptake of exogenous polyamines via the polyamine-transport system will probably be needed for the full potential of the inhibitors to be realized. Polyamine analogues, notably those with ethyl or benzyl groups on the terminal nitrogen atoms, have potent antiproliferative activity and are promising agents for the treatment of cancer. These analogues are transported by the polyamine-transport system, and their therapeutic effects are less likely to be blocked by the availability of the exogenous polyamines.

MeSH Terms
Adenosylmethionine Decarboxylase/antagonists & inhibitors Biological Transport Combined Modality Therapy DNA/drug effects Eflornithine/therapeutic use Forecasting Humans Neoplasms/drug therapy,therapy Oncogenes Ornithine Decarboxylase/genetics Ornithine Decarboxylase Inhibitors Parasitic Diseases/drug therapy Polyamines/antagonists & inhibitors,metabolism
Chemicals
Ornithine Decarboxylase Inhibitors Polyamines DNA Ornithine Decarboxylase Adenosylmethionine Decarboxylase Eflornithine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Marton L J
Department of Pathology, University of Wisconsin Medical School, Madison 53706, USA.
Pegg A E
Article Info
Journal
Annual review of pharmacology and toxicology
Abbr.
Annu Rev Pharmacol Toxicol
ISSN
0362-1642
Published
1995-00-00
Pages
55-91
Language
English
Region
United States
NLM ID
7607088
Subset
IM
Grants
NCI NIH HHS · CA-13525 · United States
NCI NIH HHS · CA-18138 · United States
NIGMS NIH HHS · GM-26290 · United States
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