Abstract
Telomerase is thought to play an important role in the mechanism of tumor cell immortalization by maintenance of telomere length. To obtain information on the susceptibility of telomerase to nucleoside analogues, the effects of base-modified 3'-azido-2',3'-dideoxynucleoside triphosphates on the enzyme were investigated. It is suggested that the 2-amino group of the nucleotide purine nucleus is important for the inhibitory activity. Telomere shortening caused by long-term treatment with these nucleosides is also described.
MeSH terms
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Dideoxyadenosine / analogs & derivatives
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Dideoxyadenosine / chemistry
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Dideoxyadenosine / pharmacology
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Dideoxynucleosides / chemistry
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Dideoxynucleosides / pharmacology*
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Dideoxynucleotides / chemistry
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Dideoxynucleotides / pharmacology*
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Drug Design
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology
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HL-60 Cells
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Humans
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Telomerase / antagonists & inhibitors*
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Telomere / drug effects*
Substances
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Dideoxynucleosides
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Dideoxynucleotides
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Enzyme Inhibitors
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3'-azido-2,6-diaminopurine-2',3'-dideoxyriboside
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Dideoxyadenosine
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Telomerase