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The IMP dehydrogenase inhibitor mycophenolic acid antagonizes the CTP synthetase inhibitor 3-deazauridine in MOLT-3 human leukemia cells: a central role for phosphoribosyl pyrophosphate.
- Source :
-
Biochemical pharmacology [Biochem Pharmacol] 1995 Sep 28; Vol. 50 (7), pp. 1095-8. - Publication Year :
- 1995
-
Abstract
- Mycophenolic acid, an inhibitor of the enzyme IMP dehydrogenase, antagonizes the CTP synthetase inhibitor 3-deazauridine in its anti-proliferative effects on MOLT-3 human T leukemia cells. No depletion of CTP occurred, and decreased amounts of 3-deazuridine-triphosphate were measured in cells incubated with mycophenolic acid and 3-deazuridine. Most probably, these phenomena are related to the increased amounts of PRPP observed, which can result in an increased pyrimidine biosynthesis de novo and, as a consequence, a decreased metabolism of 3-deazauridine via the salvage pathway.
- Subjects :
- 3-Deazauridine antagonists & inhibitors
Cell Division drug effects
Cell Survival drug effects
Dose-Response Relationship, Drug
Humans
Leukemia
Ribonucleotides biosynthesis
Tumor Cells, Cultured
3-Deazauridine pharmacology
Carbon-Nitrogen Ligases
Enzyme Inhibitors pharmacology
IMP Dehydrogenase antagonists & inhibitors
Ligases antagonists & inhibitors
Mycophenolic Acid pharmacology
Phosphoribosyl Pyrophosphate metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-2952
- Volume :
- 50
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Biochemical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 7575666
- Full Text :
- https://doi.org/10.1016/0006-2952(95)00228-r