Inhibition of IMP Dehydrogenase by Mycophenolic Acid in Molt F4 Human Malignant Lymphoblasts

Author:

Stet Elisabet H1,De Abreu Ronney A1,Bökkerink Jos P M1,Lambooy Lambert H J1,Vogels-Mentink Trade M1,Keizer-Garritsen Jenneke J1,Trijbels Frans J M1

Affiliation:

1. SE Netherlands Centre for Paediatric Oncology, Department of Paediatrics, St Radboud University Hospital of Nijmegen, PO Box 9101, 6500 HB Nijmegen, The Netherlands

Abstract

The effects of inhibition of inosine monophosphate dehydrogenase (IMPDH), the rate-limiting enzyme in guanine nucleotide de novo synthesis, on cell growth, cell viability, endogenous nucleotide concentrations and concentrations of extracellular nucleosides and bases were studied in Molt F4 human malignant lymphoblasts. Mycophenolic acid (MPA) was used as a specific inhibitor of the enzyme activity. IMPDH activity was maximally inhibited with 0–5 μM MPA. After a 2 h exposure of the cells to 0–5 μM MPA, guanine nucleotides were depleted to approximately 50% of control values, whereas 5-phosphoribosyl-1-pyrophosphate levels increased to approximately 200%. Under these conditions, cytotoxicity became obvious after 24 h. Depletion of guanine nucleotides and cytotoxicity were prevented by addition of guanosine to MPA treatment. Daily supplements of guanosine were required to prevent MPA cytotoxicity during the entire incubation period of 72 h. We conclude that depletion of guanine nucleotides, induced by treatment with MPA, induces a severe and rapid cytotoxicity in Molt F4 cells.

Publisher

SAGE Publications

Subject

Clinical Biochemistry,General Medicine

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