Purine nucleosides as cell-specific modulators of 5-fluorouracil metabolism and cytotoxicity
Purine nucleosides and ribose- 5-phosphate (Rib- 5-P) were used to modulate the metabolism and cytotoxicity of 5-fluorouracil ( 5-FU) in order to get better understanding of the mechanism of action of 5-FU. In extracts from five different cell lines both Rib- 5-P and inosine were relatively good pre...
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Veröffentlicht in: | European journal of cancer & clinical oncology 1987-12, Vol.23 (12), p.1869-1881 |
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Zusammenfassung: | Purine nucleosides and ribose-
5-phosphate (Rib-
5-P) were used to modulate the metabolism and cytotoxicity of
5-fluorouracil (
5-FU) in order to get better understanding of the mechanism of action of
5-FU. In extracts from five different cell lines both Rib-
5-P and inosine were relatively good precursors for Rib-
1-P, but deoxyinosine was a moderate to poor precursor for deoxyRib-
1-P. In the human colon carcinoma WiDr and the human epithelial intestinal Intestine
407 inosine enhanced Rib-
1-P concentrations
3–6-fold. Incubation with deoxyinosine resulted in the appearance of deoxyRib-
1-P in both cell lines in levels comparable to those of Rib-
1-P. dIMP had the same effect as deoxyinosine in Intestine
407 cells, but not in WiDr cells. Both inosine and deoxyinosine caused a depletion of phosphoribosyl-pyrophosphate.
In WiDr cells deoxyinosine
(0.1–1.0 mM) clearly potentiated the growth inhibition by
0.1–0.5 μM 5-FU after
24 h of culture, but growth between
24 and
48 h was normal. In Intestine
407 cells the potentiation of
5-FU cytotoxicity by deoxyinosine was even more pronounced at
48 h than at
24 h. In WiDr cells dIMP did not potentiate
5-FU cytotoxity, but in Intestine
407 cells the effect was comparable to that of deoxyinosine. The lack of potentiation in WiDr was accompanied by a low metabolism of dIMP. Growth inhibition by
5-FU and deoxyinosine could be reversed by thymidine in Intestine
407 cells but not completely in WiDr cells. Since the predominant target of the deoxyinosine-
5-FU combination was thymidylate synthase, we analyzed the inhibition of this enzyme by FdUMP and the retention of the inhibition in cell culture. In both cell lines FdUMP was a potent competitive inhibitor of thymidylate synthase with a
K
i
of between
0.5 and
2 nM. Culture of cells in the presence of
5-FU and deoxyinosine resulted in an almost complete inhibition of thymidylate synthase activity after
24 h but after
48 h the activity was partly recovered. In Intestine
407 cells replenishment of the culture medium at
24 h even enhanced the recovery. Analysis of
5-FU anabolism into nucleic acids demonstrated that deoxyinosine inhibited the incorporation of
5-FU into RNA. It is concluded that in Intestine
407 cells addition of deoxyinosine enhanced the effects of
5-FU on growth inhibition due to increased formation of FdUMP leading to enhanced inhibition of thymidylate synthase. In WiDr cells incorporation of
5-FU into RNA might also contribute significantly to cytotoxicity |
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ISSN: | 0277-5379 |
DOI: | 10.1016/0277-5379(87)90053-8 |