Lack of enhanced cytotoxicity of cultured L1210 cells using folinic acid in combination with sequential methotrexate and fluorouracil |
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Authors: | Lynn L Danhauser Robert Heimer Ed Cadman |
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Institution: | (1) Department of Medicine, Yale University School of Medicine, 06510 New Haven, CT, USA;(2) Department of Pharmacology, Yale University School of Medicine, 06510 New Haven, CT, USA;(3) Present address: Cancer Research Institute, University of California, M-1282, 94143 San Francisco, CA, USA |
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Abstract: | Summary Previous studies from this laboratory have demonstrated that treatment of cultured cells with sequential methotrexate (MTX) and fluorouracil (FUra) leads to synergistic cell killing in several murine and human neoplasms in vitro. In this study leucovorin (folinic acid, LCV) was added to the MTX/FUra combination with the intention of generating elevated levels of methylenetetrahydrofolate to promote the formation of a stable fluorodeoxyuridylate-thymidylate synthetase ternary complex, thereby augmenting the cytotoxicity of the MTX-FUra sequence. The addition of 10 or 100 M LCV concurrently with or after 10 M FUra following MTX (1 M) pretreatment did not augment the inhibition of L1210 cell growth or the clonigenicity compared with MTX prior to FUra without LCV. The effects of LCV schedulling on the sequential MTX and FUra-induced inhibition of thymidylate synthesis were measured by examining the rate of 6-3H] dUrd incorporation into the acid-precipitable cell fraction and by direct quantitation of the thymidylate synthetase ternary complex. Combination of 100 M LCV with 10 M FUra after 1 M MTX resulted in significantly more ternary complex formation than did 1 M MTX before 10 M FUra alone. The inhibitory effects of FUra on thymidylate synthetase in the presence of MTX, however, could not be augmented by LCV as determined by 6-3H] incorporation into acid-precipitable material, nor did the addition of LCV result in increased cytotoxicity. Factors other than the inhibition of DNA synthesis may be critical to the cytotoxicity of sequential MTX and FUra in L1210 cells.Abbreviations MTX
methotrexate
- FUra
5-fluorouracil
- LCV
d, 1-N
5-formyltetrahydrofolic acid, calcium salt (folinic acid, leucovorin)
- F dUMP
5-fluoro-2 -deoxyuridylate
- FUTP
5-fluorouidine-5-triphosphate
- PRPP
5-phosphoribosyl-1-pyrophosphate
- CH2FAH4
N
5,10-methylenetetrahydrofolate
- dUMP
2 -deoxyuridylate
- dTMP
thymidylate
- TS
thymidylate synthetase
- PBS
phosphate-buffered saline
- NaCl
8.0 g
- KCl
0.2 g
- Na2HPO4
1.15 g
- KH2PO4
0.2 g in 1 1 H2O, pH 7.4
- FdUrd
5-fluoro-2 -deoxyuridine
This work was supported in part by grant CH-145 from the American Cancer Society and by grants CA-27130 and CA-08341 from the National Cancer Institute. LLD was supported by Postdoctoral Training Grant S-T32-CA09085-08 from the National Institutes of Health and EC was the recipient of a Cancer Research Award from the American Cancer Society |
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