Use of electroporation to study the cytotoxic effects of fluorodeoxyuridylate in intact cells

The introduction of 2'-deoxyuridine 5'-monophosphate and its analog, 5-fluoro-2'-deoxyuridine 5'-monophosphate, into intact CCRF-CEM and NIH3T3 cells was achieved by electroporation. Following electroporation, cells were shown to be fully functional as monitored by the incorporat...

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Veröffentlicht in:Biochemical pharmacology 1987-04, Vol.36 (8), p.1345-1348
Hauptverfasser: Jastreboff, Margaret M., Sokoloski, John A., Bertino, Joseph R., Narayanan, Ramaswamy
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container_end_page 1348
container_issue 8
container_start_page 1345
container_title Biochemical pharmacology
container_volume 36
creator Jastreboff, Margaret M.
Sokoloski, John A.
Bertino, Joseph R.
Narayanan, Ramaswamy
description The introduction of 2'-deoxyuridine 5'-monophosphate and its analog, 5-fluoro-2'-deoxyuridine 5'-monophosphate, into intact CCRF-CEM and NIH3T3 cells was achieved by electroporation. Following electroporation, cells were shown to be fully functional as monitored by the incorporation of deoxyuridylate, after conversion to thymidylate, into DNA. Pretreatment of cells with fluorodeoxyuridine completely abolished this effect. In contrast, introduction of the fluoro analog into cells by electroporation markedly inhibited both DNA synthesis and cell growth in a time-dependent manner. Thus, electroporation offers a powerful tool to permeabilize cells to a variety of cellular metabolites and antimetabolites.
doi_str_mv 10.1016/0006-2952(87)90092-X
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subjects Cell Line
Cell Membrane Permeability
Cell Survival - drug effects
Deoxyuracil Nucleotides - pharmacology
Deoxyuridine - metabolism
DNA - metabolism
Fluorodeoxyuridylate - metabolism
Fluorodeoxyuridylate - pharmacology
Thymidylate Synthase - antagonists & inhibitors
title Use of electroporation to study the cytotoxic effects of fluorodeoxyuridylate in intact cells
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