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      Formation of interstrand DNA cross-links by bis-(2-chloroethyl)sulfide (BCES): a possible cytotoxic mechanism in rat keratinocytes.

      Biochemical and Biophysical Research Communications
      Animals, Aphidicolin, pharmacology, Cell Cycle, drug effects, Cell Differentiation, Cells, Cultured, Cross-Linking Reagents, chemistry, DNA, DNA Damage, Dermatologic Agents, Enzyme Inhibitors, Keratinocytes, cytology, Mustard Gas, Nucleic Acid Synthesis Inhibitors, Rats

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          Abstract

          Interstrand cross-links in the DNA of epidermal basal keratinocytes may be responsible for cell death and consequent vesication in skin exposed to BCES. The formation of cross-links and cytotoxicity were compared when cells in primary monolayer cultures of rat epidermal keratinocytes, synchronized at the G1/S boundary or in the G1 phase of the cell cycle, were exposed to BCES. The dose-responsive formation of cross-links, measured with an ethidium bromide-fluorescence assay, was determined immediately after exposure of cells at either position of the cycle. At 24 hr post-exposure, the level of cross-links in cells exposed at the G1 phase showed had not decreased significantly and was still dose-dependent. However, cells exposed in the G1 phase showed a major decrease in cross-links. Formation of interstrand DNA cross-links appears to be related to the mustard's cytotoxicity.

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