1985
DOI: 10.1016/0027-5107(85)90007-7
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Mitomycin C effects on cell cycle progression, including inhibition of very late prophase, as seen in living neuroblasts of Chortophaga viridifasciata, with some observations on mitomycin C purity☆

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Cited by 8 publications
(4 citation statements)
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“…As a result of this, the DNA of each cell gathers thousands of lesions every day. These accumulated lessions or extensive damage can cause various diseases or abnormalities such as cancer [2], tumor development, arrest cell cycle progression [3] .This DNA damaged should be removed so that the cell function and proliferate normally [1,4]. This damage essential to be repaired to allow polymerases (RNA and DNA) to precisely read and duplicate the information in the genome.…”
Section: Introductionmentioning
confidence: 99%
“…As a result of this, the DNA of each cell gathers thousands of lesions every day. These accumulated lessions or extensive damage can cause various diseases or abnormalities such as cancer [2], tumor development, arrest cell cycle progression [3] .This DNA damaged should be removed so that the cell function and proliferate normally [1,4]. This damage essential to be repaired to allow polymerases (RNA and DNA) to precisely read and duplicate the information in the genome.…”
Section: Introductionmentioning
confidence: 99%
“…In vivo, the reversible inhibition of mitosis in very late prophase (Ferguson et al, 1985;Gaulden et al, 1985) corresponding to the reversible inhibition of tubulin assembly in vitro might result either from an interaction of unactivated MMC with the mitotic spindle or from an interaction of MMC with the nuclear envelope leading to a disconnection of centromeres with the nuclear envelope. The reversibility of this in vivo effect might be related to the reductive metabolism of MMC resulting in a timedependent decrease in the concentration of unactivated MMC.…”
Section: Genotoxic Effects In Yeastmentioning
confidence: 99%
“…In neuroblasts of the grasshopper Chortophaga viridifasciata they observed a pronounced retardation of very late prophase which led to loss of chromosome orientation within the nucleus. This effect on mitosis is reversible and is expressed as an extended duration of very late prophase in relation to MMC concentration and time of exposure (Gaulden et al, 1985). This reversible inhibition of mitosis could be related to an interaction of MMC with a non-DNA target as, for example, the spindle.…”
Section: Introductionmentioning
confidence: 99%
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