Literature DB >> 139166

The relationship between DNA strand-scission and DNA synthesis inhibition in HeLa cells treated with neocarzinostatin.

T A Beerman, I H Goldberg.   

Abstract

Neocarzinostatin inhibits DNA synthesis in HeLa S3 cells and induces the rapid limited breakage of cellular DNA. The fragmentation of cellular DNA appears to precede the inhibition of DNA synthesis. Cells treated with drug at 37 degrees C for 10 min and then washed free of drug show similar levels of inhibition of DNA synthesis or cell growth, or of strand-scission of DNA as when cells were not washed. If cells are preincubated with neocarzinostatin at 0 degrees C before washing, the subsequent incubation of 37 degrees C results in no inhibition of DNA synthesis or cell growth, or cutting of DNA. Isolated nuclei or cell lysates derived from neocarzinostatin-treated HeLa S3 cells are inhibited in DNA synthesis but this can be overcome in cell lysates by adding activated DNA. A cytoplasmic fraction from drug-treated cells can stimulate DNA synthesis by nuclei isolated from untreated cells, whereas nuclei from drug-treated cells are not stimulated by the cytoplasmic fraction from untreated cells. By contrast, neocarzinostatin does not inhibit DNA synthesis when incubated with isolated nuclei, but it can be shown that under these conditions the DNA is already degraded and is not further fragmented by the drug. These data suggest that the drug's ability to induce breakage of cellular DNA in HeLa S3 cells is an essential aspect of its inhibition of DNA replication and may be responsible for the cytotoxic and growth-inhibiting actions of neocarzinostatin.

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Year:  1977        PMID: 139166     DOI: 10.1016/0005-2787(77)90019-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  7 in total

1.  Nucleotide specificity in DNA scission by neocarzinostatin.

Authors:  T Hatayama; I H Goldberg; M Takeshita; A P Grollman
Journal:  Proc Natl Acad Sci U S A       Date:  1978-08       Impact factor: 11.205

2.  Sequence specific cleavage of DNA by the antitumor antibiotics neocarzinostatin and bleomycin.

Authors:  A D D'Andrea; W A Haseltine
Journal:  Proc Natl Acad Sci U S A       Date:  1978-08       Impact factor: 11.205

3.  Activation and inactivation of neocarzinostatin-induced cleavage of DNA.

Authors:  L S Kappen; I H Goldberg
Journal:  Nucleic Acids Res       Date:  1978-08       Impact factor: 16.971

4.  An uptake of fluorescein isothiocyanate labeled neocarzinostatin into the cancer and normal cells.

Authors:  S Sakamoto; H Maeda; J Ogata
Journal:  Experientia       Date:  1979-09-15

5.  Distribution and specificity of mutations induced by neocarzinostatin in the lacI gene of Escherichia coli.

Authors:  P L Foster; E Eisenstadt
Journal:  J Bacteriol       Date:  1983-01       Impact factor: 3.490

6.  DNA double strand breaks but not interstrand crosslinks prevent progress through meiosis in fully grown mouse oocytes.

Authors:  Wai Shan Yuen; Julie A Merriman; Moira K O'Bryan; Keith T Jones
Journal:  PLoS One       Date:  2012-08-22       Impact factor: 3.240

7.  Poly(ADP-ribose) polymerase (PARP-1) is not involved in DNA double-strand break recovery.

Authors:  Georges Noël; Nicole Giocanti; Marie Fernet; Frédérique Mégnin-Chanet; Vincent Favaudon
Journal:  BMC Cell Biol       Date:  2003-07-16       Impact factor: 4.241

  7 in total

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