Literature DB >> 78722

Effect of antabuse (disulfiram) on Rous sarcoma virus and on eukaryotic cells.

W Levinson, P Mikelens, H Oppermann, J Jackson.   

Abstract

Antabuse (disulfiram) is widely used in the treatment of chronic alcoholism. We have examined the effect of this drug on malignant transformation by Rous sarcoma virus, on eukaryotic cell synthesis, and on nucleic acid binding. It was found that: (1) Disulfiram inhibits the activity of the RNA dependent DNA polymerase of Rous sarcoma virus and inactivates the ability of the virus to malignantly transform chick embryo cells. The monomer of disulfiram, diethyldithiocarbamate does not affect the virus. (2) Disulfiram induced the synthesis of four proteins in normal chick embryo and human foreskin cells. The monomer diethyldithiocarbamate, induced these proteins also. Cellular DNA synthesis is more sensitive to disulfiram than are RNA and protein synthesis. (3) Disulfiram binds to neither DNA or RNA in the presence or absence of copper. However, diethyldithiocarbamate in the presence of, but not in the absence of, copper binds to HeLa cell DNA and to Rous sarcoma virus 70 S genome RNA. These results indicate that this compound, which causes no symptoms in people who do not consume alcohol, may have significant effects on a cellular level.

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Year:  1978        PMID: 78722     DOI: 10.1016/0005-2787(78)90062-x

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


  10 in total

1.  Axonal transport of a heat shock protein in the rabbit visual system.

Authors:  B D Clark; I R Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

2.  A cellular protein that associates with the transforming protein of Rous sarcoma virus is also a heat-shock protein.

Authors:  H Oppermann; W Levinson; J M Bishop
Journal:  Proc Natl Acad Sci U S A       Date:  1981-02       Impact factor: 11.205

3.  Heat shock protein in mammalian brain and other organs after a physiologically relevant increase in body temperature induced by D-lysergic acid diethylamide.

Authors:  J W Cosgrove; I R Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1983-01       Impact factor: 11.205

4.  Macromolecular synthesis at the early stage of herpes simplex virus type 2 (HSV-2) latency in a human neuroblastoma cell line IMR-32: repression of late viral polypeptide synthesis and accumulation of cellular heat-shock proteins.

Authors:  Y Yura; K Terashima; H Iga; Y Kondo; T Yanagawa; H Yoshida; Y Hayashi; M Sato
Journal:  Arch Virol       Date:  1987       Impact factor: 2.574

5.  Herpes simplex virus type 1 persistence and latency in cultured rabbit corneal epithelial cells, keratocytes, and endothelial cells.

Authors:  S D Cook; S M Brown
Journal:  Br J Ophthalmol       Date:  1986-09       Impact factor: 4.638

6.  Heat shock proteins are methylated in avian and mammalian cells.

Authors:  C Wang; R H Gomer; E Lazarides
Journal:  Proc Natl Acad Sci U S A       Date:  1981-06       Impact factor: 11.205

7.  Metal binding drugs induce synthesis of four proteins in normal cells.

Authors:  W Levinson; J Idriss; J Jackson
Journal:  Biol Trace Elem Res       Date:  1979-03       Impact factor: 3.738

8.  A major heat-shock protein defined by a monoclonal antibody.

Authors:  N B LaThangue
Journal:  EMBO J       Date:  1984-08       Impact factor: 11.598

9.  Herpes simplex virus infection causes the accumulation of a heat-shock protein.

Authors:  N B LaThangue; K Shriver; C Dawson; W L Chan
Journal:  EMBO J       Date:  1984-02       Impact factor: 11.598

10.  Cell cycle specific radiosensitisation by the disulfiram and copper complex.

Authors:  Mathias Tesson; Giorgio Anselmi; Caitlin Bell; Robert Mairs
Journal:  Oncotarget       Date:  2017-07-25
  10 in total

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