Dideoxycytidine, an anti-HIV drug, selectively inhibits growth but not phosphatidylcholine metabolism in neuroblastoma and glioma cells

Neurochem Res. 1989 Mar;14(3):279-84. doi: 10.1007/BF00971324.

Abstract

Dideoxycytidine (ddCyd), an inhibitor of AIDS-related HIV, has been examined for effects on cell proliferation and phosphatidylcholine synthesis in tumor lines of nervous system origin. Uptake and metabolism of [3H]ddCyd, observed in all cells, was greatest in one human neuroblastoma line, HTB-10. Growth of the HTB-10 line was markedly inhibited by 40 microM ddCyd, whereas growth of C6 glioma and N1E-115 or HTB-11 neuroblastoma cells was unaltered. Phosphatidylcholine synthesis in the presence or absence of stimulation by phorbol ester was not specifically altered by ddCyd. Thus, ddCyd was incorporated and inhibited growth in a cell-specific manner but had little effect on cytidine-dependent phospholipid synthesis. This suggests that some cells derived from the nervous system may be more susceptible than others with respect to the positive and negative effects of ddCyd as a potential antiviral drug.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Division / drug effects
  • Dideoxynucleosides / pharmacology*
  • Glioma*
  • Humans
  • Neuroblastoma*
  • Phosphatidylcholines / metabolism*
  • Tumor Cells, Cultured / cytology
  • Tumor Cells, Cultured / metabolism*
  • Zalcitabine

Substances

  • Dideoxynucleosides
  • Phosphatidylcholines
  • Zalcitabine