ddC- and 3TC-bis(SATE) monophosphate prodrugs overcome cellular resistance mechanisms to HIV-1 associated with cytidine kinase deficiency

Nucleosides Nucleotides. 1999 Apr-May;18(4-5):921-6. doi: 10.1080/15257779908041600.

Abstract

A 2',3'-dideoxycytidine (ddC)-resistant T-lymphoid cell line (MOLT-4/8rddC250), in which deoxycytidine kinase (dCK) gene-expression was decreased when compared with parental cells, has been selected. Cytotoxic and antiretroviral activity of ddC and 3TC was significantly lower in MOLT-4/8rddC250-than in parental MOLT-4/8 cells. ddC- and 3TC-bis(SATE)phosphotriesters completely overcame cellular resistance mechanisms and showed comparable both cytotoxic and antiretroviral activity in parental and ddC-resistant cells.

MeSH terms

  • Base Sequence
  • Cell Line
  • DNA Primers
  • Deoxycytidine Kinase / deficiency*
  • Deoxycytidine Kinase / genetics
  • Drug Resistance, Microbial
  • HIV-1 / drug effects*
  • Humans
  • Lamivudine / pharmacology*
  • Prodrugs / pharmacology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Zalcitabine / pharmacology*

Substances

  • DNA Primers
  • Prodrugs
  • Lamivudine
  • Zalcitabine
  • Deoxycytidine Kinase