Transcriptional down-regulation of c-myc expression in an erythroleukemic cell line, K562, and its doxorubicin-resistant variant by two topoisomerase II inhibitors, doxorubicin and amsacrine

Anticancer Drugs. 1998 Mar;9(3):245-54. doi: 10.1097/00001813-199803000-00007.

Abstract

We have evaluated the effect of two topoisomerase II (Topo II) poisons, amsacrine and doxorubicin, on the expression of the c-myc oncogene, both at the mRNA and protein levels, in the leukemia cell line, K562, and its doxorubicin-resistant counterpart, K562 DoxR. We report in this study a concentration-dependent decrease in c-myc mRNA levels upon exposure of both cell lines to amsacrine and doxorubicin, with a more pronounced effect for amsacrine in the resistant line. In either case, c-myc down-regulation closely paralleled the drug-induced growth inhibition. We have also used the technique of PCR stop-assay to detect the occurrence of DNA breaks within the P2 promoter of the c-myc gene. We have shown that Topo II-mediated breaks induced by amsacrine are probably responsible for the down-regulation of c-myc in the resistant line. In addition, amsacrine induced apoptosis only in the resistant line while doxorubicin did not induce apoptosis in any cell line. These results suggest that c-myc is not involved in the resistance of K562 DoxR cells, but can induce the apoptosis pathway in these cells, while no drug-induced apoptosis could be detected in the sensitive line.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amsacrine / pharmacology*
  • Apoptosis / drug effects
  • Cell Division / drug effects
  • Cell Nucleus / metabolism
  • DNA Fragmentation
  • DNA Probes
  • Doxorubicin / pharmacology*
  • Drug Resistance, Multiple*
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Genes, myc
  • Humans
  • Leukemia, Erythroblastic, Acute
  • Polymerase Chain Reaction
  • Proto-Oncogene Proteins c-myc / biosynthesis*
  • RNA, Messenger / biosynthesis
  • Topoisomerase II Inhibitors*
  • Transcription, Genetic / drug effects*
  • Tumor Cells, Cultured

Substances

  • DNA Probes
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • Topoisomerase II Inhibitors
  • Amsacrine
  • Doxorubicin