Mutation at the catalytic site of topoisomerase I in CEM/C2, a human leukemia cell line resistant to camptothecin

Cancer Res. 1995 Mar 15;55(6):1339-46.

Abstract

We developed previously a resistant cell line, CEM/C2, from the human leukemia cell line CCRF-CEM by stepwise selection in camptothecin. This cell line is 974-fold more resistant to camptothecin than parental cells. Resistance is only partially explained by 2-fold reductions in topoisomerase I protein and mRNA levels. We further investigated biochemical and molecular features of topoisomerase I in the resistant cell line. Sequence analyses of the top1 cDNA from CEM/C2 identified mutations corresponding to two amino acid substitutions, Met370Thr and Asn722Ser. Asn722Ser is next to the catalytic Tyr723 in a region highly conserved among type I eukaryotic DNA topoisomerases. Recombinant top1 with the corresponding substitution was found to be catalytically active and resistant to camptothecin. These results indicate that camptothecin resistance of CEM/C2 is due to the mutation Asn722Ser and strongly suggest that the asparagine immediately flanking the catalytic tyrosine is important for the camptothecin action.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Camptothecin / pharmacology*
  • Cricetinae
  • Cricetulus
  • DNA Topoisomerases, Type I / genetics*
  • DNA Topoisomerases, Type I / metabolism
  • Drug Resistance
  • Humans
  • Leukemia / drug therapy*
  • Leukemia / enzymology
  • Leukemia / pathology
  • Molecular Sequence Data
  • Point Mutation
  • Recombinant Proteins / pharmacology
  • Tumor Cells, Cultured

Substances

  • Recombinant Proteins
  • DNA Topoisomerases, Type I
  • Camptothecin

Associated data

  • GENBANK/U07804
  • GENBANK/U07806