Expression of human glutathione S-transferases in Saccharomyces cerevisiae confers resistance to the anticancer drugs adriamycin and chlorambucil

Biochem J. 1990 Jun 1;268(2):309-15. doi: 10.1042/bj2680309.

Abstract

Adaptation and resistance to chemicals in the environment is a critical part of the evolutionary process. As a result, a wide variety of defence systems that protect cells against chemical insult have evolved. Such chemical resistance mechanisms appear to play a central role in determining the sensitivity of human tumours to treatment with chemotherapeutic drugs. The glutathione S-transferases (GST) are important detoxification enzymes whose over-expression has been associated with drug-resistance. In order to evaluate this possibility we have expressed the human Alpha-class and Pi-class GST cDNAs that encode GST B1B1 and GST pi in the yeast Saccharomyces cerevisiae. The expression of GST B1B1 or GST pi resulted in a marked reduction in the cytotoxic effects of chlorambucil, a bifunctional alkylating agent, and an anthracycline, adriamycin. These data provide direct evidence that the over-expression of GST in cells can confer resistance to anticancer drugs.

MeSH terms

  • Alkylating Agents / pharmacology*
  • Chlorambucil / pharmacology*
  • DNA, Fungal / biosynthesis
  • DNA, Recombinant / biosynthesis
  • Doxorubicin / pharmacology*
  • Drug Resistance, Microbial*
  • Escherichia coli / genetics
  • Gene Expression*
  • Glutathione Transferase / biosynthesis
  • Glutathione Transferase / genetics*
  • Microbial Sensitivity Tests
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / enzymology
  • Saccharomyces cerevisiae / genetics*

Substances

  • Alkylating Agents
  • DNA, Fungal
  • DNA, Recombinant
  • Chlorambucil
  • Doxorubicin
  • Glutathione Transferase