Black S M, Beggs J D, Hayes J D, Bartoszek A, Muramatsu M, Sakai M, Wolf C R
Imperial Cancer Research Fund, University of Edinburgh Department of Biochemistry.
Biochem J. 1990 Jun 1;268(2):309-15. doi: 10.1042/bj2680309.
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.
生物对环境中化学物质的适应与抗性是进化过程的关键部分。因此,多种保护细胞免受化学损伤的防御系统得以进化。这类化学抗性机制似乎在决定人类肿瘤对化疗药物治疗的敏感性方面起着核心作用。谷胱甘肽S-转移酶(GST)是重要的解毒酶,其过度表达与耐药性相关。为了评估这种可能性,我们在酿酒酵母中表达了编码GST B1B1和GST pi的人类α类和π类GST cDNA。GST B1B1或GST pi的表达导致双功能烷化剂苯丁酸氮芥和蒽环类药物阿霉素的细胞毒性作用显著降低。这些数据提供了直接证据,表明细胞中GST的过度表达可赋予对抗癌药物的抗性。