Hosking L K, Whelan R D, Shellard S A, Bedford P, Hill B T
Laboratory of Cellular Chemotherapy, Imperial Cancer Research Fund, Lincoln's Inn Fields, London, U.K.
Biochem Pharmacol. 1990 Oct 15;40(8):1833-42. doi: 10.1016/0006-2952(90)90364-q.
Glutathione and its associated enzyme activities have been quantitated in a series of human tumour continuous cell lines expressing a range of in vitro sensitivities to certain antitumour agents. Fourteen different parental lines and 15 various drug- and X-ray-selected resistant sublines have been studied. Quantitative relationships between total glutathione levels and related enzyme activities and sensitivities to six clinically-useful antitumour drugs or X-rays, as judged by colony forming assays, have been determined by linear regression analysis. A positive correlation has been identified between glutathione levels and sensitivities to cisplatin. Adriamycin, or to X-rays. In addition, positive correlations were noted between cisplatin sensitivities and glutathione peroxidase and reductase activities and for Adriamycin responses with respect to glutathione peroxidase activity, using cumene hydroperoxide as substrate. However, no positive correlations were noted for glutathione levels or these enzyme activities with differential methotrexate, etoposide, vincristine or 5-fluorouracil cytotoxicities. Furthermore, no direct relationship was apparent between total glutathione S-transferase activities and any of these drug or X-ray sensitivities in this series of cell lines. These data appear to provide further evidence linking altered glutathione metabolism with differential cytotoxicities of certain clinically-useful antitumour agents.
在一系列对某些抗肿瘤药物具有不同体外敏感性的人肿瘤连续细胞系中,对谷胱甘肽及其相关酶活性进行了定量分析。研究了14种不同的亲本细胞系和15种经药物和X射线筛选的耐药亚系。通过集落形成试验判断,采用线性回归分析确定了总谷胱甘肽水平、相关酶活性与对六种临床常用抗肿瘤药物或X射线敏感性之间的定量关系。已确定谷胱甘肽水平与对顺铂、阿霉素或X射线的敏感性之间呈正相关。此外,以氢过氧化异丙苯为底物时,顺铂敏感性与谷胱甘肽过氧化物酶和还原酶活性之间以及阿霉素反应与谷胱甘肽过氧化物酶活性之间均呈正相关。然而,谷胱甘肽水平或这些酶活性与甲氨蝶呤、依托泊苷、长春新碱或5-氟尿嘧啶的差异细胞毒性之间未发现正相关。此外,在这一系列细胞系中,总谷胱甘肽S-转移酶活性与任何这些药物或X射线敏感性之间均未发现直接关系。这些数据似乎为将改变的谷胱甘肽代谢与某些临床常用抗肿瘤药物的差异细胞毒性联系起来提供了进一步的证据。