Hill B T, Shellard S A, Hosking L K, Dempke W C, Fichtinger-Schepman A M, Tone T, Scanlon K J, Whelan R D
Laboratory of Cellular Chemotherapy, Imperial Cancer Research Fund, London, United Kingdom.
Cancer Res. 1992 Jun 1;52(11):3110-8.
In vitro exposure of the TR170 ovarian carcinoma cell line to six intermittent 24-h treatments with a 90% inhibitory concentration of cisplatin (CDDP) (0.15 micrograms/ml; 0.5 microM) resulted in a 2-fold stably resistant subline designated TR170/CP+ (B.T. Hill et al., Int. J. Cancer, 39: 219-225, 1987). Resistance to CDDP in these CP+ cells has now been associated with reduced uptake of 195mCDDP (2-fold; P less than 0.01) and decreased removal of specific Pt-DNA adducts, quantitated immunochemically, indicative of an apparent increased tolerance of CDDP-induced DNA damage. Specifically these resistant cells appeared deficient in removal of the major cis-Pt-(NH3)2d(pGpG) adduct and the difunctional cis-Pt(NH3)2d(GMP)2 lesion, showed less efficiency in removing cis-Pt(NH3)2d(pApG) adducts, but proved as proficient as the parental cell line in removing DNA-DNA interstrand cross-links. Activities of DNA polymerase-alpha and -beta were comparable in both lines, and no significant alterations in glutathione metabolism were identified. Response to acute X-irradiation was not modified in these TR170/CP+ cells, but they showed marked (10-fold) cross-resistance to 5-fluorouracil and, unusually, proved collaterally sensitive (12-fold) to methotrexate. Resistance to 5-fluorouracil was associated with significantly increased thymidylate synthase activity (P less than 0.01), but this was not reflected in altered gene expression, while increased sensitivity to methotrexate was accompanied by increased drug uptake but by unaltered activity and expression of dihydrofolate reductase. These results indicate that exposure to CDDP can result in numerous alterations, both intracellularly and at the cellular membrane, reflected in significant changes in the tumor cells' responses to the cytotoxic effects of a range of antitumor drugs. The clinical relevance of these observations remains to be established.
将TR170卵巢癌细胞系在体外暴露于6次间歇性24小时的90%抑制浓度顺铂(CDDP)(0.15微克/毫升;0.5微摩尔)处理后,产生了一个稳定耐药2倍的亚系,命名为TR170/CP+(B.T.希尔等人,《国际癌症杂志》,39: 219 - 225,1987年)。这些CP+细胞对CDDP的耐药性现在与195mCDDP摄取减少(2倍;P<0.01)以及通过免疫化学定量的特定铂 - DNA加合物清除减少有关,这表明对CDDP诱导的DNA损伤的耐受性明显增加。具体而言,这些耐药细胞在清除主要的顺铂 - (NH3)2d(pGpG)加合物和双功能顺铂(NH3)2d(GMP)2损伤方面似乎存在缺陷,在清除顺铂(NH3)2d(pApG)加合物方面效率较低,但在清除DNA - DNA链间交联方面与亲代细胞系一样熟练。两系中DNA聚合酶α和β的活性相当,未发现谷胱甘肽代谢有显著改变。这些TR170/CP+细胞对急性X射线照射的反应未改变,但它们对5 - 氟尿嘧啶表现出显著的(10倍)交叉耐药性,并且不同寻常的是,对甲氨蝶呤表现出协同敏感性(12倍)。对5 - 氟尿嘧啶的耐药性与胸苷酸合成酶活性显著增加(P<0.01)有关,但这并未反映在基因表达改变上,而对甲氨蝶呤的敏感性增加伴随着药物摄取增加,但二氢叶酸还原酶的活性和表达未改变。这些结果表明,暴露于CDDP可导致细胞内和细胞膜上的众多改变,这反映在肿瘤细胞对一系列抗肿瘤药物细胞毒性作用的反应发生显著变化。这些观察结果的临床相关性仍有待确定。