Takeda S, Shimazoe T, Sato K, Sugimoto Y, Tsuruo T, Kono A
Division of Chemotherapy, National Kyushu Cancer Center, Fukuoka, Japan.
Biochem Biophys Res Commun. 1992 Apr 30;184(2):618-25. doi: 10.1016/0006-291x(92)90634-w.
RNA/PCR quantitation method was developed to determine DNA Topoisomerase I(Topo I)-specific mRNA in order to study its gene expression in CPT-11 sensitive, acquired- or native-resistant human pancreatic tumor cell lines. The results were supported by Northern blotting and Western blotting analyses. Acquired-resistant cells have shown decreased levels of Topo I mRNA, compared with their parental cells. On the contrary, in the wild type cells no correlation was shown between sensitivity and gene expression. On the other, specific Topo I activity of the native resistant cell lines was fairly lower than that of sensitive cell lines, suggesting that immunoreactive Topo I protein contains low levels of active form enzyme which could be targets of CPT-11 in these native-resistant ones. Finally, the different mechanisms might be operative between acquired- and native-resistant tumor cells.
开发了RNA/PCR定量方法来测定DNA拓扑异构酶I(Topo I)特异性mRNA,以研究其在CPT - 11敏感、获得性或天然耐药的人胰腺肿瘤细胞系中的基因表达。结果得到了Northern印迹和Western印迹分析的支持。与亲代细胞相比,获得性耐药细胞中Topo I mRNA水平降低。相反,在野生型细胞中,敏感性与基因表达之间没有相关性。另一方面,天然耐药细胞系的特异性Topo I活性明显低于敏感细胞系,这表明免疫反应性Topo I蛋白含有低水平的活性形式酶,这些酶可能是CPT - 11在这些天然耐药细胞中的作用靶点。最后,获得性耐药和天然耐药肿瘤细胞之间可能存在不同的作用机制。