Houlbrook S, Addison C M, Davies S L, Carmichael J, Stratford I J, Harris A L, Hickson I D
Molecular Oncology Laboratories, Imperial Cancer Research Fund, John Radcliffe Hospital, Oxford, UK.
Br J Cancer. 1995 Dec;72(6):1454-61. doi: 10.1038/bjc.1995.529.
Topoisomerase II is a key target for many anti-cancer drugs used to treat breast cancer. In human cells there are two closely related, but differentially expressed, topoisomerase II isoforms, designated topoisomerase II alpha and beta. Here, we report the production of a new polyclonal antibody raised against a fragment of the C-terminal domain of the 180 kDa form of topoisomerase II (the beta isoform), which does not cross-react with the 170 kDa form (the alpha isoform). Using this antibody, together with a polyclonal antibody specific for the 170 kDa isoform of topoisomerase II, we have examined the relationship between the sensitivity of a panel of human breast cancer cell lines to different classes of topoisomerase II inhibitors and cellular levels of the topoisomerase II alpha and beta proteins. We found that sensitivity to amsacrine showed a correlation with the level of expression of topoisomerase II alpha protein, and that sensitivity to etoposide showed a similar correlation with the level of expression of topoisomerase II beta protein. There was also a relationship between sensitivity of these cell lines to mitoxantrone and the cellular level of both isoforms of topoisomerase II. No relationship was found between the level of mRNA for topoisomerase II alpha or beta, and either sensitivity of breast cancer cell lines to topoisomerase II inhibitors or the level of topoisomerase II protein expression.
拓扑异构酶II是许多用于治疗乳腺癌的抗癌药物的关键靶点。在人类细胞中,有两种密切相关但表达存在差异的拓扑异构酶II亚型,分别称为拓扑异构酶IIα和β。在此,我们报告了一种新的多克隆抗体的产生,该抗体是针对180 kDa形式的拓扑异构酶II(β亚型)的C末端结构域片段产生的,它与170 kDa形式(α亚型)不发生交叉反应。使用该抗体以及针对拓扑异构酶II 170 kDa亚型的特异性多克隆抗体,我们研究了一组人类乳腺癌细胞系对不同类型拓扑异构酶II抑制剂的敏感性与拓扑异构酶IIα和β蛋白细胞水平之间的关系。我们发现,对安吖啶的敏感性与拓扑异构酶IIα蛋白的表达水平相关,对依托泊苷的敏感性与拓扑异构酶IIβ蛋白的表达水平也呈现类似的相关性。这些细胞系对米托蒽醌的敏感性与拓扑异构酶II两种亚型的细胞水平之间也存在关系。未发现拓扑异构酶IIα或β的mRNA水平与乳腺癌细胞系对拓扑异构酶II抑制剂的敏感性或拓扑异构酶II蛋白表达水平之间存在关联。