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人原发性乳腺癌及乳腺癌细胞系中拓扑异构酶IIα与erbB2共扩增:与m-AMSA及米托蒽醌敏感性的关系

Topoisomerase II alpha co-amplification with erbB2 in human primary breast cancer and breast cancer cell lines: relationship to m-AMSA and mitoxantrone sensitivity.

作者信息

Smith K, Houlbrook S, Greenall M, Carmichael J, Harris A L

机构信息

Molecular Oncology Laboratories, Imperial Cancer Research Fund, University of Oxford, UK.

出版信息

Oncogene. 1993 Apr;8(4):933-8.

PMID:8096076
Abstract

Topoisomerase II alpha (topo II alpha) is a key enzyme in DNA replication and a target for many anti-cancer drugs. High levels are associated with sensitivity to topoisomerase II inhibitors. Because its chromosome location is similar to erbB2 (17q21-22), which is frequently amplified in breast cancer, co-amplification of these genes was assessed. In 117 primary breast cancers, 25 were amplified for erbB2. Three of these cases showed co-amplification of topo II alpha. Topo II beta was not amplified. Four human breast cancer cell lines were assessed for erbB2 and topo II alpha co-amplification. They were also analysed for sensitivity to the topoisomerase inhibitors m-AMSA and mitoxantrone. The most sensitive cell line was SKBr3, which was the only one with erbB2 amplification. Topo II alpha was co-amplified to a similar extent as in tumours. This suggests that patients whose tumours show topo II alpha amplification should be assessed specifically for therapy with topoisomerase inhibitors.

摘要

拓扑异构酶IIα(topo IIα)是DNA复制中的关键酶,也是许多抗癌药物的作用靶点。高水平的拓扑异构酶IIα与对拓扑异构酶II抑制剂的敏感性相关。由于其染色体定位与erbB2(17q21 - 22)相似,而erbB2在乳腺癌中经常扩增,因此对这些基因的共扩增情况进行了评估。在117例原发性乳腺癌中,25例erbB2基因扩增。其中3例显示拓扑异构酶IIα基因共扩增。拓扑异构酶IIβ未扩增。对4个人类乳腺癌细胞系进行了erbB2和拓扑异构酶IIα共扩增情况的评估。还分析了它们对拓扑异构酶抑制剂m - AMSA和米托蒽醌的敏感性。最敏感的细胞系是SKBr3,它是唯一erbB2基因扩增的细胞系。拓扑异构酶IIα的共扩增程度与肿瘤中的相似。这表明对于肿瘤显示拓扑异构酶IIα扩增的患者,应专门评估其使用拓扑异构酶抑制剂进行治疗的情况。

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