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乳腺癌中erbB2、拓扑异构酶IIα和视黄酸受体α基因的共同扩增以及20号染色体上拓扑异构酶I的等位基因缺失。

Co-amplification of erbB2, topoisomerase II alpha and retinoic acid receptor alpha genes in breast cancer and allelic loss at topoisomerase I on chromosome 20.

作者信息

Keith W N, Douglas F, Wishart G C, McCallum H M, George W D, Kaye S B, Brown R

机构信息

CRC Department of Medical Oncology, Beatson Laboratories, Bearsden, Glasgow, U.K.

出版信息

Eur J Cancer. 1993;29A(10):1469-75. doi: 10.1016/0959-8049(93)90022-8.

Abstract

The DNA topoisomerase enzymes are targets for the cytotoxic effects of a number of anticancer agents termed topoisomerase inhibitors. We have analysed breast cancer biopsy specimens for genetic alterations at and around topoisomerase loci in order to obtain molecular insight into factors which may determine how tumours respond to chemotherapy. We show that of 50 tumours examined, the topoisomerase II alpha locus is co-amplified in 3 cases out of 6 with erbB2 amplification and that amplification can be accompanied by high expression of topoisomerase II alpha. In our attempts to distinguish amplification from aneuploidy and define the limits of amplification, we also observed co-amplification of the retinoic acid-alpha receptor with erbB2 and topoisomerase II alpha in the same three samples. At the topoisomerase I locus on chromosome 20, we observed allelic loss in two out of 17 samples. Genetics abberations at topoisomerase loci, therefore, appear to be relatively common in breast cancer.

摘要

DNA拓扑异构酶是多种被称为拓扑异构酶抑制剂的抗癌药物产生细胞毒性作用的靶点。我们分析了乳腺癌活检标本中拓扑异构酶基因座及其周围的基因改变,以便从分子层面深入了解可能决定肿瘤对化疗反应的因素。我们发现,在检测的50个肿瘤中,拓扑异构酶IIα基因座在6例erbB2扩增的肿瘤中有3例发生了共扩增,并且扩增可能伴随着拓扑异构酶IIα的高表达。在我们试图区分扩增与非整倍体并确定扩增范围的过程中,我们还在相同的三个样本中观察到视黄酸-α受体与erbB2和拓扑异构酶IIα发生了共扩增。在20号染色体上的拓扑异构酶I基因座处,我们在17个样本中的2个中观察到了等位基因缺失。因此,拓扑异构酶基因座的遗传畸变在乳腺癌中似乎相对常见。

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