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拓扑异构酶 2α:蒽环类药物疗效的真正预测因子?

Topoisomerase 2 alpha: a real predictor of anthracycline efficacy?

机构信息

Medical Oncology Department, Hospital Clínico San Carlos, Madrid, Spain.

出版信息

Clin Transl Oncol. 2012 Mar;14(3):163-8. doi: 10.1007/s12094-012-0779-1.

Abstract

Anthracyclines are frequently used in the adjuvant setting for breast cancer treatment since it is considered that anthracycline-based chemotherapy treatment benefits breast cancer patients. Nonetheless, these drugs are associated with severe side effects and predictive factors, for sensitivity to anthracyclines, are warranted in clinical practice. Topoisomerase 2 alpha (TOP2A) is considered to be the molecular target of these drugs. The potential predictive value of TOP2A amplification and overexpression has been extensively studied in breast cancer patients treated with anthracyclines. However, results are not conclusive. In this paper, we review some of the published studies addressing the predictive value of TOP2A as well as the cellular functions of this enzyme and its status in breast cancer tissue.

摘要

蒽环类药物常用于乳腺癌的辅助治疗,因为认为蒽环类药物化疗对乳腺癌患者有益。然而,这些药物与严重的副作用有关,因此在临床实践中需要有预测敏感性的因素。拓扑异构酶 2α(TOP2A)被认为是这些药物的分子靶标。在接受蒽环类药物治疗的乳腺癌患者中,TOP2A 扩增和过表达的潜在预测价值已得到广泛研究。然而,结果并不确定。本文回顾了一些已发表的研究,这些研究涉及 TOP2A 的预测价值以及该酶的细胞功能及其在乳腺癌组织中的状态。

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