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拓扑异构酶IIα和β作为乳腺癌的治疗靶点。

Topoisomerases II alpha and beta as therapy targets in breast cancer.

作者信息

Isaacs R J, Davies S L, Wells N J, Harris A L

机构信息

Imperial Cancer Research Fund, University of Oxford, Institute of Molecular Medicine, John Radcliffe Hospital, UK.

出版信息

Anticancer Drugs. 1995 Apr;6(2):195-211. doi: 10.1097/00001813-199504000-00002.

Abstract

Topoisomerase II enzymes play an essential role in human DNA metabolism. They are also recognized as primary targets of a number of anti-cancer drugs used in the treatment of breast cancer, which remains a leading cause of cancer-related death in women. While topoisomerase inhibitors have produced significant response rates in this disease, their use has been limited both by toxicity and by the development of resistance. In this article we review the extensive work which has not only increased our understanding of the biochemistry and molecular biology of type II topoisomerases but also enabled more rational drug design. Such knowledge should translate into increased clinical efficacy in the treatment of breast cancer and other malignancies.

摘要

拓扑异构酶II在人类DNA代谢中起着至关重要的作用。它们也被认为是用于治疗乳腺癌的多种抗癌药物的主要靶点,而乳腺癌仍是女性癌症相关死亡的主要原因。虽然拓扑异构酶抑制剂在这种疾病中产生了显著的缓解率,但它们的使用受到毒性和耐药性发展的限制。在本文中,我们回顾了大量的研究工作,这些工作不仅增进了我们对II型拓扑异构酶生物化学和分子生物学的理解,还推动了更合理的药物设计。这些知识应能转化为提高乳腺癌和其他恶性肿瘤治疗的临床疗效。

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