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克服紫杉烷类和蒽环类药物耐药性。

Overcoming taxane and anthracycline resistance.

机构信息

Department of Hematology and Oncology, Emory University Winship Cancer Institute, Atlanta, Georgia 30322, USA.

出版信息

Breast J. 2010 May-Jun;16(3):309-12. doi: 10.1111/j.1524-4741.2010.00911.x. Epub 2010 Apr 12.

Abstract

With more and more breast cancer (BC) patients receiving taxanes and anthracyclines in the adjuvant setting, the number of patients resistant to these drugs is rising. Herein, we review cellular mechanisms (e.g., overexpression of drug efflux pumps) that are associated with clinical anthracycline and/or taxane-resistant BC. We also discuss therapeutic approaches that have received Food and Drug Administration approval in this setting or are in clinical development, including targeted agents that do not employ a cytotoxic mechanism, as well as novel chemotherapeutics such as the epothilones, a class of microtubule stabilizers less susceptible to common cellular resistance mechanisms.

摘要

随着越来越多的乳腺癌 (BC) 患者在辅助治疗中接受紫杉烷类和蒽环类药物治疗,对这些药物产生耐药的患者数量正在上升。在此,我们回顾了与临床蒽环类和/或紫杉烷类耐药 BC 相关的细胞机制(例如,药物外排泵的过度表达)。我们还讨论了在该治疗环境下已获得美国食品和药物管理局批准或正在临床开发中的治疗方法,包括不采用细胞毒性机制的靶向药物以及新型化疗药物,如埃坡霉素,这是一类微管稳定剂,较少受到常见细胞耐药机制的影响。

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