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蛋白酶体抑制剂:血液系统恶性肿瘤的一种治疗策略。

Proteasome inhibitors: a therapeutic strategy for haematological malignancy.

作者信息

Crawford Lisa Judith-Ann, Walker Brian, Irvine Alexandra Elizabeth

机构信息

Haematology, Centre for Cancer Research and Cell Biology, Queen's University Belfast, 97 Lisburn Road, Belfast, BT9 7BL.

出版信息

Front Biosci. 2008 May 1;13:4285-96. doi: 10.2741/3005.

Abstract

The proteasome is a multicatalytic enzyme complex responsible for the regulated degradation of intracellular proteins. In recent years, inhibition of proteasome function has emerged as a novel anti-cancer therapy. Proteasome inhibition is now established as an effective treatment for relapsed and refractory multiple myeloma and offers great promise for the treatment of other haematological malignancies, when used in combination with conventional therapeutic agents. Bortezomib is the first proteasome inhibitor to be used clinically and a second generation of proteasome inhibitors with differential pharmacological properties are currently in early clinical trials. This review summarises the development of proteasome inhibitors as therapeutic agents and describes how novel assays for measuring proteasome activity and inhibition may help to further delineate the mechanisms of action of different proteasome inhibitors. This will allow for the optimized use of proteasome inhibitors in combination therapies and provide the opportunity to design more potent and therapeutically efficacious proteasome inhibitors.

摘要

蛋白酶体是一种多催化酶复合体,负责细胞内蛋白质的有序降解。近年来,抑制蛋白酶体功能已成为一种新型抗癌疗法。蛋白酶体抑制现已被确立为复发难治性多发性骨髓瘤的有效治疗方法,并且在与传统治疗药物联合使用时,为治疗其他血液系统恶性肿瘤带来了巨大希望。硼替佐米是首个用于临床的蛋白酶体抑制剂,目前具有不同药理特性的第二代蛋白酶体抑制剂正处于早期临床试验阶段。本综述总结了蛋白酶体抑制剂作为治疗药物的发展情况,并描述了用于测量蛋白酶体活性和抑制作用的新型检测方法如何有助于进一步阐明不同蛋白酶体抑制剂的作用机制。这将有助于在联合治疗中优化蛋白酶体抑制剂的使用,并为设计更有效和治疗效果更佳的蛋白酶体抑制剂提供机会。

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