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一种新型蛋白酶体抑制剂NPI-0052作为抗癌疗法。

A novel proteasome inhibitor NPI-0052 as an anticancer therapy.

作者信息

Chauhan D, Hideshima T, Anderson K C

机构信息

Department of Medical Oncology, Harvard Medical School, Dana Farber Cancer Institute, The Jerome Lipper Multiple Myeloma Center, Boston, MA 02115, USA.

出版信息

Br J Cancer. 2006 Oct 23;95(8):961-5. doi: 10.1038/sj.bjc.6603406.

Abstract

Proteasome inhibitor Bortezomib/Velcade has emerged as an effective anticancer therapy for the treatment of relapsed and/or refractory multiple myeloma (MM), but prolonged treatment can be associated with toxicity and development of drug resistance. In this review, we discuss the recent discovery of a novel proteasome inhibitor, NPI-0052, that is distinct from Bortezomib in its chemical structure, mechanisms of action, and effects on proteasomal activities; most importantly, it overcomes resistance to conventional and Bortezomib therapies. In vivo studies using human MM xenografts shows that NPI-0052 is well tolerated, prolongs survival, and reduces tumour recurrence. These preclinical studies provided the basis for Phase-I clinical trial of NPI-0052 in relapsed/refractory MM patients.

摘要

蛋白酶体抑制剂硼替佐米/万珂已成为治疗复发和/或难治性多发性骨髓瘤(MM)的一种有效抗癌疗法,但长期治疗可能会伴有毒性和耐药性的产生。在本综述中,我们讨论了一种新型蛋白酶体抑制剂NPI-0052的最新发现,它在化学结构、作用机制以及对蛋白酶体活性的影响方面与硼替佐米不同;最重要的是,它克服了对传统疗法和硼替佐米疗法的耐药性。使用人MM异种移植进行的体内研究表明,NPI-0052耐受性良好,可延长生存期并减少肿瘤复发。这些临床前研究为NPI-0052在复发/难治性MM患者中进行I期临床试验提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a978/2360698/e2310bf3a64e/95-6603406f1.jpg

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