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[多发性骨髓瘤对硼替佐米耐药分子机制的研究进展——综述]

[Research Progress on Molecular Mechanisms of Resistance to Bortezomib in Multiple Myeloma- Review].

作者信息

Shi Ling-Ling, Zhai Yong-Ping

机构信息

Department of Hematology, Nanjing General Hospital, Nanjing 210002, Jiangsu Province, China.

Department of Hematology, Nanjing General Hospital, Nanjing 210002, Jiangsu Province, China . E-mail:ypzhai@medmail. com.cn.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Oct;25(5):1576-1579. doi: 10.7534/j.issn.1009-2137.2017.05.052.

Abstract

Over the last decade, bortezomib(BTZ) has been extensively applied in the treatment of hematological malignancies, particularly in multiple myeloma and mantle cell lymphoma, however, the appearence of secondary resistance to BTZ has brought a huge challenge in MM treatment. In the present review, the mechanisms of resistance to bortezomib in MM are summarized, focusing on the action of ubiquitin-proteasome system(UPS), endoplasmin reticulum stress, antophagy, inducible pro-survival signalling and bone marrow microenvironment as well as exploration of the potential therapeutic strategies in the clinical perspective. With the understanding of the molecular mechanisms for resistance to BTZ, the novel histone deacetylase inhibitors(HDACi) have been approved for the treatment of replased/refractory MM and AKT inhibitor in the clinical trials. These novel combined therapies can enhance BTZ efficiency and improve the outcome of the patients.

摘要

在过去十年中,硼替佐米(BTZ)已被广泛应用于血液系统恶性肿瘤的治疗,尤其是在多发性骨髓瘤和套细胞淋巴瘤的治疗中。然而,对BTZ继发性耐药的出现给多发性骨髓瘤的治疗带来了巨大挑战。在本综述中,总结了多发性骨髓瘤中对硼替佐米耐药的机制,重点关注泛素-蛋白酶体系统(UPS)、内质网应激、自噬、诱导性生存信号和骨髓微环境的作用,以及从临床角度探索潜在的治疗策略。随着对BTZ耐药分子机制的了解,新型组蛋白去乙酰化酶抑制剂(HDACi)已被批准用于治疗复发/难治性多发性骨髓瘤,并且AKT抑制剂已进入临床试验阶段。这些新型联合疗法可以提高BTZ的疗效,改善患者的治疗结果。

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