Immunoproteasome-selective inhibitors: An overview of recent developments as potential drugs for hematologic malignancies and autoimmune diseases

被引:31
作者
Xi, Jianjun [1 ]
Zhuang, Rangxiao [1 ]
Kong, Limin [2 ]
He, Ruoyu [1 ]
Zhu, Huajian [3 ]
Zhang, Jiankang [3 ]
机构
[1] Hangzhou Xixi Hosp, Dept Pharmaceut Preparat, Hangzhou 310023, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, Dept Pharm, Hangzhou 310003, Zhejiang, Peoples R China
[3] Zhejiang Univ City Coll, Sch Med, Hangzhou 310015, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Immunoproteasome inhibitors; Selective; Hematologic malignancies; Autoimmune diseases; KZR-616; UBIQUITIN-PROTEASOME SYSTEM; STRUCTURE-BASED DESIGN; CRYSTAL-STRUCTURE; MULTIPLE-MYELOMA; 20S PROTEASOME; NONCOVALENT PROTEASOME; PROTEIN HOMEOSTASIS; BORTEZOMIB; SUBUNIT; SPECIFICITY;
D O I
10.1016/j.ejmech.2019.111646
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The immunoproteasome, a specialized form of proteasome, is mainly expressed in lymphocytes and monocytes of jawed vertebrates and responsible for the generation of antigenic peptides for cell-mediated immunity. Overexpression of immunoproteasome have been detected in a wide range of diseases including malignancies, autoimmune and inflammatory diseases. Following the successful approval of constitutive proteasome inhibitors bortezomib, carfllzomib and Ixazomib, and with the clarification of immunoproteasome crystal structure and functions, a variety of immunoproteasome inhibitors were discovered or rationally developed. Not only the inhibitory activities, the selectivities for immunoproteasome over constitutive proteasome are essential for the clinical potential of these analogues, which has been validated by the clinical evaluation of immunoproteasome-selective inhibitor KZR-616 for the treatment of systemic lupus erythematosus. In this review, structure, function as well as the current developments of various inhibitors against immunoproteasome are going to be summarized, which help to fully understand the target for drug discovery. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
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页数:17
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