Advancements in drugs restructured with nanomedicines for multiple myeloma treatment

被引:1
|
作者
Liu, Zhaoyun [1 ,2 ,3 ]
Shen, Hongli [1 ,2 ,3 ]
Liu, Hui [1 ,2 ,3 ]
Ding, Kai [1 ,2 ,3 ]
Song, Jia [1 ,2 ,3 ]
Zhang, Jingtian [4 ,5 ]
Ding, Dan [4 ,5 ]
Fu, Rong [1 ,2 ,3 ]
机构
[1] Tianjin Med Univ, Gen Hosp, Dept Hematol, Tianjin 300052, Peoples R China
[2] Tianjin Key Lab Bone Marrow Failure & Malignant He, Tianjin 300052, Peoples R China
[3] Tianjin Inst Hematol, Tianjin 300052, Peoples R China
[4] Nankai Univ, State Key Lab Med Chem Biol, Key Lab Bioact Mat, Minist Educ, Tianjin 300071, Peoples R China
[5] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
plasma cell disease; nanotechnology; hematology; proteasome inhibitors; OVERCOMES MULTIDRUG-RESISTANCE; AGGREGATION-INDUCED EMISSION; MYRICETIN INDUCES APOPTOSIS; IN-VIVO; TARGETED NANOPARTICLES; THERAPEUTIC-EFFICACY; MONOCLONAL-ANTIBODY; ANTITUMOR-ACTIVITY; ENHANCED EFFICACY; CELLULAR UPTAKE;
D O I
10.1007/s40843-024-3077-0
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Multiple myeloma (MM) is an incurable malignancy of clonal plasma cells, characterized by high relapse rates and rapid development of drug resistance. The emergence of proteasome inhibitors has dramatically improved the therapeutic effect of MM; however, side effects and drug resistance still negatively affect the survival rate of MM. Nano-medicine has become a promising field for therapeutic innovation owing to its biodegradability and biocompatibility. Nanoparticles (NPs), when combined with MM therapeutic drugs, can reduce side effects, increase treatment efficacy, and alleviate drug resistance, providing a new direction for the treatment of MM. Restructuring drugs with NPs presents an ideal strategy for ongoing studies aimed at more effective therapies. Additionally, clinical nanomedicine research has yielded new opportunities for MM treatment. This review, guided by the development of MM therapeutic drugs, summarizes the past 20 years of research progress and breakthroughs in NP-based systems for treating MM and improving drug targeting ability.
引用
收藏
页码:3780 / 3795
页数:16
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