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
相关论文
共 50 条
  • [11] New generation drugs for treatment of multiple myeloma
    Alanazi, Fehaid
    Kwa, Faith A. A.
    Burchall, Genia
    Jackson, Denise E.
    DRUG DISCOVERY TODAY, 2020, 25 (02) : 367 - 379
  • [12] Novel drugs for the treatment of multiple myeloma: Mechanisms and targets
    Lentzsch, S.
    ONKOLOGIE, 2010, 33 : 19 - 19
  • [13] Therapeutic use of immunomodulatory drugs in the treatment of multiple myeloma
    Raje, Noopur
    Hideshima, Teru
    Anderson, Kenneth C.
    EXPERT REVIEW OF ANTICANCER THERAPY, 2006, 6 (09) : 1239 - 1247
  • [14] Mechanism of immunomodulatory drugs' action in the treatment of multiple myeloma
    Chang, Xiubao
    Zhu, Yuanxiao
    Shi, Changxin
    Stewart, A. Keith
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2014, 46 (03) : 240 - 253
  • [15] Clinical pharmacokinetics of oral drugs in the treatment of multiple myeloma
    Morival, Camille
    Oumari, Sitty
    Lenglet, Arthur
    Le Corre, Pascal
    HEMATOLOGICAL ONCOLOGY, 2018, 36 (03) : 505 - 518
  • [16] Advancements in microenvironment-based therapies: transforming the landscape of multiple myeloma treatment
    Lu, Ke
    Wang, Wen
    Liu, Yuntong
    Xie, Chao
    Liu, Jiye
    Xing, Lijie
    FRONTIERS IN ONCOLOGY, 2024, 14
  • [17] Current status of new drugs for the treatment of patients with multiple myeloma
    Kenealy, M.
    Prince, H. M.
    INTERNAL MEDICINE JOURNAL, 2006, 36 (12) : 781 - 789
  • [18] Refractory multiple myeloma: Count refractory drugs, not lines of treatment!
    Scheid, Christof
    BRITISH JOURNAL OF HAEMATOLOGY, 2023, 202 (01) : 16 - 17
  • [19] Carfilzomib with immunomodulatory drugs for the treatment of newly diagnosed multiple myeloma
    Ola Landgren
    Pieter Sonneveld
    Andrzej Jakubowiak
    Mohamad Mohty
    Karim S. Iskander
    Khalid Mezzi
    David S. Siegel
    Leukemia, 2019, 33 : 2127 - 2143
  • [20] Treatment of multiple myeloma - New drugs raise hope for the future
    Singhal, S
    BRITISH MEDICAL JOURNAL, 2003, 327 (7415): : 575 - 576