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Current Status and Perspectives of Protease Inhibitors and Their Combination with Nanosized Drug Delivery Systems for Targeted Cancer Therapy
被引:38
|作者:
Rudzinska, Magdalena
[1
]
Daglioglu, Cenk
[2
]
Savvateeva, Lyudmila, V
[1
]
Kaci, Fatma Necmiye
[3
]
Antoine, Rodolphe
[4
]
Zamyatnin, Andrey A., Jr.
[1
,5
,6
]
机构:
[1] Sechenov First Moscow State Med Univ, Inst Mol Med, Moscow 119991, Russia
[2] Izmir Inst Technol, Integrated Res Ctr, Biotechnol & Bioengn Applicat & Res Ctr, Izmir, Turkey
[3] Erzurum Tech Univ, Fac Sci, Dept Mol Biol & Genet, Erzurum, Turkey
[4] Univ Lyon, Univ Claude Bernard Lyon 1, CNRS, Inst Lumiere Matiere, F-69622 Lyon, France
[5] Lomonosov Moscow State Univ, Belozersky Inst Phys Chem Biol, Moscow 119991, Russia
[6] Sirius Univ Sci & Technol, Dept Biotechnol, Soci 354340, Russia
来源:
DRUG DESIGN DEVELOPMENT AND THERAPY
|
2021年
/
15卷
基金:
俄罗斯科学基金会;
关键词:
proteases;
inhibitors;
nanoscale drug-delivery system;
combination therapy;
cancer treatment;
MATRIX-METALLOPROTEINASE INHIBITORS;
PLASMINOGEN-ACTIVATOR;
CATHEPSIN-B;
ASPARTIC PROTEASE;
CRYSTAL-STRUCTURE;
ARSENIC TRIOXIDE;
TUMOR;
NANOPARTICLES;
PROTEOLYSIS;
FUTURE;
D O I:
10.2147/DDDT.S285852
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
In cancer treatments, many natural and synthetic products have been examined; among them, protease inhibitors are promising candidates for anti-cancer agents. Since dysregulated proteolytic activities can contribute to tumor development and metastasis, antagonization of proteases with tailored inhibitors is an encouraging approach. Although adverse effects of early designs of these inhibitors disappeared after the introduction of next-generation agents, most of the proposed inhibitors did not pass the early stages of clinical trials due to their nonspecific toxicity and lack of pharmacological effects. Therefore, new applications that modulate proteases more specifically and serve their programmed way of administration are highly appreciated. In this context, nanosized drug delivery systems have attracted much attention because preliminary studies have demonstrated that the therapeutic capacity of inhibitors has been improved significantly with encapsulated formulation as compared to their free forms. Here, we address this issue and discuss the current application and future clinical prospects of this potential combination towards targeted protease-based cancer therapy.
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页码:9 / 20
页数:12
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