Lipid nanoparticles-based RNA therapies for breast cancer treatment

被引:0
|
作者
Serpico, Luigia [1 ]
Zhu, Yuewen [1 ]
Maia, Renata Faria [1 ]
Sumedha, Sumedha [1 ]
Shahbazi, Mohammad-Ali [1 ]
Santos, Helder A. [1 ,2 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen UMCG, Personalized Med Res Inst PRECIS, Dept Biomat & Biomed Technol, Groningen, Netherlands
[2] Univ Helsinki, Fac Pharm, Drug Res Program, Div Pharmaceut Chem & Technol, Helsinki, Finland
关键词
Breast cancer; RNA technologies; Lipid nanoparticles; Clinical applications; Gene therapy; MESSENGER-RNA; SIRNA DELIVERY; IN-VITRO; INTRACELLULAR DELIVERY; ENDOSOMAL ESCAPE; CATIONIC LIPIDS; DRUG-DELIVERY; GENE-TRANSFER; THERAPEUTICS; PROTEINS;
D O I
10.1007/s13346-024-01638-2
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Breast cancer (BC) prevails as a major burden on global healthcare, being the most prevalent form of cancer among women. BC is a complex and heterogeneous disease, and current therapies, such as chemotherapy and radiotherapy, frequently fall short in providing effective solutions. These treatments fail to mitigate the risk of cancer recurrence and cause severe side effects that, in turn, compromise therapeutic responses in patients. Over the last decade, several strategies have been proposed to overcome these limitations. Among them, RNA-based technologies have demonstrated their potential across various clinical applications, notably in cancer therapy. However, RNA therapies are still limited by a series of critical issues like off-target effect and poor stability in circulation. Thus, novel approaches have been investigated to improve the targeting and bioavailability of RNA-based formulations to achieve an appropriate therapeutic outcome. Lipid nanoparticles (LNPs) have been largely proven to be an advantageous carrier for nucleic acids and RNA. This perspective explores the most recent advances on RNA-based technology with an emphasis on LNPs' utilization as effective nanocarriers in BC therapy and most recent progresses in their clinical applications.
引用
收藏
页码:2823 / 2844
页数:22
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