RNA aptamer-mediated gene therapy of prostate cancer: lessons from the past and future directions

被引:1
|
作者
Arese, Marco [1 ,2 ]
Mahmoudian, Mohammad [1 ,2 ]
Bussolino, Federico [1 ,2 ]
机构
[1] Univ Torino, Dept Oncol, Candiolo, Italy
[2] IRCCS, FPO, Candiolo Canc Inst, I-10060 Candiolo, Italy
关键词
PSMA; RNA aptamers; gene therapy; prostate cancer; Biostabilization; MEMBRANE ANTIGEN-EXPRESSION; IN-VITRO; VASCULAR-PERMEABILITY; VEGF APTAMER; DNA-PK; PSMA; DELIVERY; CELLS; INHIBITION; NANOPARTICLES;
D O I
10.1080/17425247.2023.2292691
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionProstate cancer (PCa) is one of the most prevalent cancers in the world, and the fifth cause of death from cancer in men. Among the non-surgical treatments for PCa, gene therapy strategies are in the early stages of development and recent clinical trials have provided new insights suggesting promising future.Areas coveredRecently, the creation of targeted gene delivery systems, based on specific PCa cell surface markers, has been viewed as a viable therapeutic approach. Prostate-specific membrane antigen (PSMA) is vastly expressed in nearly all prostate malignancies, and the intensity of expression increases with tumor aggressiveness, androgen independence, and metastasis. RNA aptamers are short and single-stranded oligonucleotides, which selectively bind to a specific ligand on the surface of the cells, which makes them fascinating small molecules for target delivery of therapeutics. PSMA-selective RNA aptamers represent great potential for developing targeted-gene delivery tools for PCa.Expert opinionThis review provides a thorough horizon for the researchers interested in developing targeted gene delivery systems for PCa via PSMA RNA aptamers. In addition, we provided general information about different prospects of RNA aptamers including discovery approaches, stability, safety, and pharmacokinetics.
引用
收藏
页码:1609 / 1621
页数:13
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