miRNA nanotherapeutics for cancer

被引:270
作者
Ganju, Aditya [1 ,2 ]
Khan, Sheema [1 ,2 ]
Hafeez, Bilal B. [1 ,2 ]
Behrman, Stephen W. [3 ]
Yallapu, Murali M. [1 ,2 ]
Chauhan, Subhash C. [1 ,2 ]
Jaggi, Meena [1 ,2 ]
机构
[1] Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA
[2] Univ Tennessee, Hlth Sci Ctr, Ctr Canc Res, Coll Pharm, Memphis, TN 38163 USA
[3] Univ Tennessee, Hlth Sci Ctr, Dept Surg, Memphis, TN 38163 USA
关键词
NEGATIVE BREAST-CANCER; PANCREATIC DUCTAL ADENOCARCINOMA; LINKED PEI NANOCARRIER; TARGETED DELIVERY; PROSTATE-CANCER; LUNG-CANCER; CO-DELIVERY; LIPOPOLYPLEX NANOPARTICLES; HEPATOCELLULAR-CARCINOMA; CHEMOTHERAPEUTIC-AGENTS;
D O I
10.1016/j.drudis.2016.10.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MicroRNAs (miRNAs) are noncoding RNA molecules that regulate gene expression through diverse mechanisms. Increasing evidence suggests that miRNA-based therapies, either restoring or repressing miRNA expression and activity, hold great promise. However, the efficient delivery of miRNAs to target tissues is a major challenge in the transition of miRNA therapy to the clinic. Cationic polymers or viral vectors are efficient delivery agents but their systemic toxicity and immunogenicity limit their clinical usage. Efficient targeting and sustained release of miRNAs/anti-miRNAs using nanoparticles (NPs) conjugated with antibodies and/or peptides could reduce the required therapeutic dosage while minimizing systemic and cellular toxicity. Given their importance in clinical oncology, here we focus on the development of miRNA nanoformulations to achieve enhanced cellular uptake, bioavailability, and accumulation at the tumor site.
引用
收藏
页码:424 / 432
页数:9
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