Nanoparticles for siRNA-Based Gene Silencing in Tumor Therapy

被引:50
|
作者
Babu, Anish [1 ,2 ]
Muralidharan, Ranganayaki [1 ,2 ]
Amreddy, Narsireddy [1 ,2 ]
Mehta, Meghna [2 ,3 ]
Munshi, Anupama [2 ,3 ]
Ramesh, Rajagopal [1 ,2 ,4 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Stephenson Canc Ctr, Oklahoma City, OK 73104 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Radiat Oncol, Oklahoma City, OK 73104 USA
[4] Univ Oklahoma, Hlth Sci Ctr, Grad Program Biomed Sci, Oklahoma City, OK 73104 USA
基金
美国国家卫生研究院;
关键词
Cancer; gene silencing; liposome; nanoparticle; polymer; siRNA; MESOPOROUS SILICA NANOPARTICLES; ACCELERATED BLOOD CLEARANCE; POLYMER-BASED NANOPARTICLE; ENDOTHELIAL GROWTH-FACTOR; OVERCOME DRUG-RESISTANCE; INTERFERING RNA DELIVERY; IN-VIVO; PHOTODYNAMIC THERAPY; LIPID NANOPARTICLES; MEDIATED DELIVERY;
D O I
10.1109/TNB.2016.2621730
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gene silencing through RNA interference (RNAi) has emerged as a potential strategy in manipulating cancer causing genes by complementary base-pairing mechanism. Small interfering RNA (siRNA) is an important RNAi tool that has found significant application in cancer therapy. However due to lack of stability, poor cellular uptake and high probability of loss-of-function due to degradation, siRNA therapeutic strategies seek safe and efficient delivery vehicles for in vivo applications. The current review discusses various nanoparticle systems currently used for siRNA delivery for cancer therapy, with emphasis on liposome based gene delivery systems. The discussion also includes various methods availed to improve nanoparticle based-siRNA delivery with target specificity and superior efficiency. Further this review describes challenges and perspectives on the development of safe and efficient nanoparticle based-siRNA-delivery systems for cancer therapy.
引用
收藏
页码:849 / 863
页数:15
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