Targeted polymeric nanoparticles for cancer gene therapy

被引:29
|
作者
Kim, Jayoung [1 ,2 ]
Wilson, David R. [1 ,2 ]
Zamboni, Camila G. [1 ,2 ,3 ,4 ]
Green, Jordan J. [1 ,2 ,5 ,6 ,7 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Translat Tissue Engn Ctr, Baltimore, MD USA
[3] Johns Hopkins Med Inst, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD 21205 USA
[4] Univ Sao Paulo, Fac Med, Hosp Clin, Inst Canc Estado Sao Paulo, Sao Paulo, Brazil
[5] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD 21218 USA
[6] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Sch Med, Dept Ophthalmol, Baltimore, MD 21205 USA
基金
美国国家科学基金会;
关键词
Cancer therapy; cell-specificity; gene delivery; nanoparticles; polymeric biomaterial; promoter; targeting ligands; tissue-specificity; MESENCHYMAL STEM-CELLS; IN-VIVO; PLASMID DNA; RNA INTERFERENCE; TRANSGENE EXPRESSION; CELLULAR UPTAKE; IONIZING-RADIATION; PEI/DNA COMPLEXES; MEMBRANE ANTIGEN; MOLECULAR-WEIGHT;
D O I
10.3109/1061186X.2015.1048519
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this article, advances in designing polymeric nanoparticles for targeted cancer gene therapy are reviewed. Characterization and evaluation of biomaterials, targeting ligands, and transcriptional elements are each discussed. Advances in biomaterials have driven improvements to nanoparticle stability and tissue targeting, conjugation of ligands to the surface of polymeric nanoparticles enable binding to specific cancer cells, and the design of transcriptional elements has enabled selective DNA expression specific to the cancer cells. Together, these features have improved the performance of polymeric nanoparticles as targeted non-viral gene delivery vectors to treat cancer. As polymeric nanoparticles can be designed to be biodegradable, non-toxic, and to have reduced immunogenicity and tumorigenicity compared to viral platforms, they have significant potential for clinical use. Results of polymeric gene therapy in clinical trials and future directions for the engineering of nanoparticle systems for targeted cancer gene therapy are also presented.
引用
收藏
页码:627 / 641
页数:15
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