Nonviral Delivery Systems for Cancer Gene Therapy: Strategies and Challenges

被引:48
|
作者
Shim, Gayong [1 ,2 ]
Kim, Dongyoon
Quoc-Viet Le
Park, Gyu Thae
Kwon, Taekhyun
Oh, Yu-Kyoung [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Pharm, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Res Inst Pharmaceut Sci, 1 Gwanak Ro, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
Cancer gene therapy; Nonviral gene therapy; Nonviral delivery; Target cancer gene; Macromolecular; DNA; IN-VIVO; CO-DELIVERY; CPG OLIGONUCLEOTIDE; EFFICIENT DELIVERY; HUMAN-PAPILLOMAVIRUS; PLGA NANOPARTICLES; GOLD NANOPARTICLES; TARGETED DELIVERY; RNA INTERFERENCE; GRAPHENE OXIDE;
D O I
10.2174/1566523218666180119121949
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene therapy has been receiving widespread attention due to its unique advantage in regulating the expression of specific target genes. In the field of cancer gene therapy, modulation of gene expression has been shown to decrease oncogenic factors in cancer cells or increase immune responses against cancer. Due to the macromolecular size and highly negative physicochemical features of plasmid DNA, efficient delivery systems are an essential ingredient for successful gene therapy. To date, a variety of nanostructures and materials have been studied as nonviral gene delivery systems. In this review, we will cover nonviral delivery strategies for cancer gene therapy, with a focus on target cancer genes and delivery materials. Moreover, we will address current challenges and perspectives for nonviral delivery-based cancer gene therapeutics.
引用
收藏
页码:3 / 20
页数:18
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