Inhibition of xenograft tumor growth in mice by gold nanoparticle-assisted delivery of short hairpin RNAs against Mcl-1L

被引:6
|
作者
Ryou, Sang-Mi [1 ]
Park, Mira [1 ]
Kim, Jong-Myung [2 ]
Jeon, Che Ok [2 ]
Yun, Cheol-Hui [3 ,4 ]
Han, Seung Hyun [5 ,6 ]
Kim, Si Wouk [7 ]
Lee, Younghoon [8 ]
Kim, Sudeok [9 ]
Han, Min Su [9 ]
Bae, Jeehyeon [1 ]
Lee, Kangseok [2 ]
机构
[1] CHA Univ, Coll Pharm, Dept Pharm, Songnam 463836, South Korea
[2] Chung Ang Univ, Sch Biol Sci, Seoul 156756, South Korea
[3] Seoul Natl Univ, Dept Agr Biotechnol, Seoul 151921, South Korea
[4] Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul 151921, South Korea
[5] Seoul Natl Univ, Sch Dent, Dept Oral Microbiol & Immunol, Dent Res Inst, Seoul 110749, South Korea
[6] Seoul Natl Univ, Sch Dent, Program BK21, Seoul 110749, South Korea
[7] Chosun Univ, Dept Environm Engn, Kwangju 501759, South Korea
[8] Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea
[9] Chung Ang Univ, Dept Chem, Seoul 156756, South Korea
关键词
Gold nanoparticle-assisted gene delivery system (AuNP-GDS); Short hairpin RNAs (shRNAs); Xenograft tumor; Mcl-1; GENE DELIVERY; DRUG-DELIVERY; MAMMALIAN-CELLS; VIRAL VECTORS; DNA; THERAPY; MAINTENANCE; EXPRESSION; CHEMISTRY; BIOLOGY;
D O I
10.1016/j.jbiotec.2011.07.037
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A prerequisite for the therapeutic use of small RNAs is the development of a method that can deliver them into animals. Previous studies have shown the capability of functionalized gold nanoparticles to serve as a general platform for loading and delivering DNA oligonucleotides and short hairpin RNAs (shRNAs) into cultured human cells. Here, we report the ability of the gold nanoparticle-assisted gene delivery system (AuNP-GDS) to deliver shRNA to a xenograft tumor in a mouse model. AuNP-GDS delivery of in vitro synthesized shRNA targeted to the Mcl-1L gene knocked down levels of Mcl-1L mRNA and protein by similar to 36% and similar to 26%, respectively, which were sufficient to induce apoptosis of the xenograft tumor cells and consequently inhibited the development of the tumor. We demonstrated that our lego-like AuNP-GDS, which can easily load and deliver shRNAs targeted to any gene of interest into living systems, can deliver shRNAs into xenograft tumors, leading to antitumor activity in an animal model. (C) 2011 Elsevier B. V. All rights reserved.
引用
收藏
页码:89 / 94
页数:6
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