Gold-nanobeacons for simultaneous gene specific silencing and intracellular tracking of the silencing events

被引:85
作者
Conde, Joao [1 ,2 ]
Rosa, Joao [1 ,3 ]
de la Fuente, Jesus M. [2 ]
Baptist, Pedro V. [1 ]
机构
[1] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Ciencias Vida, CIGMH, P-2829516 Caparica, Portugal
[2] Univ Zaragoza, Inst Nanociencia Aragon, Zaragoza 50018, Spain
[3] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, REQUIMTE, P-2829516 Caparica, Portugal
关键词
RNA interference; MicroRNAs; Gold-nanobeacons; AntimiRs; Gene silencing; Cancer nanotheranostics; RNA INTERFERENCE; SIRNA; NANOPARTICLES; DELIVERY;
D O I
10.1016/j.biomaterials.2012.12.015
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The potential of a single molecular nanoconjugate to intersect all RNA pathways: from gene specific downregulation to silencing the silencers, i.e. siRNA and miRNA pathways, is demonstrated. Gold-nanobeacons are capable of efficiently silencing single gene expression, exogenous siRNA and endogenous miRNAs while yielding a quantifiable fluorescence signal directly proportional to the level of silencing. The silencing potential is comparable to that of traditional siRNA but the same nanoconjugates structure is also capable of reversing the effect of an exogenous siRNA. We further demonstrate the Gold-nanobeacons' efficiency at targeting and silencing miR-21, an endogenous miRNA involved in cancer development, which could become a valid nanotheranostics approach. Again, expression of miR-21 was inhibited with concomitant increase of the Au-nanobeacons' fluorescence that can be used to assess the silencing effect. This way, a single nanostructure can be used to intersect all RNA regulatory pathways while allowing for direct assessment of effective silencing and cell localization via a quantifiable fluorescence signal, making cancer nanotheranostics possible. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2516 / 2523
页数:8
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