Smart functional nucleic acid chimeras: Enabling tissue specific RNA targeting therapy

被引:34
作者
Aaldering, Lukas J. [1 ,2 ]
Tayeb, Hossam [3 ]
Krishnan, Shilpa [4 ]
Fletcher, Susan [5 ,6 ]
Wilton, Stephen D. [5 ,6 ]
Veedu, Rakesh N. [1 ,3 ,5 ,6 ]
机构
[1] Univ Southern Denmark, Nucle Acid Ctr, Dept Phys Chem & Pharm, Odense, Denmark
[2] Univ Munster, Inst Plant Biol & Biotechnol IBBP, D-48149 Munster, Germany
[3] Univ Queensland, Sch Chem & Mol Biosci, Brisbane, Qld, Australia
[4] Odense Univ Hosp, Dept Nucl Med, DK-5000 Odense, Denmark
[5] Murdoch Univ, Ctr Comparat Genom, Perth, WA, Australia
[6] Western Australian Neurosci Res Inst, Murdoch, WA, Australia
关键词
aptamers; siRNA delivery; Aptamer targeted delivery; aptamer chimera; modified nucleotides; miRNA delivery; APTAMER-SIRNA CHIMERAS; IN-VITRO SELECTION; PHI29 MOTOR PRNA; IMMUNODEFICIENCY-VIRUS TYPE-1; SMALL MOLECULE INTERACTION; ELONGATION-FACTOR; HIGH-AFFINITY; CANCER-CELLS; SYSTEMATIC EVOLUTION; MAMMALIAN-CELLS;
D O I
10.1080/15476286.2015.1017234
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
A major obstacle for effective utilization of therapeutic oligonucleotides such as siRNA, antisense, antimiRs etc. is to deliver them specifically to the target tissues. Toward this goal, nucleic acid aptamers are re-emerging as a prominent class of biomolecules capable of delivering target specific therapy and therapeutic monitoring by various molecular imaging modalities. This class of short oligonucleotide ligands with high affinity and specificity are selected from a large nucleic acid pool against a molecular target of choice. Poor cellular uptake of therapeutic oligonucleotides impedes gene-targeting efficacy in vitro and in vivo. In contrast, aptamer-oligonucleotide chimeras have shown the capacity to deliver siRNA, antimiRs, small molecule drugs etc. toward various targets and showed very promising results in various studies on different diseases models. However, to further improve the bio-stability of such chimeric conjugates, it is important to introduce chemically-modified nucleic acid analogs. In this review, we highlight the applications of nucleic acid aptamers for target specific delivery of therapeutic oligonucleotides.
引用
收藏
页码:412 / 425
页数:14
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