Multifunctional Aptamer-miRNA Conjugates for Targeted Cancer Therapy

被引:143
作者
Esposito, Carla L. [1 ]
Cerchia, Laura [1 ]
Catuogno, Silvia [1 ]
De Vita, Gennaro [1 ]
Dassie, Justin P. [2 ]
Santamaria, Gianluca [3 ]
Swiderski, Piotr [4 ]
Condorelli, Gerolama [1 ,5 ]
Giangrande, Paloma H. [2 ,6 ]
de Franciscis, Vittorio [1 ]
机构
[1] CNR, Ist Endocrinol & Oncol Sperimentale, I-80131 Naples, Italy
[2] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[3] Univ Salerno, Lab Med Mol & Genom, I-84100 Salerno, Italy
[4] Beckman Res Inst City Hope, Synthet & Biopolymer Chem Core, Duarte, CA USA
[5] Univ Naples Federico II, Dipartimento Med Mol & Biotecnol Med, Naples, Italy
[6] Univ Iowa, Mol & Cellular Biol Program, Iowa City, IA USA
关键词
IN-VIVO DELIVERY; SIRNA CHIMERAS; INDUCED APOPTOSIS; LET-7; FAMILY; CELLS; INHIBITION; MICRORNAS; EXPRESSION; GROWTH; INDUCTION;
D O I
10.1038/mt.2014.5
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 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
While microRNAs (miRNAs) clearly regulate multiple pathways integral to disease development and progression, the lack of safe and reliable means for specific delivery of miRNAs to target tissues represents a major obstacle to their broad therapeutic application. Our objective was to explore the use of nucleic acid aptamers as carriers for cell-targeted delivery of a miRNA with tumor suppressor function, let-7g. Using an aptamer that binds to and antagonizes the oncogenic receptor tyrosine kinase Axl (GL21. T), here we describe the development of aptamer-miRNA conjugates as multifunctional molecules that inhibit the growth of Axl-expressing tumors. We conjugated the let-7g miRNA to GL21. T and demonstrate selective delivery to target cells, processing by the RNA interference machinery, and silencing of let-7g target genes. Importantly, the multifunctional conjugate reduced tumor growth in a xenograft model of lung adenocarcinoma. Therefore, our data establish aptamer-miRNA conjugates as a novel tool for targeted delivery of miRNAs with therapeutic potential.
引用
收藏
页码:1151 / 1163
页数:13
相关论文
共 50 条
[1]
Rational design and in vitro and in vivo delivery of Dicer substrate siRNA [J].
Amarzguioui, Mohammed ;
Lundberg, Patric ;
Cantin, Edouard ;
Hagstrom, James ;
Behlke, Mark A. ;
Rossi, John J. .
NATURE PROTOCOLS, 2006, 1 (02) :508-517
[2]
Amarzguioui Mohammed, 2008, V442, P3, DOI 10.1007/978-1-59745-191-8_1
[3]
Thermal Stability of siRNA Modulates Aptamer-conjugated siRNA Inhibition [J].
Berezhnoy, Alexey ;
Brenneman, Randall ;
Bajgelman, Marcio ;
Seales, Dawn ;
Gilboa, Eli .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2012, 1 :e51
[4]
The role of let-7 in cell differentiation and cancer [J].
Boyerinas, Benjamin ;
Park, Sun-Mi ;
Hau, Annika ;
Murmann, Andrea E. ;
Peter, Marcus E. .
ENDOCRINE-RELATED CANCER, 2010, 17 (01) :F19-F36
[5]
Understanding the nanoparticle-protein corona using methods to quantify exchange rates and affinities of proteins for nanoparticles [J].
Cedervall, Tommy ;
Lynch, Iseult ;
Lindman, Stina ;
Berggard, Tord ;
Thulin, Eva ;
Nilsson, Hanna ;
Dawson, Kenneth A. ;
Linse, Sara .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (07) :2050-2055
[6]
Targeting Axl With an High-affinity Inhibitory Aptamer [J].
Cerchia, Laura ;
Esposito, Carla L. ;
Camorani, Simona ;
Rienzo, Anna ;
Stasio, Loredana ;
Insabato, Luigi ;
Affuso, Andrea ;
de Franciscis, Vittorio .
MOLECULAR THERAPY, 2012, 20 (12) :2291-2303
[7]
Targeting cancer cells with nucleic acid aptamers [J].
Cerchia, Laura ;
de Franciscis, Vittorio .
TRENDS IN BIOTECHNOLOGY, 2010, 28 (10) :517-525
[8]
Anticancer role of MUC1 aptamer-miR-29b chimera in epithelial ovarian carcinoma cells through regulation of PTEN methylation [J].
Dai, Furong ;
Zhang, Yi ;
Zhu, Xin ;
Shan, Nianchun ;
Chen, Yuxiang .
TARGETED ONCOLOGY, 2012, 7 (04) :217-225
[9]
Systemic administration of optimized aptamer-siRNA chimeras promotes regression of PSMA-expressing tumors [J].
Dassie, Justin P. ;
Liu, Xiu-ying ;
Thomas, Gregory S. ;
Whitaker, Ryan M. ;
Thiel, Kristina W. ;
Stockdale, Katie R. ;
Meyerholz, David K. ;
McCaffrey, Anton P. ;
McNamara, James O., II ;
Giangrande, Paloma H. .
NATURE BIOTECHNOLOGY, 2009, 27 (09) :839-U95
[10]
Highly Complementary Target RNAs Promote Release of Guide RNAs from Human Argonaute2 [J].
De, Nabanita ;
Young, Lisa ;
Lau, Pick-Wei ;
Meisner, Nicole-Claudia ;
Morrissey, David V. ;
MacRae, Ian J. .
MOLECULAR CELL, 2013, 50 (03) :344-355