Targeting cancer cells with nucleic acid aptamers

被引:215
作者
Cerchia, Laura [1 ]
de Franciscis, Vittorio [1 ]
机构
[1] CNR G Salvatore, Ist Endocrinol & Oncol Sperimentale, I-80131 Naples, Italy
关键词
ACUTE MYELOID-LEUKEMIA; SYSTEMATIC EVOLUTION; DNA APTAMERS; TUMOR-CELLS; IN-VIVO; EXPONENTIAL ENRICHMENT; MOLECULAR RECOGNITION; SIRNA CHIMERAS; DRUG-DELIVERY; RNA MOLECULES;
D O I
10.1016/j.tibtech.2010.07.005
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
Aptamers are short, structured, single-stranded RNA or DNA ligands that bind with high affinity to their target molecules, which range from small chemicals to large cell-surface and transmembrane proteins. Aptamers are now emerging as promising molecules to target specific cancer epitopes in clinical diagnosis and therapy. Furthermore, because of their high specificity and low toxicity, aptamers might be considered as the compounds-of-choice for in vivo cell recognition. Specific cancer cell recognition could be capitalized upon for delivering therapeutic nanoparticles, small interfering RNA bioconjugates, chemotherapeutic cargos or molecular imaging probes. In this article, we review recent advances in the use of aptamers for in vivo cancer cell recognition, with a particular focus on novel applications of aptamers for targeting the cell surface.
引用
收藏
页码:517 / 525
页数:9
相关论文
共 70 条
[1]
Ashworth T.R., 1869, Australas Med J, V14, P146
[2]
An aptamer-doxorubicin physical conjugate as a novel targeted drug-delivery platform [J].
Bagalkot, Vaishali ;
Farokhzad, Omid C. ;
Langer, Robert ;
Jon, Sangyong .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (48) :8149-8152
[3]
Discovery and development of the G-rich oligonucleotide AS1411 as a novel treatment for cancer [J].
Bates, Paula J. ;
Laber, Damian A. ;
Miller, Donald M. ;
Thomas, Shelia D. ;
Trent, John O. .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2009, 86 (03) :151-164
[4]
Antiproliferative activity of G-rich oligonucleotides correlates with protein binding [J].
Bates, PJ ;
Kahlon, JB ;
Thomas, SD ;
Trent, JO ;
Miller, DM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) :26369-26377
[5]
Systematic evolution of a DNA aptamer binding to rat brain tumor microvessels - Selective targeting of endothelial regulatory protein pigpen [J].
Blank, M ;
Weinschenk, T ;
Priemer, M ;
Schluesener, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (19) :16464-16468
[6]
Design and synthesis of mono- and multimeric targeted radiopharmaceuticals based on novel cyclen ligands coupled to Anti-MUC1 aptamers for the diagnostic imaging and targeted radiotherapy of cancer [J].
Borbas, K. Eszter ;
Ferreira, Catia S. M. ;
Perkins, Alan ;
Bruce, James I. ;
Missailidis, Sotiris .
BIOCONJUGATE CHEMISTRY, 2007, 18 (04) :1205-1212
[7]
Discovery and Development of Therapeutic Aptamers [J].
Bouchard, P. R. ;
Hutabarat, R. M. ;
Thompson, K. M. .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2010, 50 :237-257
[8]
RETRACTED: Neutralizing aptamers from whole-cell SELEX inhibit the RET receptor tyrosine kinase (Retracted Article) [J].
Cerchia, L ;
Ducongé, F ;
Pestourie, C ;
Boulay, J ;
Aissouni, Y ;
Gombert, K ;
Tavitian, B ;
de Franciscis, V ;
Libri, D .
PLOS BIOLOGY, 2005, 3 (04) :697-704
[9]
RETRACTED: Differential SELEX in Human Glioma Cell Lines (Retracted Article) [J].
Cerchia, Laura ;
Esposito, Carla Lucia ;
Jacobs, Andreas H. ;
Tavitian, Bertrand ;
de Franciscis, Vittorio .
PLOS ONE, 2009, 4 (11)
[10]
Cerchia Laura, 2009, V535, P59, DOI 10.1007/978-1-59745-557-2_5