DNA and RNA aptamers: From tools for basic research towards therapeutic applications

被引:75
作者
Ulrich, Henning [1 ]
Trujillo, Cleber A.
Nery, Arthur A.
Alves, Janaina M.
Majumder, Paromita
Resende, Rodrigo R.
Martins, Antonio H.
机构
[1] Univ Sao Paulo, Inst Quim, Dept Bioquim, BR-05508900 Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, Dept Neurociencias, BR-0402362 Sao Paulo, Brazil
关键词
SELEX; aptamer; therapeutic agent; high-throughput screening;
D O I
10.2174/138620706778249695
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The systematic evolution of ligands by exponential enrichment (SELEX) is a combinatorial oligonucleotide library-based in vitro selection approach in which DNA or RNA molecules are selected by their ability to bind their targets with high affinity and specificity, comparable to those of antibodies. Nucleic acids with high affinity for their targets have been selected against a wide variety of compounds, from small molecules, such as ATP, to membrane proteins and even whole organisms. Recently, the use of the SELEX technique was extended to isolate oligonucleotide ligands, also known as aptamers, for a wide range of proteins of importance for therapy and diagnostics, such as growth factors and cell surface antigens. The number of aptamers generated as inhibitors of various target proteins has increased following automatization of the SELEX process. Their diagnostic and therapeutic efficacy can be enhanced by introducing chemical modifications into the oligonucleotides to provide resistance against enzymatic degradation in body fluids. Several aptamers are currently being tested in preclinical and clinical trials, and aptamers are in the process of becoming a new class of therapeutic agents. Recently, the anti-VEGF aptamer pegaptanib received FDA approval for treatment of human ocular vascular disease.
引用
收藏
页码:619 / 632
页数:14
相关论文
共 126 条
[81]   VASCULAR ENDOTHELIAL GROWTH-FACTOR VASCULAR-PERMEABILITY FACTOR EXPRESSION IN A MOUSE MODEL OF RETINAL NEOVASCULARIZATION [J].
PIERCE, EA ;
AVERY, RL ;
FOLEY, ED ;
AIELLO, LP ;
SMITH, LEH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (03) :905-909
[82]  
Pietras K, 2001, CANCER RES, V61, P2929
[83]  
PRABHAVATHI BF, 1998, CURR OPIN CHEM BIOL, V2, P567
[84]   Aptamers - basic research, drug development, and clinical applications [J].
Proske, D ;
Blank, M ;
Buhmann, R ;
Resch, A .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2005, 69 (04) :367-374
[85]  
Proske D, 2002, CHEMBIOCHEM, V3, P717, DOI 10.1002/1439-7633(20020802)3:8<717::AID-CBIC717>3.0.CO
[86]  
2-C
[87]  
Rajendran M, 2002, COMB CHEM HIGH T SCR, V5, P263
[88]   The generation and characterization of antagonist RNA aptamers to human oncostatin M [J].
Rhodes, A ;
Deakin, A ;
Spaull, J ;
Coomber, B ;
Aitken, A ;
Life, P ;
Rees, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (37) :28555-28561
[89]   Nucleic acid aptamers as tools and drugs: Recent developments [J].
Rimmele, M .
CHEMBIOCHEM, 2003, 4 (10) :963-971
[90]   Interfering with hepatitis C virus IRES activity using RNA molecules identified by a novel in vitro selection method [J].
Romero-López, C ;
Barroso-delJesus, A ;
Puerta-Fernández, E ;
Berzal-Herranz, A .
BIOLOGICAL CHEMISTRY, 2005, 386 (02) :183-190