Tumor-Targeted Drug Delivery with Aptamers

被引:94
作者
Zhang, Y. [2 ]
Hong, H. [1 ]
Cai, W. [1 ,2 ,3 ]
机构
[1] Univ Wisconsin, Dept Radiol, Sch Med & Publ Hlth, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Med Phys, Sch Med & Publ Hlth, Madison, WI 53705 USA
[3] Univ Wisconsin Carbone Canc Ctr, Madison, WI USA
关键词
Aptamers; drug delivery; cancer; nanomedicine; theranostics; RNA interference; siRNA; ASPARTYL CHLORIN E(6); PROSTATE-CANCER CELLS; IN-VIVO; QUANTUM DOTS; CHEMICAL BIOLOGY; RNA MOLECULES; HIGH-AFFINITY; DOXORUBICIN; GROWTH; SIRNA;
D O I
10.2174/092986711797189547
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer is one of the leading causes of death around the world. Tumor-targeted drug delivery is one of the major areas in cancer research. Aptamers exhibit many desirable properties for tumor-targeted drug delivery, such as ease of selection and synthesis, high binding affinity and specificity, low immunogenicity, and versatile synthetic accessibility. Over the last several years, aptamers have quickly become a new class of targeting ligands for drug delivery applications. In this review, we will discuss in detail about aptamer-based delivery of chemotherapy drugs (e. g. doxorubicin, docetaxel, daunorubicin, and cisplatin), toxins (e. g. gelonin and various photodynamic therapy agents), and a variety of small interfering RNAs. Although the results are promising which warrants enthusiasm for aptamer-based drug delivery, tumor homing of aptamer-based conjugates after systemic injection has only been achieved in one report. Much remains to be done before aptamer-based drug delivery can reach clinical trials and eventually the day-to-day management of cancer patients. Therefore, future directions and challenges in aptamer-based drug delivery are also discussed.
引用
收藏
页码:4185 / 4194
页数:10
相关论文
共 103 条
[1]   Maximizing the delivery of intraperitoneal therapy while minimizing drug toxicity and maintaining quality of life [J].
Alberts, David S. ;
Delforge, Ardie .
SEMINARS IN ONCOLOGY, 2006, 33 (06) :S8-S17
[2]  
[Anonymous], J BIOMATER SCI POLYM
[3]   Quantum dot - Aptamer conjugates for synchronous cancer imaging, therapy, and sensing of drug delivery based on Bi-fluorescence resonance energy transfer [J].
Bagalkot, Vaishali ;
Zhang, Liangfang ;
Levy-Nissenbaum, Etgar ;
Jon, Sangyong ;
Kantoff, Philip W. ;
Langer, Robert ;
Farokhzad, Omid C. .
NANO LETTERS, 2007, 7 (10) :3065-3070
[4]   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
[5]   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
[6]  
Blagosklonny MV, 2004, CELL CYCLE, V3, P1035
[7]   Phase I dose escalation trial of weekly docetaxel plus irinotecan in patients with advanced cancer [J].
Bleickardt, E ;
Argiris, A ;
Rich, R ;
Blum, K ;
McKeon, A ;
Tara, H ;
Zelterman, D ;
Burtness, B ;
Davies, MJ ;
Murren, JR .
CANCER BIOLOGY & THERAPY, 2002, 1 (06) :646-651
[8]   Peptide-labeled near-infrared quantum dots for imaging tumor vasculature in living subjects [J].
Cai, WB ;
Shin, DW ;
Chen, K ;
Gheysens, O ;
Cao, QZ ;
Wang, SX ;
Gambhir, SS ;
Chen, XY .
NANO LETTERS, 2006, 6 (04) :669-676
[9]   Multimodality molecular imaging of tumor angiogenesis [J].
Cai, Weibo ;
Chen, Xiaoyuan .
JOURNAL OF NUCLEAR MEDICINE, 2008, 49 :113S-128S
[10]   Dual-function probe for PET and near-infrared fluorescence imaging of tumor vasculature [J].
Cai, Weibo ;
Chen, Kai ;
Li, Zi-Bo ;
Gambhir, Sanjiv S. ;
Chen, Xiaoyuan .
JOURNAL OF NUCLEAR MEDICINE, 2007, 48 (11) :1862-1870