Precise glioblastoma targeting by AS1411 aptamer-functionalized poly (L-γ-glutamylglutamine)-paclitaxel nanoconjugates

被引:58
作者
Luo, Zimiao [1 ]
Yan, Zhiqiang [1 ]
Jin, Kai [2 ]
Pang, Qiang [2 ]
Jiang, Ting [2 ]
Lu, Heng [2 ]
Liu, Xianping [2 ]
Pang, Zhiqing [2 ]
Yu, Lei [1 ]
Jiang, Xinguo [2 ]
机构
[1] East China Normal Univ, Biomed Engn & Technol Inst, Shanghai Engn Res Ctr Mol Therapeut & New Drug De, Sch Chem & Mol Engn, 3663 N Zhongshan Rd, Shanghai 200062, Peoples R China
[2] Fudan Univ, Dept Pharmaceut, Key Lab Smart Drug Delivery, Minist Educ & PLA,Sch Pharm, 826 N Zhangheng Rd, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
Glioblastoma; Aptamer; Nucleolin; Paclitaxel-nanoconjugate; Targeting drug delivery system; DRUG-DELIVERY; MALIGNANT GLIOMA; CELL-SURFACE; PHASE-II; PACLITAXEL; NUCLEOLIN; NANOPARTICLES; THERAPY; TUMORS; CHALLENGES;
D O I
10.1016/j.jcis.2016.12.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Chemotherapy is still the main adjuvant strategy after surgery in glioblastoma therapy. As the main obstacles of chemotherapeutic drugs for glioblastoma treatment, the blood brain barrier (BBB) and non-specific delivery to non-tumor tissues greatly limit the accumulation of drugs into tumor tissues and simultaneously cause serious toxicity to nearby normal tissues which altogether compromised the chemotherapeutic effect. In the present study, we established an aptamer AS1411-functionalized poly (L-gamma-glutamyl-glutamine)-paclitaxel (PGG-PTX) nanoconjugates drug delivery system (AS1411-PGG-PTX), providing an advantageous solution of combining the precisely active targeting and the optimized solubilization of paclitaxel. The receptor nucleolin, highly expressed in glioblastoma 087 MG cells as well as neo-vascular endothelial cells, mediated the binding and endocytosis of AS1411-PGG-PTX nanoconjugates, leading to significantly enhanced uptake of AS1411-PGG-PTX nanoconjugates by tumor cells and three-dimension tumor spheroids, and intensive pro-apoptosis effect of AS1411-PGG-PTX nanoconjugates. In vivo fluorescence imaging and tissue distribution further demonstrated the higher tumor distribution of AS1411-PGG-PTX as compared with PGG-PTX. As a result, the AS1411-PGG-PTX nanoconjugates d presented the best anti-glioblastoma effect with prolonged median survival time and most tumor cell apoptosis in vivo as compared with other groups. In conclusion, the AS1411-PGG-PTX nanoconjugates exhibited a promising targeting delivery strategy for glioblastoma therapy. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:783 / 796
页数:14
相关论文
共 50 条
[1]   RNA-binding protein nucleolin in disease [J].
Abdelmohsen, Kotb ;
Gorospe, Myriam .
RNA BIOLOGY, 2012, 9 (06) :799-808
[2]   Delivery of molecularly targeted therapy to malignant glioma, a disease of the whole brain [J].
Agarwal, Sagar ;
Sane, Ramola ;
Oberoi, Rajneet ;
Ohlfest, John R. ;
Elmquist, William F. .
EXPERT REVIEWS IN MOLECULAR MEDICINE, 2011, 13 :e17
[3]   Aptamer-conjugated polymeric nanoparticles for targeted cancer therapy [J].
Aravind, Athulya ;
Yoshida, Yasuhiko ;
Maekawa, Toru ;
Kumar, D. Sakthi .
DRUG DELIVERY AND TRANSLATIONAL RESEARCH, 2012, 2 (06) :418-436
[4]   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
[5]   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
[6]   Development of aptamer therapeutics [J].
Bunka, David H. J. ;
Platonova, Olga ;
Stockley, Peter G. .
CURRENT OPINION IN PHARMACOLOGY, 2010, 10 (05) :557-562
[7]   Active targeting schemes for nanoparticle systems in cancer therapeutics [J].
Byrne, James D. ;
Betancourt, Tania ;
Brannon-Peppas, Lisa .
ADVANCED DRUG DELIVERY REVIEWS, 2008, 60 (15) :1615-1626
[8]   Nucleolin expressed at the cell surface is a marker of endothelial cells in angiogenic blood vessels [J].
Christian, S ;
Pilch, J ;
Akerman, ME ;
Porkka, K ;
Laakkonen, P ;
Ruoslahti, E .
JOURNAL OF CELL BIOLOGY, 2003, 163 (04) :871-878
[9]  
de Lange ECM, 2012, CURR PHARM BIOTECHNO, V13, P2319
[10]   Cell surface nucleolin antagonist causes endothelial cell apoptosis and normalization of tumor vasculature [J].
Fogal, Valentina ;
Sugahara, Kazuki N. ;
Ruoslahti, Erkki ;
Christian, Sven .
ANGIOGENESIS, 2009, 12 (01) :91-100