Smart Polymeric Nanoparticles for Cancer Gene Delivery

被引:126
作者
Lin, Guimei [1 ]
Zhang, Hong [1 ,2 ,3 ]
Huang, Leaf
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China
[2] Univ N Carolina, Eshelman Sch Pharm, Div Mol Pharmaceut, Chapel Hill, NC 27599 USA
[3] Yuxi Municipal Hosp Tradit Chinese Med, Yuxi 653100, Peoples R China
基金
中国国家自然科学基金;
关键词
gene delivery; cancer therapy; nanoparticle; CHITOSAN-GRAFT-POLYETHYLENIMINE; MESOPOROUS SILICA NANOPARTICLES; IRON-OXIDE NANOPARTICLES; TARGETED CO-DELIVERY; DRUG-DELIVERY; IN-VIVO; SIRNA DELIVERY; BREAST-CANCER; MULTIFUNCTIONAL NANOPARTICLES; SURFACE MODIFICATION;
D O I
10.1021/mp500656v
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The massive amount of human genetic information already available has accelerated the identification of target genes, making gene and nucleic acid therapy the next generation of medicine. Nanoparticle (NP)-based anticancer gene therapy treatment has received significant interest in this evolving field. Recent advances in vector technology have improved gene transfection efficiencies of nonviral vectors to a level similar to viruses. This review serves as an introduction to surface modifications of NPs based on polymeric structural improvements and target moieties. A discussion regarding the future perspective of multifunctional NPs in cancer therapy is also included.
引用
收藏
页码:314 / 321
页数:8
相关论文
共 85 条
[51]   Progress in developing cationic vectors for non-viral systemic gene therapy against cancer [J].
Morille, Marie ;
Passirani, Catherine ;
Vonarbourg, Arnaud ;
Clavreul, Anne ;
Benoit, Jean-Pierre .
BIOMATERIALS, 2008, 29 (24-25) :3477-3496
[52]   THE BASIC SCIENCE OF GENE-THERAPY [J].
MULLIGAN, RC .
SCIENCE, 1993, 260 (5110) :926-932
[53]   Aliphatic Lipid Substitution on 2 kDa Polyethylenimine Improves Plasmid Delivery and Transgene Expression [J].
Neamnark, Artphop ;
Suwantong, Orawan ;
Bahadur, Remant K. C. ;
Hsu, Charlie Y. M. ;
Supaphol, Pitt ;
Uludag, Hasan .
MOLECULAR PHARMACEUTICS, 2009, 6 (06) :1798-1815
[54]   Nanotoxicology:: An emerging discipline evolving from studies of ultrafine particles [J].
Oberdörster, G ;
Oberdörster, E ;
Oberdörster, J .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2005, 113 (07) :823-839
[55]   Influence of targeting ligand flexibility on receptor binding of particulate drug delivery systems [J].
Olivier, V ;
Meisen, I ;
Meckelein, B ;
Hirst, TR ;
Peter-Katalinic, J ;
Schmidt, MA ;
Frey, A .
BIOCONJUGATE CHEMISTRY, 2003, 14 (06) :1203-1208
[56]   Current status of polymeric gene delivery systems [J].
Park, Tae Gwan ;
Jeong, Ji Hoon ;
Kim, Sung Wan .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (04) :467-486
[57]   Toward theragnostics [J].
Pene, Frederic ;
Courtine, Emilie ;
Cariou, Alain ;
Mira, Jean-Paul .
CRITICAL CARE MEDICINE, 2009, 37 (01) :S50-S58
[58]   Epidermal Stem Cells Manipulated by pDNA-VEGF165/CYD-PEI Nanoparticles Loaded Gelatin/β-TCP Matrix as a Therapeutic Agent and Gene Delivery Vehicle for Wound Healing [J].
Peng, Li-Hua ;
Wei, Wei ;
Qi, Xiao-Tian ;
Shan, Ying-Hui ;
Zhang, Fang-Jun ;
Chen, Xi ;
Zhu, Qian-Ying ;
Yu, Lian ;
Liang, Wen-Quan ;
Gao, Jian-Qing .
MOLECULAR PHARMACEUTICS, 2013, 10 (08) :3090-3102
[59]  
PEREY L, 1992, CANCER RES, V52, P2563
[60]   Anti-apoptosis and cell survival: A review [J].
Portt, Liam ;
Norman, Grant ;
Clapp, Caitlin ;
Greenwood, Matthew ;
Greenwood, Michael T. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2011, 1813 (01) :238-259