Targeted gene delivery of polyethyleneimine-grafted chitosan with RGD dendrimer peptide in αvβ3 integrin-overexpressing tumor cells

被引:41
作者
Kim, Young-Min [1 ]
Park, Seong-Cheol [1 ]
Jang, Mi-Kyeong [1 ]
机构
[1] Sunchon Natl Univ, Coll Engn, Dept Polymer Sci & Engn, Sunchon 57922, Jeonnam, South Korea
基金
新加坡国家研究基金会;
关键词
RGD; Chitosan; PC3; cell; Tumor-xenograft; Polyethyleneimine; DRUG-DELIVERY; THERAPY; TRANSFECTION; TRIALS;
D O I
10.1016/j.carbpol.2017.07.035
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The safe and effective delivery of genetic material into cells is a necessary factor for gene therapy. Although a wide range of materials, methods, and combinations have been reported, successful genetherapy has been limited. In the present study, a targeted gene carrier for alpha(v)beta(3) integrin-overexpressing tumor cells was designed using widely applied materials containing water soluble chitosan (WSC), RGD peptide, and polyethyleneimine (PEI). The physiological characteristics, in vitro targeted gene transfection, cytotoxicity, blood-compatibility, and cellular distributions were investigated. In particular, astudy of the endocytic mechanism revealed processes of microtubule-dependent macropinocytosis andclathrin mediated endocytosis. Furthermore, the PEI/WSC copolymer with a dendrimer RGD peptide(four-branched RGD moiety) as a targeting moiety suppressed the growth of a solid tumor mass in vivo mouse xenograft model generated with PC3 prostate tumor cells by silencing BCL2 mRNA. This result indicated RGD/PEI/WSC copolymer for a good candidate as a simple and biocompatible gene carrier. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1059 / 1068
页数:10
相关论文
共 30 条
[1]   Targeted drug delivery to tumors: Myths, reality and possibility [J].
Bae, You Han ;
Park, Kinam .
JOURNAL OF CONTROLLED RELEASE, 2011, 153 (03) :198-205
[2]   Targeting tumor stroma and exploiting mature tumor vasculature to improve anti-cancer drug delivery [J].
Bouzin, Caroline ;
Feron, Olivier .
DRUG RESISTANCE UPDATES, 2007, 10 (03) :109-120
[3]  
Cabodi S., 2010, NATURE REV CANC
[4]   Chitosan: An Update on Potential Biomedical and Pharmaceutical Applications [J].
Cheung, Randy Chi Fai ;
Ng, Tzi Bun ;
Wong, Jack Ho ;
Chan, Wai Yee .
MARINE DRUGS, 2015, 13 (08) :5156-5186
[5]   αv integrins regulate cell proliferation through integrin-linked kinase (ILK) in ovarian cancer cells [J].
Cruet-Hennequart, S ;
Maubant, S ;
Luis, J ;
Gauduchon, P ;
Staedel, C ;
Dedhar, S .
ONCOGENE, 2003, 22 (11) :1688-1702
[6]   Linear PEI nanoparticles: efficient pDNA/siRNA carriers in vitro and in vivo [J].
Goyal, Ritu ;
Tripathi, Sushil K. ;
Tyagi, Shilpa ;
Sharma, Anurag ;
Ram, K. Ravi ;
Chowdhuri, Debapratim K. ;
Shukla, Yogeshwar ;
Kumar, P. ;
Gupta, Kailash C. .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2012, 8 (02) :167-175
[7]   Cytotoxic Impacts of Linear and Branched Polyethylenimine Nanostructures in A431 Cells [J].
Kafil, Vala ;
Omidi, Yadollah .
BIOIMPACTS, 2011, 1 (01) :23-30
[8]  
Katare DP., 2010, I.J.T.P.R, V1, P33
[9]   Synergistic nanomedicine by combined gene and photothermal therapy [J].
Kim, Jinhwan ;
Kim, Jihoon ;
Jeong, Cherlhyun ;
Kim, Won Jong .
ADVANCED DRUG DELIVERY REVIEWS, 2016, 98 :99-112
[10]   Transfection and intracellular trafficking properties of carbon dot-gold nanoparticle molecular assembly conjugated with PEI-pDNA [J].
Kim, Jinhwan ;
Park, Juhee ;
Kim, Hyunwoo ;
Singha, Kaushik ;
Kim, Won Jong .
BIOMATERIALS, 2013, 34 (29) :7168-7180