Targeting prostate cancer cells with genetically engineered polypeptide-based micelles displaying gastrin-releasing peptide

被引:25
|
作者
Zhang, Wei [1 ,2 ]
Garg, Sanjay [1 ,2 ]
Eldi, Preethi [1 ,2 ]
Zhou, Fiona Huan-huan [3 ]
Johnson, Ian R. D. [1 ,2 ]
Brooks, Doug A. [1 ,2 ]
Lam, Frankie [1 ,2 ]
Rychkov, Grigori [3 ]
Hayball, John [1 ,2 ]
Albrecht, Hugo [1 ,2 ]
机构
[1] Univ South Australia, Sansom Inst Hlth Res, Ctr Drug Discovery & Dev, Ctr Pharmaceut Innovat & Dev, Adelaide, SA 5001, Australia
[2] Univ South Australia, Sch Pharm & Med Sci, Adelaide, SA 5001, Australia
[3] SAHMRI, North Terrace, Adelaide, SA 5001, Australia
关键词
G protein-coupled receptors (GPCRs); Elastin-like polypeptide (ELP); Gastrin releasing peptide (GRP); Micelle; Prostate cancer; ELASTIN-LIKE POLYPEPTIDES; DRUG; NANOPARTICLES; PROTEIN; DELIVERY; INDUCTION; APOPTOSIS; VEHICLES; RECEPTOR; LIGANDS;
D O I
10.1016/j.ijpharm.2016.09.039
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years G protein-coupled receptors (GPCRs) have emerged as crucial tumorigenic factors that drive aberrant cancer growth, metastasis and angiogenesis. Consequently, a number of GPCRs are strongly expressed in cancer derived cell lines and tissue samples. Therefore a rational anti-cancer strategy is the design of nano-medicines that specifically target GPCRs to bind and internalise cytotoxic drugs into cancer cells. Herein, we report the genetic engineering of a self-assembling nanoparticle based on elastin-like polypeptide (ELP), which has been fused with gastrin releasing peptide (GRP). These nanoparticles increased intracellular calcium concentrations when added to GRP receptor positive PC-3 prostate cancer cells, demonstrating specific receptor activation. Moreover, GRP-displaying fluorescent labelled nanoparticles showed specific cell-surface interaction with PC-3 prostate cancer cells and increased endocytic uptake. These nanoparticles therefore provide a targeted molecular carrier system for evaluating the delivery of cytotoxic drugs into cancer cells. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:270 / 279
页数:10
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