PEG-PBLG nanoparticle-mediated HSV-TK/GCV gene therapy for oral squamous cell carcinoma

被引:25
|
作者
Yyu, Dongsheng [1 ]
Wang, Anxun [2 ]
Huang, Hongzhang [1 ]
Chen, Yiyang [1 ]
机构
[1] Sun Yat Sen Univ, Dept Oral & Maxillofacial Surg, Guanghua Coll Stomatol, Guangzhou 510055, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Oral & Maxillofacial Surg, Guangzhou 510080, Guangdong, Peoples R China
关键词
ganciclovir; gene therapy; golden hamster; herpes simplex virus thymidine kinase; nanoparticles; oral squamous cell carcinoma; poly-gamma-benzyl-L-glutamate; polyethylene-glycol;
D O I
10.2217/17435889.3.6.813
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: Previous studies revealed that drug-loaded poly(ethylene-glycol)-poly(gamma-benzyl-L-glutamate) (PEG-PBLG) nanoparticles exhibit favorable pharmacokinetic characteristics in the treatment of oral squamous cell carcinoma (OSCC). In this study, the characteristics and anticancer effect of herpes simplex virus thymidine kinase (HSV-TK)-loaded PEG-PBLG nanoparticles for OSCC were investigated. Materials & methods: HSV-TK-loaded PEG-PBLG nanoparticles were prepared and their morphology, DNA protection and gene-transfer efficiency were evaluated. Their anticancer effect in vitro and in vivo was determined. Results & discussion: HSV-TK-loaded PEG-PBLG nanoparticles have a core-shell structure and DNA protection and higher genetransfer efficiency. PEG-PBLG nanoparticle-mediated HSV-TK/ganciclovir(GCV) had a strong anticancer effect on Tca8113 cells in vitro and buccal carcinoma induced in golden hamsters. Conclusion: PEG-PBLG nanoparticles may be a superior gene carrier in future clinical applications because of their DNA protection and higher gene-transfer efficiency. The HSV-TK/GCV suicide-gene system had significant antitumor effects on OSCC.
引用
收藏
页码:813 / 821
页数:9
相关论文
共 50 条
  • [21] Enhanced therapeutic effect of multiple injections of HSV-TK plus GCV gene therapy in combination with ionizing radiation in a mouse mammary tumor model
    Vlachaki, MT
    Chhikara, M
    Aguilar, L
    Zhu, XH
    Chiu, KJ
    Woo, S
    Teh, BS
    Thompson, TC
    Butler, EB
    Aguilar-Cordova, E
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 51 (04): : 1008 - 1017
  • [22] Influence of p53 status on the HSV-Tk/GCV-induced bystander effect in a panel of human ovarian carcinoma cell lines
    van Dillen, IJ
    Mulder, NH
    Sluiter, WJ
    Meijer, C
    de Jong, S
    Loncarek, J
    Mesnil, M
    de Vries, EFJ
    Vaalburg, W
    Hospers, GAP
    ONCOLOGY RESEARCH, 2005, 15 (03) : 151 - 159
  • [23] An experimental study on cervix cancer with combination of HSV-TK/GCV suicide gene therapy system and 60Co radiotherapy
    Chen, Daozhen
    Tang, Qiusha
    BMC CANCER, 2010, 10
  • [24] Gene Therapy of HSV-TK Transferred by the EBV based Expression Vector on Experimental Hepatocellular Carcinoma
    丁庆庆
    吴在德
    陈孝平
    胡俊波
    詹永强
    Journal of Tongji Medical University, 2001, (02) : 122 - 125
  • [25] Gene therapy of HSV-TK transferred by the EBV based expression vector on experimental hepatocellular carcinoma
    Ding Qingqing
    Wu Zaide
    Chen Xiaoping
    Abdelwahab H. M. Musa
    Hu Junbo
    Zhan Yongqiang
    Current Medical Science, 2001, 21 : 122 - 125
  • [26] Real-Time Visualizing and Tracing of HSV-TK/GCV Suicide Gene Therapy by Near-Infrared Fluorescent Quantum Dots
    Shao, Dan
    Li, Jing
    Xiao, Xuanang
    Zhang, Ming
    Pan, Yue
    Li, Shuo
    Wang, Zheng
    Zhang, Xin
    Zheng, Huilin
    Zhang, Xuewen
    Chen, Li
    ACS APPLIED MATERIALS & INTERFACES, 2014, 6 (14) : 11082 - 11090
  • [27] Side populations of glioblastoma cells are less sensitive to HSV-TK/GCV suicide gene therapy system than the non-side population
    Weiwei Hu
    Weiguo Liu
    In Vitro Cellular & Developmental Biology - Animal, 2010, 46 : 497 - 501
  • [28] Side populations of glioblastoma cells are less sensitive to HSV-TK/GCV suicide gene therapy system than the non-side population
    Hu, Weiwei
    Liu, Weiguo
    IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2010, 46 (06) : 497 - 501
  • [29] New drug delivery system for water-soluble drugs using silicone and its usefulness for local treatment: application of GCV-silicone to GCV/HSV-tk gene therapy for brain tumor
    Maeda, M
    Moriuchi, S
    Sano, A
    Yoshimine, T
    JOURNAL OF CONTROLLED RELEASE, 2002, 84 (1-2) : 15 - 25
  • [30] Gene therapy for the treatment of oral squamous cell carcinoma
    Xi, S
    Grandis, JR
    JOURNAL OF DENTAL RESEARCH, 2003, 82 (01) : 11 - 16