Molecular imaging of biological gene delivery vehicles for targeted cancer therapy: Beyond viral vectors

被引:9
|
作者
Min J.-J. [1 ]
Nguyen V.H. [1 ]
Gambhir S.S. [2 ]
机构
[1] Department of Nuclear Medicine, Chonnam National University Medical School, Dong-gu, Gwangju 501-746
[2] Molecular Imaging Program, Department of Radiology and Bioengineering, Bio-X Program, Stanford University, Stanford
基金
新加坡国家研究基金会;
关键词
Cancer; Gene delivery vector; Gene therapy; Molecular imaging;
D O I
10.1007/s13139-009-0006-3
中图分类号
学科分类号
摘要
Cancer persists as one of the most devastating diseases in the world. Problems including metastasis and tumor resistance to chemotherapy and radiotherapy have seriously limited the therapeutic effects of present clinical treatments. To overcome these limitations, cancer gene therapy has been developed over the last two decades for a broad spectrum of applications, from gene replacement and knockdown to vaccination, each with different requirements for gene delivery. So far, a number of genes and delivery vectors have been investigated, and significant progress has been made with several gene therapy modalities in clinical trials. Viral vectors and synthetic liposomes have emerged as the vehicles of choice for many applications. However, both have limitations and risks that restrict gene therapy applications, including the complexity of production, limited packaging capacity, and unfavorable immunological features. While continuing to improve these vectors, it is important to investigate other options, particularly nonviral biological agents such as bacteria, bacteriophages, and bacteria-like particles. Recently, many molecular imaging techniques for safe, repeated, and high-resolution in vivo imaging of gene expression have been employed to assess vector-mediated gene expression in living subjects. In this review, molecular imaging techniques for monitoring biological gene delivery vehicles are described, and the specific use of these methods at different steps is illustrated. Linking molecular imaging to gene therapy will eventually help to develop novel gene delivery vehicles for preclinical study and support the development of future human applications. © Korean Society of Nuclear Medicine 2010.
引用
收藏
页码:15 / 24
页数:9
相关论文
共 50 条
  • [31] Engineering Viral Vectors for Acoustically Targeted Gene Delivery to the Brain across Species
    Li, Hongyi Richard
    Szablowski, Jerzy
    Shapiro, Mikhail
    MOLECULAR THERAPY, 2024, 32 (04) : 65 - 66
  • [32] Targeted vectors for gene therapy of cancer and retroviral infections
    Walther, W
    Stein, U
    MOLECULAR BIOTECHNOLOGY, 1996, 6 (03) : 267 - 286
  • [33] Targeted adenoviral vectors for cancer gene therapy (Review)
    Douglas, JT
    Curiel, DT
    INTERNATIONAL JOURNAL OF ONCOLOGY, 1997, 11 (02) : 341 - 348
  • [34] Delivery systems intended for in vivo gene therapy of cancer: targeting and replication competent viral vectors
    Galanis, E
    Vile, R
    Russell, SJ
    CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2001, 38 (03) : 177 - 192
  • [35] Aerosol gene delivery using viral vectors and cationic carriers for in vivo lung cancer therapy
    Hong, Seong-Ho
    Park, Sung-Jin
    Lee, Somin
    Cho, Chong Su
    Cho, Myung-Haing
    EXPERT OPINION ON DRUG DELIVERY, 2015, 12 (06) : 977 - 991
  • [36] Optimal delivery of RNA interference by viral vectors for cancer therapy
    Wong, Boaz
    Birtch, Rayanna
    Rezaei, Reza
    Jamieson, Taylor
    Crupi, Mathieu J. F.
    Diallo, Jean-Simon
    Ilkow, Carolina S.
    MOLECULAR THERAPY, 2023, 31 (11) : 3127 - 3145
  • [37] Viral vectors for cancer gene therapy: Viral dissemination and tumor targeting
    Jia, W
    Zhou, Q
    CURRENT GENE THERAPY, 2005, 5 (01) : 133 - 142
  • [38] Gene therapy with viral vectors
    Kootstra, NA
    Verma, IM
    ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2003, 43 : 413 - 439
  • [39] Viral vectors in gene therapy
    Slade, N
    PERIODICUM BIOLOGORUM, 2001, 103 (02) : 139 - 143
  • [40] Viral vectors for gene therapy
    Robbins, PD
    Tahara, H
    Ghivizzani, SC
    TRENDS IN BIOTECHNOLOGY, 1998, 16 (01) : 35 - 40