Molecular imaging of gene therapy for cancer

被引:127
作者
Shah, K
Jacobs, A
Breakefield, XO
Weissleder, R
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Mol Imaging Res, Boston, MA USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol,Neurosci Program,Mol Neurogenet Unit, Boston, MA USA
[3] Max Planck Inst Neurol Res, Dept Neurol, Lab Gene Therapy & Mol Imaging, Cologne, Germany
[4] CMMC, Cologne, Germany
关键词
MRI; virus vectors; bioluminescence; PET; FIAU; fluorescence;
D O I
10.1038/sj.gt.3302278
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene therapy of cancer has been one of the most exciting and elusive areas of scientific and clinical research in the past decade. One of the most critical issues for ensuring success of this therapy is the development of technology for noninvasive monitoring of the location, magnitude and duration of vector-mediated gene expression, as well as the distribution and targeting of vector particles in vivo. In recent years many advances have been made in high-resolution, in vivo imaging methods, including: radionuclide imaging, such as positron emission tomography ( PET) and single photon emission tomography ( SPECT), magnetic resonance (MR) imaging and spectroscopy, bioluminescence imaging and various fluorescence imaging techniques, including fluorescence-mediated tomography (FMT) and near-infrared fluorescence (NIRF) reflectance imaging. A variety of factors determine the choice of specific imaging system, some of them are the imaging requirements ( single or repeated), intended use ( animal or human) and spatial requirements ( organs versus cellular resolution and depth). This review provides descriptions of modalities applicable to imaging different parameters of vector-mediated gene expression in tumors and stem cell tracking in vivo.
引用
收藏
页码:1175 / 1187
页数:13
相关论文
共 92 条
  • [1] Neural stem cells display extensive tropism for pathology in adult brain: Evidence from intracranial gliomas
    Aboody, KS
    Brown, A
    Rainov, NG
    Bower, KA
    Liu, SX
    Yang, W
    Small, JE
    Herrlinger, U
    Ourednik, V
    Black, PM
    Breakefield, XO
    Snyder, EY
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) : 12846 - 12851
  • [2] In vivo imaging of gene and cell therapies
    Allport, JR
    Weissleder, R
    [J]. EXPERIMENTAL HEMATOLOGY, 2001, 29 (11) : 1237 - 1246
  • [3] Receptor-targeted optical imaging of tumors with near-infrared fluorescent ligands
    Becker, A
    Hessenius, C
    Licha, K
    Ebert, B
    Sukowski, U
    Semmler, W
    Wiedenmann, B
    Grötzinger, C
    [J]. NATURE BIOTECHNOLOGY, 2001, 19 (04) : 327 - 331
  • [4] Optical imaging of Renilla luciferase reporter gene expression in living mice
    Bhaumik, S
    Gambhir, SS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) : 377 - 382
  • [5] Blackstock AW, 2001, CLIN CANCER RES, V7, P3263
  • [6] Blasberg RG, 1999, Q J NUCL MED, V43, P163
  • [7] The development of in vivo imaging systems to study gene expression
    Bogdanov, A
    Weissleder, R
    [J]. TRENDS IN BIOTECHNOLOGY, 1998, 16 (01) : 5 - 10
  • [8] Approaches and agents for imaging the vascular system
    Bogdanov, AA
    Lewin, M
    Weissleder, R
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 1999, 37 (1-3) : 279 - 293
  • [9] Bogdanov AA, 2000, Q J NUCL MED, V44, P224
  • [10] In vivo imaging of gene delivery and expression
    Bogdanov, Alexei, Jr.
    Weissleder, Ralph
    [J]. TRENDS IN BIOTECHNOLOGY, 2002, 20 (08) : S11 - S18