Advances in imaging mouse tumour models in vivo

被引:134
作者
Lyons, SK [1 ]
机构
[1] Xenogen Corp, Dept Oncol, Alameda, CA 94501 USA
关键词
imaging; tumour; mouse model; non-invasive;
D O I
10.1002/path.1697
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Significant progress has been made recently in the variety of ways that cancer can be nonimaged invasively in murine tumour models. The development and continued refinement of specialized responsible that enable hardware for an array of small animal imaging methodologies are only partly So too has been the development of new imaging techniques and materials specific, highly sensitive and quantitative measurement of a wide range of tumour-related parameters. Included amongst these new materials are imaging probes that selectively accumulate in tumours, or that become activated by tumour-specific molecules in vivo. Other tumour imaging strategies have been developed that rely upon the detection of reporter transgene expression in vivo, and these too have made a significant impact on both the versatility and the specificity of tumour imaging in living mice. The biological implications resulting from these latest advances are presented here, with particular emphasis on those associated with MRI, PET, SPECT, BLI, and fluorescence-based imaging modalities. Taken together, these advances in tumour imaging are set to have a profound impact on our basic understanding of in vivo tumour biology and will radically alter the application of mouse tumour models in the laboratory. Copyright (C) 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley Sons, Ltd.
引用
收藏
页码:194 / 205
页数:12
相关论文
共 94 条
[11]   MicroPET imaging of breast cancer αv-integrin expression with 64Cu-labeled dimeric RGD peptides [J].
Chen, XY ;
Liu, S ;
Hou, YP ;
Tohme, M ;
Park, R ;
Bading, JR ;
Conti, PS .
MOLECULAR IMAGING AND BIOLOGY, 2004, 6 (05) :350-359
[12]   In vivo tumor imaging using a near-infrared-labeled endostatin molecule [J].
Citrin, D ;
Scott, T ;
Sproull, M ;
Menard, C ;
Tofilon, PJ ;
Camphausen, K .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 58 (02) :536-541
[13]  
Collingridge DR, 2002, CANCER RES, V62, P5912
[14]   Intravital imaging of cell movement in tumours [J].
Condeelis, J ;
Segall, JE .
NATURE REVIEWS CANCER, 2003, 3 (12) :921-930
[15]   It's not just about anatomy: In vivo bioluminescence imaging as an eyepiece into biology [J].
Contag, CH ;
Ross, BD .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2002, 16 (04) :378-387
[16]   Noninvasive imaging of lentiviral-mediated reporter gene expression in living mice [J].
De, A ;
Lewis, XZ ;
Gambhir, SS .
MOLECULAR THERAPY, 2003, 7 (05) :681-691
[17]   Imaging transcriptional regulation of p53-dependent genes with positron emission tomography in vivo [J].
Doubrovin, M ;
Ponomarev, V ;
Beresten, T ;
Balatoni, J ;
Bornmann, W ;
Finn, R ;
Humm, J ;
Larson, S ;
Sadelain, M ;
Blasberg, R ;
Tjuvajev, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9300-9305
[18]   Suppression of anoikis and induction of metastasis by the neurotrophic receptor TrkB [J].
Douma, S ;
van Laar, T ;
Zevenhoven, J ;
Meuwissen, R ;
van Garderen, E ;
Peeper, DS .
NATURE, 2004, 430 (7003) :1034-1040
[19]   Quantitative imaging of the T cell antitumor response by positron-emission tomography [J].
Dubey, P ;
Su, H ;
Adonai, N ;
Du, SY ;
Rosato, A ;
Braun, J ;
Gambhir, SS ;
Witte, ON .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :1232-1237
[20]   Tumor induction of VEGF promoter activity in stromal cells [J].
Fukumura, D ;
Xavier, R ;
Sugiura, T ;
Chen, Y ;
Park, EC ;
Lu, NF ;
Selig, M ;
Nielsen, G ;
Taksir, T ;
Jain, RK ;
Seed, B .
CELL, 1998, 94 (06) :715-725