Advancing animal models of neoplasia through in vivo bioluminescence imaging

被引:173
作者
Edinger, M
Cao, YA
Hornig, YS
Jenkins, DE
Verneris, MR
Bachmann, MH
Negrin, RS
Contag, CH [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Radiol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[4] Xenogen Corp, Alameda, CA 94501 USA
关键词
in vivo; bioluminescence; imaging; tumour; animal model;
D O I
10.1016/S0959-8049(02)00410-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant disease is the final manifestation of complex molecular and cellular events leading to uncontrolled cellular proliferation and eventually tissue destruction and metastases. While the in vitro examination of cultured tumour cells permits the molecular dissection of early pathways in tumorigenesis on cellular and subcellular levels, only interrogation of these processes within the complexity of organ systems of the living animal can reveal the full range of pathophysiological changes that occur in neoplastic disease. Such analyses require technologies that facilitate the study of biological processes in vivo, and several approaches have been developed over the last few years. These strategies, in the nascent field of in vivo molecular and cellular imaging, combine molecular biology with imaging modalities as a means to real-time acquisition of functional information about disease processes in living systems. In this review, we will summarise recent developments in in vivo bioluminescence imaging (BLI) and discuss the potential of this imaging strategy for the future of cancer research. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2128 / 2136
页数:9
相关论文
共 36 条
  • [11] Imaging transcriptional regulation of p53-dependent genes with positron emission tomography in vivo
    Doubrovin, M
    Ponomarev, V
    Beresten, T
    Balatoni, J
    Bornmann, W
    Finn, R
    Humm, J
    Larson, S
    Sadelain, M
    Blasberg, R
    Tjuvajev, JG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) : 9300 - 9305
  • [12] Edinger Matthias, 1999, Neoplasia (New York), V1, P303, DOI 10.1038/sj.neo.7900048
  • [13] MEASURING GENE-EXPRESSION WITH LIGHT
    ENGEBRECHT, J
    SIMON, M
    SILVERMAN, M
    [J]. SCIENCE, 1985, 227 (4692) : 1345 - 1347
  • [14] Time-sensitive reversal of hyperplasia in transgenic mice expressing SV40 T antigen
    Ewald, D
    Li, MG
    Efrat, S
    Auer, G
    Wall, RJ
    Furth, PA
    Hennighausen, L
    [J]. SCIENCE, 1996, 273 (5280) : 1384 - 1386
  • [15] Monitoring bioluminescent Staphylococcus aureus infections in living mice using a novel luxABCDE construct
    Francis, KP
    Joh, D
    Bellinger-Kawahara, C
    Hawkinson, MJ
    Purchio, TF
    Contag, PR
    [J]. INFECTION AND IMMUNITY, 2000, 68 (06) : 3594 - 3600
  • [16] Chemistries and colors of bioluminescent reactions: A review
    Hastings, JW
    [J]. GENE, 1996, 173 (01) : 5 - 11
  • [17] Expansion of Philadelphia chromosome-negative CD3+CD56+ cytotoxic cells from chronic myeloid leukemia patients:: In vitro and in vivo efficacy in severe combined immunodeficiency disease mice
    Hoyle, C
    Bangs, CD
    Chang, P
    Kamel, O
    Mehta, B
    Negrin, RS
    [J]. BLOOD, 1998, 92 (09) : 3318 - 3327
  • [18] Doxycycline-mediated quantitative and tissue-specific control of gene expression in transgenic mice
    Kistner, A
    Gossen, M
    Zimmermann, F
    Jerecic, J
    Ullmer, C
    Lubbert, H
    Bujard, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) : 10933 - 10938
  • [19] Novel approaches to monitor bacterial gene expression in infected tissue and host
    Lee, SH
    Camilli, A
    [J]. CURRENT OPINION IN MICROBIOLOGY, 2000, 3 (01) : 97 - 101
  • [20] In utero delivery of adeno-associated viral vectors:: Intraperitoneal gene transfer produces long-term expression
    Lipshutz, GS
    Gruber, CA
    Cao, YA
    Hardy, J
    Contag, CH
    Gaensler, KML
    [J]. MOLECULAR THERAPY, 2001, 3 (03) : 284 - 292