DocumentCode :
755186
Title :
Using in Vivo Bioluminescence Imaging to Shed Light on Cancer Biology
Author :
Thorne, Steve H. ; Contag, Christopher H.
Author_Institution :
Molecular Imaging Program, Stanford Sch. of Med., CA, USA
Volume :
93
Issue :
4
fYear :
2005
fDate :
4/1/2005 12:00:00 AM
Firstpage :
750
Lastpage :
762
Abstract :
Luciferases are light-emitting enzymes that have been used as reporters of biological function for several decades, and have more recently been used as reporters for the study of biological processes in living animals. Although these enzymes appear to have evolved independently in different species, they are all oxygenases that require energy, a chemical substrate, and oxygen. The technologies of detecting their weak bioluminescent signals in the bodies of living rodent models of human biology and disease, comprise the optical imaging method called in vivo bioluminescence imaging (BLI). BLI has been applied to a number of questions in cancer research, including studies of tumor burden, response to therapy, assessment of gene expression, and development of metastatic lesions. The considerations necessary for evaluating image data obtained by this method, the advances in technology development, and recent applications in the study of cancer are the focus of this paper.
Keywords :
bioluminescence; biomedical imaging; cancer; biological function; biological processes; bioluminescence imaging; bioluminescent signals; cancer biology; cancer research; chemical substrate; functional imaging; human biology; light emitting enzymes; living rodent models; luciferases; metastatic lesions; molecular imaging; optical imaging; oxygenases; Animals; Biochemistry; Biological processes; Biological system modeling; Bioluminescence; Cancer; Chemical technology; In vivo; Optical imaging; Rodents; Functional imaging; molecular imaging; multimodality;
fLanguage :
English
Journal_Title :
Proceedings of the IEEE
Publisher :
ieee
ISSN :
0018-9219
Type :
jour
DOI :
10.1109/JPROC.2005.844261
Filename :
1412102
Link To Document :
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