2016
DOI: 10.18632/oncotarget.9066
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Optical imaging probes in oncology

Abstract: Cancer is a complex disease, characterized by alteration of different physiological molecular processes and cellular features. Keeping this in mind, the possibility of early identification and detection of specific tumor biomarkers by non-invasive approaches could improve early diagnosis and patient management.Different molecular imaging procedures provide powerful tools for detection and non-invasive characterization of oncological lesions. Clinical studies are mainly based on the use of computed tomography, … Show more

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Cited by 49 publications
(28 citation statements)
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References 226 publications
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“…Given the relative protein dimensions, the low dye number for optimal streptavidin brightness is consistent with the four to six dyes optimal for antibody brightness ( Vira et al., 2010 ). Brightness is a precious commodity for temporal and spatial resolution in super-resolution microscopy and diagnostic sensitivity ( Liu et al., 2015 , Martelli et al., 2016 ). Notably, dye-NHS labeling of streptavidin led to poor brightness and utility in MHC-tetramer monitoring of immune responses ( Davis et al., 2011 , Ramachandiran et al., 2007 ).…”
Section: Discussionmentioning
confidence: 99%
“…Given the relative protein dimensions, the low dye number for optimal streptavidin brightness is consistent with the four to six dyes optimal for antibody brightness ( Vira et al., 2010 ). Brightness is a precious commodity for temporal and spatial resolution in super-resolution microscopy and diagnostic sensitivity ( Liu et al., 2015 , Martelli et al., 2016 ). Notably, dye-NHS labeling of streptavidin led to poor brightness and utility in MHC-tetramer monitoring of immune responses ( Davis et al., 2011 , Ramachandiran et al., 2007 ).…”
Section: Discussionmentioning
confidence: 99%
“…In this technique, the substrate luciferin is injected into mice in the presence of ATP and oxygen. However, bioluminescence imaging has disadvantages, including instability, fast decay and toxicity (20). Fluorescence imaging uses fluorescent reporter gene labeling and is excited by excitation of fluorescent groups to achieve high energy; this technique emits light in a simple and intuitive manner.…”
Section: Discussionmentioning
confidence: 99%
“…Fluorescence tomography thus results from a complex, multi-step process using light wavelengths in the NIR windows, multiple acquisitions of the fluorescent signal with different geometry, tissue absorption measurement, and complex reconstruction algorithms to determine both absorption and fluorescent maps. Many chemical fluorophores are now available that are compatible with NIR tomographs, enabling a large range of imaging strategies in oncology, including those based on the use of blood pool agents, specific probes, or endogenous enzyme-activable probes [9]. For reporter gene strategies, efforts to discover and to engineer NIR-fluorescent proteins have resulted in reports on several fluorescent proteins to be used for whole-body imaging using NIR tomographs, including IFP1.4 [10] and iRFP [6,7].…”
Section: Discussionmentioning
confidence: 99%