In vivo molecular imaging of colorectal cancer using quantum dots targeted to vascular endothelial growth factor receptor 2 and optical coherence tomography/laser-induced fluorescence dual-modality imaging

被引:24
作者
Carbary-Ganz, Jordan L. [1 ]
Welge, Weston A. [1 ]
Barton, Jennifer K. [1 ]
Utzinger, Urs [1 ]
机构
[1] Univ Arizona, Biomed Engn, Tucson, AZ 84721 USA
基金
美国国家卫生研究院;
关键词
quantum dots; molecular imaging; colorectal cancer; in vivo; optical coherence tomography; fluorescence spectroscopy; dual-modality; microendoscope; TUMOR MICROENVIRONMENT; PANCREATIC-CANCER; XENOGRAFT MODELS; MOUSE MODEL; COLON; EXPRESSION; ANTIBODY; BEVACIZUMAB; METASTASIS; THERAPY;
D O I
10.1117/1.JBO.20.9.096015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Optical coherence tomography/laser induced fluorescence (OCT/LIF) dual-modality imaging allows for minimally invasive, nondestructive endoscopic visualization of colorectal cancer in mice. This technology enables simultaneous longitudinal tracking of morphological (OCT) and biochemical (fluorescence) changes as colorectal cancer develops, compared to current methods of colorectal cancer screening in humans that rely on morphological changes alone. We have shown that QDot655 targeted to vascular endothelial growth factor receptor 2 (QD655-VEGFR2) can be applied to the colon of carcinogen-treated mice and provides significantly increased contrast between the diseased and undiseased tissue with high sensitivity and specificity ex vivo. QD655-VEGFR2 was used in a longitudinal in vivo study to investigate the ability to correlate fluorescence signal to tumor development. QD655-VEGFR2 was applied to the colon of azoxymethane (AOM-) or saline-treated control mice in vivo via lavage. OCT/LIF images of the distal colon were taken at five consecutive time points every three weeks after the final AOM injection. Difficulties in fully flushing unbound contrast agent from the colon led to variable background signal; however, a spatial correlation was found between tumors identified in OCT images, and high fluorescence intensity of the QD655 signal, demonstrating the ability to detect VEGFR2 expressing tumors in vivo. (C) 2015 Society of Photo-Optical Instrumentation Engineers (SPIE)
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页数:9
相关论文
共 59 条
[1]   Nanocrystal targeting in vivo [J].
Åkerman, ME ;
Chan, WCW ;
Laakkonen, P ;
Bhatia, SN ;
Ruoslahti, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12617-12621
[2]  
[Anonymous], 2015, CANC FACTS FIG 2015
[3]   Sentinel lymph node imaging using quantum dots in mouse tumor models [J].
Ballou, Byron ;
Ernst, Lauren A. ;
Andreko, Susan ;
Harper, Theresa ;
Fitzpatrick, James A. J. ;
Waggoner, Alan S. ;
Bruchez, Marcel P. .
BIOCONJUGATE CHEMISTRY, 2007, 18 (02) :389-396
[4]   Evaluation of hypericin-mediated photodynamic therapy in combination with angiogenesis inhibitor bevacizumab using in vivo fluorescence confocal endomicroscopy [J].
Bhuvaneswari, Ramaswamy ;
Thong, Patricia S. P. ;
Gan, Yik-Yuen ;
Soo, Khee-Chee ;
Olivo, Malini .
JOURNAL OF BIOMEDICAL OPTICS, 2010, 15 (01)
[5]   Bioconjugated quantum dots for cancer research: Present status, prospects and remaining issues (vol 28, pg 199, 2010) [J].
Biju, Vasudevanpillai ;
Mundayoor, Sathish ;
Omkumar, Ramakrishnapillai V. ;
Anas, Abdulaziz ;
Ishikawa, Mitsuru .
BIOTECHNOLOGY ADVANCES, 2011, 29 (02) :259-260
[6]   Peptide-labeled near-infrared quantum dots for imaging tumor vasculature in living subjects [J].
Cai, WB ;
Shin, DW ;
Chen, K ;
Gheysens, O ;
Cao, QZ ;
Wang, SX ;
Gambhir, SS ;
Chen, XY .
NANO LETTERS, 2006, 6 (04) :669-676
[7]   Quantum dots targeted to vascular endothelial growth factor receptor 2 as a contrast agent for the detection of colorectal cancer [J].
Carbary-Ganz, Jordan L. ;
Barton, Jennifer K. ;
Utzinger, Urs .
JOURNAL OF BIOMEDICAL OPTICS, 2014, 19 (08)
[8]   Design of new quantum dot materials for deep tissue infrared imaging [J].
Cassette, Elsa ;
Helle, Marion ;
Bezdetnaya, Lina ;
Marchal, Frederic ;
Dubertret, Benoit ;
Pons, Thomas .
ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (05) :719-731
[9]   In vivo cancer imaging by poly(ethylene glycol)-b-poly(ε-caprolactone) micelles containing a near-infrared probe [J].
Cho, Hyunah ;
Indig, Guilherme L. ;
Weichert, Jamey ;
Shin, Ho-Chul ;
Kwon, Glen S. .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2012, 8 (02) :228-236
[10]   VEGF-targeted therapy: mechanisms of anti-tumour activity [J].
Ellis, Lee M. ;
Hicklin, Daniel J. .
NATURE REVIEWS CANCER, 2008, 8 (08) :579-591