High-Resolution Optical Molecular Imaging of Changes in Choline Metabolism in Oral Neoplasia
This study was aimed at developing an optical molecular imaging approach to measure differences in uptake and intracellular retention of choline in clinically isolated tissue biopsies from head and neck cancer patients. An optically detectable analogue of choline (propargyl choline) was synthesized...
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2013-02-01
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Series: | Translational Oncology |
Online Access: | http://www.sciencedirect.com/science/article/pii/S193652331380040X |
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doaj-c3c9a7d3bcc545e6a86304226a933aa12020-11-24T22:00:29ZengElsevierTranslational Oncology1936-52332013-02-01613341High-Resolution Optical Molecular Imaging of Changes in Choline Metabolism in Oral NeoplasiaZhen Luo0Melissa Loja1D. Greg Farwell2Quang C. Luu3Paul J. Donald4Deborah Amott5Regina Gandour-Edwards6Nitin Nitin7Department of Biological and Agricultural Engineering, University of California, Davis, Davis, CASchool of Medicine, University of California, Davis, Davis, CADepartment of Otolaryngology, University of California, Davis, Davis, CADepartment of Otolaryngology, University of California, Davis, Davis, CADepartment of Otolaryngology, University of California, Davis, Davis, CADepartment of Otolaryngology, University of California, Davis, Davis, CADepartment of Pathology and Laboratory Medicine, University of California, Davis, Davis, CADepartment of Biological and Agricultural Engineering, University of California, Davis, Davis, CA; Food Science and Technology, University of California, Davis, Davis, CA; Address all correspondence to: Nitin Nitin, PhD, Department of Biological Engineering, University of California, Davis, One Shields Avenue, Davis, CA 95616.This study was aimed at developing an optical molecular imaging approach to measure differences in uptake and intracellular retention of choline in clinically isolated tissue biopsies from head and neck cancer patients. An optically detectable analogue of choline (propargyl choline) was synthesized and evaluated in 2D and 3D models and clinically isolated paired biopsies (n = 22 biopsies). Fluorescence contrast between clinically abnormal and normal tissues based on uptake and intracellular retention of propargyl choline was measured and correlated with pathologic diagnosis. Results in 2D and 3D models demonstrated a rapid uptake of propargyl choline in cancer cells, uniform permeation in tissue models, and specific detection of intracellular entrapped propargyl choline using the click chemistry reaction with an azide-modified Alexa 488 dye. Fluorescence imaging measurements following topical delivery of propargyl choline in clinically isolated biopsies showed that the mean fluorescence intensity (MFI) of neoplastic tissues was four-fold to five-fold higher than the MFI of clinically and pathologically normal samples. This difference in fluorescence contrast was measured on the basis of comparison of paired biopsy sets isolated from individual patients as well as comparison of clinically abnormal and normal biopsies independent of anatomic locations in the head and neck cavity and across diverse patients. In conclusion, a novel imaging approach based on monoalkyne-modified choline was developed and validated using cell and tissue models. Results in clinically isolated tissue biopsies demonstrate a significant fluorescent contrast between neoplastic and normal tissues and illustrate high specificity of the optical imaging approach.http://www.sciencedirect.com/science/article/pii/S193652331380040X |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zhen Luo Melissa Loja D. Greg Farwell Quang C. Luu Paul J. Donald Deborah Amott Regina Gandour-Edwards Nitin Nitin |
spellingShingle |
Zhen Luo Melissa Loja D. Greg Farwell Quang C. Luu Paul J. Donald Deborah Amott Regina Gandour-Edwards Nitin Nitin High-Resolution Optical Molecular Imaging of Changes in Choline Metabolism in Oral Neoplasia Translational Oncology |
author_facet |
Zhen Luo Melissa Loja D. Greg Farwell Quang C. Luu Paul J. Donald Deborah Amott Regina Gandour-Edwards Nitin Nitin |
author_sort |
Zhen Luo |
title |
High-Resolution Optical Molecular Imaging of Changes in Choline Metabolism in Oral Neoplasia |
title_short |
High-Resolution Optical Molecular Imaging of Changes in Choline Metabolism in Oral Neoplasia |
title_full |
High-Resolution Optical Molecular Imaging of Changes in Choline Metabolism in Oral Neoplasia |
title_fullStr |
High-Resolution Optical Molecular Imaging of Changes in Choline Metabolism in Oral Neoplasia |
title_full_unstemmed |
High-Resolution Optical Molecular Imaging of Changes in Choline Metabolism in Oral Neoplasia |
title_sort |
high-resolution optical molecular imaging of changes in choline metabolism in oral neoplasia |
publisher |
Elsevier |
series |
Translational Oncology |
issn |
1936-5233 |
publishDate |
2013-02-01 |
description |
This study was aimed at developing an optical molecular imaging approach to measure differences in uptake and intracellular retention of choline in clinically isolated tissue biopsies from head and neck cancer patients. An optically detectable analogue of choline (propargyl choline) was synthesized and evaluated in 2D and 3D models and clinically isolated paired biopsies (n = 22 biopsies). Fluorescence contrast between clinically abnormal and normal tissues based on uptake and intracellular retention of propargyl choline was measured and correlated with pathologic diagnosis. Results in 2D and 3D models demonstrated a rapid uptake of propargyl choline in cancer cells, uniform permeation in tissue models, and specific detection of intracellular entrapped propargyl choline using the click chemistry reaction with an azide-modified Alexa 488 dye. Fluorescence imaging measurements following topical delivery of propargyl choline in clinically isolated biopsies showed that the mean fluorescence intensity (MFI) of neoplastic tissues was four-fold to five-fold higher than the MFI of clinically and pathologically normal samples. This difference in fluorescence contrast was measured on the basis of comparison of paired biopsy sets isolated from individual patients as well as comparison of clinically abnormal and normal biopsies independent of anatomic locations in the head and neck cavity and across diverse patients. In conclusion, a novel imaging approach based on monoalkyne-modified choline was developed and validated using cell and tissue models. Results in clinically isolated tissue biopsies demonstrate a significant fluorescent contrast between neoplastic and normal tissues and illustrate high specificity of the optical imaging approach. |
url |
http://www.sciencedirect.com/science/article/pii/S193652331380040X |
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