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Imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives
Extrahepatic bile duct cancer (cholangiocarcinoma) has a poor prognosis. Since surgical resection is the only way to prolong the patient’s life, it is of critical importance to correctly determine the extent of lesions. However, conventional pre-operative assessments have insufficient spatial resolu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Japan
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930486/ https://www.ncbi.nlm.nih.gov/pubmed/26842558 http://dx.doi.org/10.1007/s13577-015-0131-5 |
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author | Yokoyama, Hiroshi Sasaki, Ayako Yoshizawa, Tadashi Kijima, Hiroshi Hakamada, Kenichi Yamada, Katsuya |
author_facet | Yokoyama, Hiroshi Sasaki, Ayako Yoshizawa, Tadashi Kijima, Hiroshi Hakamada, Kenichi Yamada, Katsuya |
author_sort | Yokoyama, Hiroshi |
collection | PubMed |
description | Extrahepatic bile duct cancer (cholangiocarcinoma) has a poor prognosis. Since surgical resection is the only way to prolong the patient’s life, it is of critical importance to correctly determine the extent of lesions. However, conventional pre-operative assessments have insufficient spatial resolution for determining the surgical margin. A fluorescent contrast agent might provide a more precise measure to identify anomalies in biliary surface, when combined with probe-based confocal laser endomicroscopy (pCLE). We have previously shown that 2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-l-glucose (2-NBDLG), a fluorescent derivative of l-glucose (fLG), is specifically taken up into spheroids consisting of cells showing heterogeneous nuclear-cytoplasm ratio, a feature of malignant cells in clinical settings. In addition, a combined use of 2-TRLG, a membrane-impermeable fLG, with 2-NBDLG visualized membrane integrity as well. We therefore explored in the present study the availability of the fLGs in vivo as a contrast agent for pCLE by using a hamster model of cholangiocarcinoma. Extrahepatic cholangiocarcinoma developed in mid common duct in ~20 % of the animals subjected to cholecystoduodenostomy with the ligation at the distal end of the common duct followed by injection of a carcinogen N-nitrosobis(2-oxopropyl)amine. After infusing bile duct with a solution containing 2-NBDLG and 2-TRLG, the lumen was surgically exposed and examined by pCLE. Fluorescence pattern characterized by bright spots and dark clumps was detected in the areas diagnosed with cholangiocarcinoma in later histopathology, whereas no such pattern was detected in control animals. These findings may form a basis for elucidating a potential availability of fLGs in imaging cholangiocarcinoma by pCLE. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13577-015-0131-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4930486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-49304862016-07-13 Imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives Yokoyama, Hiroshi Sasaki, Ayako Yoshizawa, Tadashi Kijima, Hiroshi Hakamada, Kenichi Yamada, Katsuya Hum Cell Research Article Extrahepatic bile duct cancer (cholangiocarcinoma) has a poor prognosis. Since surgical resection is the only way to prolong the patient’s life, it is of critical importance to correctly determine the extent of lesions. However, conventional pre-operative assessments have insufficient spatial resolution for determining the surgical margin. A fluorescent contrast agent might provide a more precise measure to identify anomalies in biliary surface, when combined with probe-based confocal laser endomicroscopy (pCLE). We have previously shown that 2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-l-glucose (2-NBDLG), a fluorescent derivative of l-glucose (fLG), is specifically taken up into spheroids consisting of cells showing heterogeneous nuclear-cytoplasm ratio, a feature of malignant cells in clinical settings. In addition, a combined use of 2-TRLG, a membrane-impermeable fLG, with 2-NBDLG visualized membrane integrity as well. We therefore explored in the present study the availability of the fLGs in vivo as a contrast agent for pCLE by using a hamster model of cholangiocarcinoma. Extrahepatic cholangiocarcinoma developed in mid common duct in ~20 % of the animals subjected to cholecystoduodenostomy with the ligation at the distal end of the common duct followed by injection of a carcinogen N-nitrosobis(2-oxopropyl)amine. After infusing bile duct with a solution containing 2-NBDLG and 2-TRLG, the lumen was surgically exposed and examined by pCLE. Fluorescence pattern characterized by bright spots and dark clumps was detected in the areas diagnosed with cholangiocarcinoma in later histopathology, whereas no such pattern was detected in control animals. These findings may form a basis for elucidating a potential availability of fLGs in imaging cholangiocarcinoma by pCLE. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13577-015-0131-5) contains supplementary material, which is available to authorized users. Springer Japan 2016-02-03 2016 /pmc/articles/PMC4930486/ /pubmed/26842558 http://dx.doi.org/10.1007/s13577-015-0131-5 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Article Yokoyama, Hiroshi Sasaki, Ayako Yoshizawa, Tadashi Kijima, Hiroshi Hakamada, Kenichi Yamada, Katsuya Imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives |
title | Imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives |
title_full | Imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives |
title_fullStr | Imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives |
title_full_unstemmed | Imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives |
title_short | Imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives |
title_sort | imaging hamster model of bile duct cancer in vivo using fluorescent l-glucose derivatives |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930486/ https://www.ncbi.nlm.nih.gov/pubmed/26842558 http://dx.doi.org/10.1007/s13577-015-0131-5 |
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