Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Yokoyama, Hiroshi, Sasaki, Ayako, Yoshizawa, Tadashi, Kijima, Hiroshi, Hakamada, Kenichi, Yamada, Katsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2016
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
_version_ 1782440749406617600
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
work_keys_str_mv AT yokoyamahiroshi imaginghamstermodelofbileductcancerinvivousingfluorescentlglucosederivatives
AT sasakiayako imaginghamstermodelofbileductcancerinvivousingfluorescentlglucosederivatives
AT yoshizawatadashi imaginghamstermodelofbileductcancerinvivousingfluorescentlglucosederivatives
AT kijimahiroshi imaginghamstermodelofbileductcancerinvivousingfluorescentlglucosederivatives
AT hakamadakenichi imaginghamstermodelofbileductcancerinvivousingfluorescentlglucosederivatives
AT yamadakatsuya imaginghamstermodelofbileductcancerinvivousingfluorescentlglucosederivatives