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Precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus

BACKGROUND: Current methods of image-guided surgery of tumours of the lung mostly rely on CT. A sensitive procedure of selective tumour fluorescence labelling would allow simple and high-resolution visualisation of the tumour for precise surgical navigation. METHODS: Human lung cancer cell lines H46...

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Autores principales: Yano, Shuya, Zhang, Yong, Miwa, Shinji, Kishimoto, Hiroyuki, Urata, Yasuo, Bouvet, Michael, Kagawa, Shunsuke, Fujiwara, Toshiyoshi, Hoffman, Robert M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567685/
https://www.ncbi.nlm.nih.gov/pubmed/26380093
http://dx.doi.org/10.1136/bmjresp-2015-000096
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author Yano, Shuya
Zhang, Yong
Miwa, Shinji
Kishimoto, Hiroyuki
Urata, Yasuo
Bouvet, Michael
Kagawa, Shunsuke
Fujiwara, Toshiyoshi
Hoffman, Robert M
author_facet Yano, Shuya
Zhang, Yong
Miwa, Shinji
Kishimoto, Hiroyuki
Urata, Yasuo
Bouvet, Michael
Kagawa, Shunsuke
Fujiwara, Toshiyoshi
Hoffman, Robert M
author_sort Yano, Shuya
collection PubMed
description BACKGROUND: Current methods of image-guided surgery of tumours of the lung mostly rely on CT. A sensitive procedure of selective tumour fluorescence labelling would allow simple and high-resolution visualisation of the tumour for precise surgical navigation. METHODS: Human lung cancer cell lines H460 and A549 were genetically transformed to express red fluorescent protein (RFP). Tumours were grown subcutaneously for each cell line and harvested and minced for surgical orthotopic implantation on the left lung of nude mice. Tumour growth was measured by fluorescence imaging. After the tumours reached 5 mm in diameter, they were injected under fluorescence guidance with the telomerase-dependent green fluorescent protein (GFP)-containing adenovirus, OBP-401. Viral labelling of the lung tumours with GFP precisely colocalised with tumour RFP expression. Three days after administration of OBP-401, fluorescence-guided surgery (FGS) was performed. RESULTS: FGS of tumours in the lung was enabled by labelling with a telomerase-dependent adenovirus containing the GFP gene. Tumours in the lung were selectively and brightly labelled. FGS enabled complete lung tumour resection with no residual fluorescent tumour. CONCLUSIONS: FGS of tumours in the lung is feasible and more effective than bright-light surgery.
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spelling pubmed-45676852015-09-14 Precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus Yano, Shuya Zhang, Yong Miwa, Shinji Kishimoto, Hiroyuki Urata, Yasuo Bouvet, Michael Kagawa, Shunsuke Fujiwara, Toshiyoshi Hoffman, Robert M BMJ Open Respir Res Lung Cancer BACKGROUND: Current methods of image-guided surgery of tumours of the lung mostly rely on CT. A sensitive procedure of selective tumour fluorescence labelling would allow simple and high-resolution visualisation of the tumour for precise surgical navigation. METHODS: Human lung cancer cell lines H460 and A549 were genetically transformed to express red fluorescent protein (RFP). Tumours were grown subcutaneously for each cell line and harvested and minced for surgical orthotopic implantation on the left lung of nude mice. Tumour growth was measured by fluorescence imaging. After the tumours reached 5 mm in diameter, they were injected under fluorescence guidance with the telomerase-dependent green fluorescent protein (GFP)-containing adenovirus, OBP-401. Viral labelling of the lung tumours with GFP precisely colocalised with tumour RFP expression. Three days after administration of OBP-401, fluorescence-guided surgery (FGS) was performed. RESULTS: FGS of tumours in the lung was enabled by labelling with a telomerase-dependent adenovirus containing the GFP gene. Tumours in the lung were selectively and brightly labelled. FGS enabled complete lung tumour resection with no residual fluorescent tumour. CONCLUSIONS: FGS of tumours in the lung is feasible and more effective than bright-light surgery. BMJ Publishing Group 2015-09-07 /pmc/articles/PMC4567685/ /pubmed/26380093 http://dx.doi.org/10.1136/bmjresp-2015-000096 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Lung Cancer
Yano, Shuya
Zhang, Yong
Miwa, Shinji
Kishimoto, Hiroyuki
Urata, Yasuo
Bouvet, Michael
Kagawa, Shunsuke
Fujiwara, Toshiyoshi
Hoffman, Robert M
Precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus
title Precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus
title_full Precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus
title_fullStr Precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus
title_full_unstemmed Precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus
title_short Precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus
title_sort precise navigation surgery of tumours in the lung in mouse models enabled by in situ fluorescence labelling with a killer-reporter adenovirus
topic Lung Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567685/
https://www.ncbi.nlm.nih.gov/pubmed/26380093
http://dx.doi.org/10.1136/bmjresp-2015-000096
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