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Non-invasive imaging of engineered human tumors in the living chicken embryo
The growing interest in engineered tumor models prompted us to devise a method for the non-invasive assessment of such models. Here, we report on bioluminescence imaging (BLI) for the assessment of engineered tumor models in the fertilized chicken egg, i.e, chick chorioallantoic membrane (CAM) assay...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504052/ https://www.ncbi.nlm.nih.gov/pubmed/28694510 http://dx.doi.org/10.1038/s41598-017-04572-1 |
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author | Jefferies, Benedict Lenze, Florian Sathe, Anuja Truong, Nguyen Anton, Martina von Eisenhart-Rothe, Rüdiger Nawroth, Roman Mayer-Kuckuk, Philipp |
author_facet | Jefferies, Benedict Lenze, Florian Sathe, Anuja Truong, Nguyen Anton, Martina von Eisenhart-Rothe, Rüdiger Nawroth, Roman Mayer-Kuckuk, Philipp |
author_sort | Jefferies, Benedict |
collection | PubMed |
description | The growing interest in engineered tumor models prompted us to devise a method for the non-invasive assessment of such models. Here, we report on bioluminescence imaging (BLI) for the assessment of engineered tumor models in the fertilized chicken egg, i.e, chick chorioallantoic membrane (CAM) assay. One prostate cancer (PC-3) and two osteosarcoma (MG63 and HOS) cell lines were modified with luciferase reporter genes. To create engineered tumors, these cell lines were seeded either onto basement membrane extract (BME) or gelfoam scaffolds, and subsequently grafted in vivo onto the CAM. BLI enabled non-invasive, specific detection of the engineered tumors on the CAM in the living chicken embryo. Further, BLI permitted daily, quantitative monitoring of the engineered tumors over the course of up to 7 days. Data showed that an extracellular matrix (ECM) composed of BME supported growth of reporter gene marked PC-3 tumors but did not support MG63 or HOS tumor growth. However, MG63 tumors engineered on the collagen-based gelfoam ECM showed a temporal proliferation burst in MG63 tumors. Together, the data demonstrated imaging of engineered human cancer models in living chicken embryos. The combination of CAM assay and BLI holds significant potential for the examination of a broad range of engineered tumor models. |
format | Online Article Text |
id | pubmed-5504052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55040522017-07-12 Non-invasive imaging of engineered human tumors in the living chicken embryo Jefferies, Benedict Lenze, Florian Sathe, Anuja Truong, Nguyen Anton, Martina von Eisenhart-Rothe, Rüdiger Nawroth, Roman Mayer-Kuckuk, Philipp Sci Rep Article The growing interest in engineered tumor models prompted us to devise a method for the non-invasive assessment of such models. Here, we report on bioluminescence imaging (BLI) for the assessment of engineered tumor models in the fertilized chicken egg, i.e, chick chorioallantoic membrane (CAM) assay. One prostate cancer (PC-3) and two osteosarcoma (MG63 and HOS) cell lines were modified with luciferase reporter genes. To create engineered tumors, these cell lines were seeded either onto basement membrane extract (BME) or gelfoam scaffolds, and subsequently grafted in vivo onto the CAM. BLI enabled non-invasive, specific detection of the engineered tumors on the CAM in the living chicken embryo. Further, BLI permitted daily, quantitative monitoring of the engineered tumors over the course of up to 7 days. Data showed that an extracellular matrix (ECM) composed of BME supported growth of reporter gene marked PC-3 tumors but did not support MG63 or HOS tumor growth. However, MG63 tumors engineered on the collagen-based gelfoam ECM showed a temporal proliferation burst in MG63 tumors. Together, the data demonstrated imaging of engineered human cancer models in living chicken embryos. The combination of CAM assay and BLI holds significant potential for the examination of a broad range of engineered tumor models. Nature Publishing Group UK 2017-07-10 /pmc/articles/PMC5504052/ /pubmed/28694510 http://dx.doi.org/10.1038/s41598-017-04572-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jefferies, Benedict Lenze, Florian Sathe, Anuja Truong, Nguyen Anton, Martina von Eisenhart-Rothe, Rüdiger Nawroth, Roman Mayer-Kuckuk, Philipp Non-invasive imaging of engineered human tumors in the living chicken embryo |
title | Non-invasive imaging of engineered human tumors in the living chicken embryo |
title_full | Non-invasive imaging of engineered human tumors in the living chicken embryo |
title_fullStr | Non-invasive imaging of engineered human tumors in the living chicken embryo |
title_full_unstemmed | Non-invasive imaging of engineered human tumors in the living chicken embryo |
title_short | Non-invasive imaging of engineered human tumors in the living chicken embryo |
title_sort | non-invasive imaging of engineered human tumors in the living chicken embryo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504052/ https://www.ncbi.nlm.nih.gov/pubmed/28694510 http://dx.doi.org/10.1038/s41598-017-04572-1 |
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