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The chick chorioallantoic membrane as an in vivo xenograft model for Burkitt lymphoma

BACKGROUND: Burkitt lymphoma (BL) is an aggressive malignancy that arises from B-cells and belongs to the group of Non-Hodgkin lymphomas (NHL). Due to the lack of appropriate in vivo models NHL research is mainly performed in vitro. Here, we studied the use of the chick chorioallantoic membrane (CAM...

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Autores principales: Klingenberg, Marcel, Becker, Jürgen, Eberth, Sonja, Kube, Dieter, Wilting, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036709/
https://www.ncbi.nlm.nih.gov/pubmed/24884418
http://dx.doi.org/10.1186/1471-2407-14-339
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author Klingenberg, Marcel
Becker, Jürgen
Eberth, Sonja
Kube, Dieter
Wilting, Jörg
author_facet Klingenberg, Marcel
Becker, Jürgen
Eberth, Sonja
Kube, Dieter
Wilting, Jörg
author_sort Klingenberg, Marcel
collection PubMed
description BACKGROUND: Burkitt lymphoma (BL) is an aggressive malignancy that arises from B-cells and belongs to the group of Non-Hodgkin lymphomas (NHL). Due to the lack of appropriate in vivo models NHL research is mainly performed in vitro. Here, we studied the use of the chick chorioallantoic membrane (CAM) for the generation of human BL xenograft tumors, which we compared with known characteristics of the human disease. METHODS: In order to generate experimental BL tumors, we inoculated human BL2B95 and BL2-GFP cells on the CAM. BL2B95 xenograft-tumors were grown for seven days and subsequently analyzed with transmission electron and immunofluorescence microscopy, as well as histological staining approaches. BL2-GFP cells were studied at regular intervals up to seven days, and their metastatic behavior was visualized with intravital immunofluorescence techniques. RESULTS: Xenografted BL2B95 cells formed solid tumors in the CAM model with a Ki67-index greater than 90%, preservation of typical tumor markers (CD10, CD19, CD20), a ‘starry sky’ morphology, production of agyrophilic fibers in the stroma, formation of blood and lymphatic vessels and lymphogenic dissemination of BL2B95 to distant sites. We identified macrophages, lymphocytes and heterophilic granulocytes (chick homolog of neutrophils) as the most abundant immune cells in the experimental tumors. BL2-GFP cells could be traced in real-time during their distribution in the CAM, and the first signs for their dissemination were visible after 2-3 days. CONCLUSIONS: We show that xenografted BL2B95 cells generate tumors in the CAM with a high degree of cellular, molecular and proliferative concord with the human disease, supporting the application of the CAM model for NHL research with a focus on tumor-stroma interactions. Additionally we report that BL2-GFP cells, grafted on the CAM of ex ovo cultured chick embryos, provide a powerful tool to study lymphogenic dissemination in real-time.
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spelling pubmed-40367092014-05-29 The chick chorioallantoic membrane as an in vivo xenograft model for Burkitt lymphoma Klingenberg, Marcel Becker, Jürgen Eberth, Sonja Kube, Dieter Wilting, Jörg BMC Cancer Research Article BACKGROUND: Burkitt lymphoma (BL) is an aggressive malignancy that arises from B-cells and belongs to the group of Non-Hodgkin lymphomas (NHL). Due to the lack of appropriate in vivo models NHL research is mainly performed in vitro. Here, we studied the use of the chick chorioallantoic membrane (CAM) for the generation of human BL xenograft tumors, which we compared with known characteristics of the human disease. METHODS: In order to generate experimental BL tumors, we inoculated human BL2B95 and BL2-GFP cells on the CAM. BL2B95 xenograft-tumors were grown for seven days and subsequently analyzed with transmission electron and immunofluorescence microscopy, as well as histological staining approaches. BL2-GFP cells were studied at regular intervals up to seven days, and their metastatic behavior was visualized with intravital immunofluorescence techniques. RESULTS: Xenografted BL2B95 cells formed solid tumors in the CAM model with a Ki67-index greater than 90%, preservation of typical tumor markers (CD10, CD19, CD20), a ‘starry sky’ morphology, production of agyrophilic fibers in the stroma, formation of blood and lymphatic vessels and lymphogenic dissemination of BL2B95 to distant sites. We identified macrophages, lymphocytes and heterophilic granulocytes (chick homolog of neutrophils) as the most abundant immune cells in the experimental tumors. BL2-GFP cells could be traced in real-time during their distribution in the CAM, and the first signs for their dissemination were visible after 2-3 days. CONCLUSIONS: We show that xenografted BL2B95 cells generate tumors in the CAM with a high degree of cellular, molecular and proliferative concord with the human disease, supporting the application of the CAM model for NHL research with a focus on tumor-stroma interactions. Additionally we report that BL2-GFP cells, grafted on the CAM of ex ovo cultured chick embryos, provide a powerful tool to study lymphogenic dissemination in real-time. BioMed Central 2014-05-18 /pmc/articles/PMC4036709/ /pubmed/24884418 http://dx.doi.org/10.1186/1471-2407-14-339 Text en Copyright © 2014 Klingenberg et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Klingenberg, Marcel
Becker, Jürgen
Eberth, Sonja
Kube, Dieter
Wilting, Jörg
The chick chorioallantoic membrane as an in vivo xenograft model for Burkitt lymphoma
title The chick chorioallantoic membrane as an in vivo xenograft model for Burkitt lymphoma
title_full The chick chorioallantoic membrane as an in vivo xenograft model for Burkitt lymphoma
title_fullStr The chick chorioallantoic membrane as an in vivo xenograft model for Burkitt lymphoma
title_full_unstemmed The chick chorioallantoic membrane as an in vivo xenograft model for Burkitt lymphoma
title_short The chick chorioallantoic membrane as an in vivo xenograft model for Burkitt lymphoma
title_sort chick chorioallantoic membrane as an in vivo xenograft model for burkitt lymphoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036709/
https://www.ncbi.nlm.nih.gov/pubmed/24884418
http://dx.doi.org/10.1186/1471-2407-14-339
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