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Morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane

BACKGROUND: The chick chorio-allantoic membrane (CAM) assay is a commonly used method for studying angiogenic or anti-angiogenic activities in vivo. The ease of access allows direct monitoring of tumour growth by biomicroscopy and the possibility to screen many samples in an inexpensive way. The CAM...

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Autores principales: Balke, Maurice, Neumann, Anna, Kersting, Christian, Agelopoulos, Konstantin, Gebert, Carsten, Gosheger, Georg, Buerger, Horst, Hagedorn, Martin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838906/
https://www.ncbi.nlm.nih.gov/pubmed/20202196
http://dx.doi.org/10.1186/1756-0500-3-58
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author Balke, Maurice
Neumann, Anna
Kersting, Christian
Agelopoulos, Konstantin
Gebert, Carsten
Gosheger, Georg
Buerger, Horst
Hagedorn, Martin
author_facet Balke, Maurice
Neumann, Anna
Kersting, Christian
Agelopoulos, Konstantin
Gebert, Carsten
Gosheger, Georg
Buerger, Horst
Hagedorn, Martin
author_sort Balke, Maurice
collection PubMed
description BACKGROUND: The chick chorio-allantoic membrane (CAM) assay is a commonly used method for studying angiogenic or anti-angiogenic activities in vivo. The ease of access allows direct monitoring of tumour growth by biomicroscopy and the possibility to screen many samples in an inexpensive way. The CAM model provides a powerful tool to study effects of molecules, which interfere with physiological angiogenesis, or experimental tumours derived from cancer cell lines. We therefore screened eight osteosarcoma cell lines for their ability to form vascularized tumours on the CAM. FINDINGS: We implanted 3-5 million cells of human osteosarcoma lines (HOS, MG63, MNNG-HOS, OST, SAOS, SJSA1, U2OS, ZK58) on the CAM at day 10 of embryonic development. Tumour growth was monitored by in vivo biomicroscopy at different time points and tumours were fixed in paraformaldehyde seven days after cell grafting. The tissue was observed, photographed and selected cases were further analyzed using standard histology. From the eight cell lines the MNNG-HOS, U2OS and SAOS were able to form solid tumours when grafted on the CAM. The MNNG-HOS tumours showed the most reliable and consistent growth and were able to penetrate the chorionic epithelium, grow in the CAM stroma and induce a strong angiogenic response. CONCLUSIONS: Our results show that the CAM assay is a useful tool for studying osteosarcoma growth. The model provides an excellent alternative to current rodent models and could serve as a preclinical screening assay for anticancer molecules. It might increase the speed and efficacy of the development of new drugs for the treatment of osteosarcoma.
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spelling pubmed-28389062010-03-16 Morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane Balke, Maurice Neumann, Anna Kersting, Christian Agelopoulos, Konstantin Gebert, Carsten Gosheger, Georg Buerger, Horst Hagedorn, Martin BMC Res Notes Short Report BACKGROUND: The chick chorio-allantoic membrane (CAM) assay is a commonly used method for studying angiogenic or anti-angiogenic activities in vivo. The ease of access allows direct monitoring of tumour growth by biomicroscopy and the possibility to screen many samples in an inexpensive way. The CAM model provides a powerful tool to study effects of molecules, which interfere with physiological angiogenesis, or experimental tumours derived from cancer cell lines. We therefore screened eight osteosarcoma cell lines for their ability to form vascularized tumours on the CAM. FINDINGS: We implanted 3-5 million cells of human osteosarcoma lines (HOS, MG63, MNNG-HOS, OST, SAOS, SJSA1, U2OS, ZK58) on the CAM at day 10 of embryonic development. Tumour growth was monitored by in vivo biomicroscopy at different time points and tumours were fixed in paraformaldehyde seven days after cell grafting. The tissue was observed, photographed and selected cases were further analyzed using standard histology. From the eight cell lines the MNNG-HOS, U2OS and SAOS were able to form solid tumours when grafted on the CAM. The MNNG-HOS tumours showed the most reliable and consistent growth and were able to penetrate the chorionic epithelium, grow in the CAM stroma and induce a strong angiogenic response. CONCLUSIONS: Our results show that the CAM assay is a useful tool for studying osteosarcoma growth. The model provides an excellent alternative to current rodent models and could serve as a preclinical screening assay for anticancer molecules. It might increase the speed and efficacy of the development of new drugs for the treatment of osteosarcoma. BioMed Central 2010-03-04 /pmc/articles/PMC2838906/ /pubmed/20202196 http://dx.doi.org/10.1186/1756-0500-3-58 Text en Copyright ©2010 Balke 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 cited.
spellingShingle Short Report
Balke, Maurice
Neumann, Anna
Kersting, Christian
Agelopoulos, Konstantin
Gebert, Carsten
Gosheger, Georg
Buerger, Horst
Hagedorn, Martin
Morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane
title Morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane
title_full Morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane
title_fullStr Morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane
title_full_unstemmed Morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane
title_short Morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane
title_sort morphologic characterization of osteosarcoma growth on the chick chorioallantoic membrane
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838906/
https://www.ncbi.nlm.nih.gov/pubmed/20202196
http://dx.doi.org/10.1186/1756-0500-3-58
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