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The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice

BACKGROUND: The preclinical development of anti-sarcoma drugs has been primarily based on the subcutaneous transplantation of xenografts. Transplant survival remains an obstacle of current models which has been attributed to the period of hypoxia after transplantation. We hypothesized that primary s...

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Autores principales: Tilkorn, Daniel Johannes, Al-Benna, Sammy, Hauser, Joerg, Ring, Andrej, Steinstraesser, Lars, Daigeler, Adrien, Schmitz, Inge, Steinau, Hans Ulrich, Stricker, Ingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649888/
https://www.ncbi.nlm.nih.gov/pubmed/29147279
http://dx.doi.org/10.4021/wjon496w
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author Tilkorn, Daniel Johannes
Al-Benna, Sammy
Hauser, Joerg
Ring, Andrej
Steinstraesser, Lars
Daigeler, Adrien
Schmitz, Inge
Steinau, Hans Ulrich
Stricker, Ingo
author_facet Tilkorn, Daniel Johannes
Al-Benna, Sammy
Hauser, Joerg
Ring, Andrej
Steinstraesser, Lars
Daigeler, Adrien
Schmitz, Inge
Steinau, Hans Ulrich
Stricker, Ingo
author_sort Tilkorn, Daniel Johannes
collection PubMed
description BACKGROUND: The preclinical development of anti-sarcoma drugs has been primarily based on the subcutaneous transplantation of xenografts. Transplant survival remains an obstacle of current models which has been attributed to the period of hypoxia after transplantation. We hypothesized that primary soft tissue sarcoma models with an intrinsic tissue engineered vascular supply would be easily reproducible. The aim of this study was to establish a model of primary human soft tissue sarcoma with an intrinsic vascular supply. METHODS: Primary soft tissue sarcoma cells from resected human liposarcomas isolated and divided into tumour fragments were transplanted into a silicon chamber, placed around the superficial epigastric vessels in mice. Sarcoma xenograft samples were analysed histomorphologically (light/electron microscopy and immunohistochemistry). RESULTS: All primary soft tissue sarcoma transplants engrafted, leading to solid tumours within 3 weeks. Histological and immunohistochemical staining confirmed the mouse xenografts as identical high grade liposarcomas compared to original tumour tissue. CONCLUSION: This study established a reproducible xenograft model of primary human liposarcoma. This animal model could be of high value for studying human soft tissue sarcomas and their therapy.
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spelling pubmed-56498882017-11-16 The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice Tilkorn, Daniel Johannes Al-Benna, Sammy Hauser, Joerg Ring, Andrej Steinstraesser, Lars Daigeler, Adrien Schmitz, Inge Steinau, Hans Ulrich Stricker, Ingo World J Oncol Original Article BACKGROUND: The preclinical development of anti-sarcoma drugs has been primarily based on the subcutaneous transplantation of xenografts. Transplant survival remains an obstacle of current models which has been attributed to the period of hypoxia after transplantation. We hypothesized that primary soft tissue sarcoma models with an intrinsic tissue engineered vascular supply would be easily reproducible. The aim of this study was to establish a model of primary human soft tissue sarcoma with an intrinsic vascular supply. METHODS: Primary soft tissue sarcoma cells from resected human liposarcomas isolated and divided into tumour fragments were transplanted into a silicon chamber, placed around the superficial epigastric vessels in mice. Sarcoma xenograft samples were analysed histomorphologically (light/electron microscopy and immunohistochemistry). RESULTS: All primary soft tissue sarcoma transplants engrafted, leading to solid tumours within 3 weeks. Histological and immunohistochemical staining confirmed the mouse xenografts as identical high grade liposarcomas compared to original tumour tissue. CONCLUSION: This study established a reproducible xenograft model of primary human liposarcoma. This animal model could be of high value for studying human soft tissue sarcomas and their therapy. Elmer Press 2012-04 2012-04-23 /pmc/articles/PMC5649888/ /pubmed/29147279 http://dx.doi.org/10.4021/wjon496w Text en Copyright 2012, Tilkorn et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tilkorn, Daniel Johannes
Al-Benna, Sammy
Hauser, Joerg
Ring, Andrej
Steinstraesser, Lars
Daigeler, Adrien
Schmitz, Inge
Steinau, Hans Ulrich
Stricker, Ingo
The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice
title The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice
title_full The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice
title_fullStr The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice
title_full_unstemmed The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice
title_short The Vascularised Groin Chamber: A Novel Model for Growing Primary Human Liposarcoma in Nude Mice
title_sort vascularised groin chamber: a novel model for growing primary human liposarcoma in nude mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649888/
https://www.ncbi.nlm.nih.gov/pubmed/29147279
http://dx.doi.org/10.4021/wjon496w
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