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Tissue Engineering of a Human 3D in vitro Tumor Test System

Cancer is one of the leading causes of death worldwide. Current therapeutic strategies are predominantly developed in 2D culture systems, which inadequately reflect physiological conditions in vivo. Biological 3D matrices provide cells an environment in which cells can self-organize, allowing the st...

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Autores principales: Moll, Corinna, Reboredo, Jenny, Schwarz, Thomas, Appelt, Antje, Schürlein, Sebastian, Walles, Heike, Nietzer, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846813/
https://www.ncbi.nlm.nih.gov/pubmed/23963401
http://dx.doi.org/10.3791/50460
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author Moll, Corinna
Reboredo, Jenny
Schwarz, Thomas
Appelt, Antje
Schürlein, Sebastian
Walles, Heike
Nietzer, Sarah
author_facet Moll, Corinna
Reboredo, Jenny
Schwarz, Thomas
Appelt, Antje
Schürlein, Sebastian
Walles, Heike
Nietzer, Sarah
author_sort Moll, Corinna
collection PubMed
description Cancer is one of the leading causes of death worldwide. Current therapeutic strategies are predominantly developed in 2D culture systems, which inadequately reflect physiological conditions in vivo. Biological 3D matrices provide cells an environment in which cells can self-organize, allowing the study of tissue organization and cell differentiation. Such scaffolds can be seeded with a mixture of different cell types to study direct 3D cell-cell-interactions. To mimic the 3D complexity of cancer tumors, our group has developed a 3D in vitro tumor test system. Our 3D tissue test system models the in vivo situation of malignant peripheral nerve sheath tumors (MPNSTs), which we established with our decellularized porcine jejunal segment derived biological vascularized scaffold (BioVaSc). In our model, we reseeded a modified BioVaSc matrix with primary fibroblasts, microvascular endothelial cells (mvECs) and the S462 tumor cell line. For static culture, the vascular structure of the BioVaSc is removed and the remaining scaffold is cut open on one side (Small Intestinal Submucosa SIS-Muc). The resulting matrix is then fixed between two metal rings (cell crowns). Another option is to culture the cell-seeded SIS-Muc in a flow bioreactor system that exposes the cells to shear stress. Here, the bioreactor is connected to a peristaltic pump in a self-constructed incubator. A computer regulates the arterial oxygen and nutrient supply via parameters such as blood pressure, temperature, and flow rate. This setup allows for a dynamic culture with either pressure-regulated pulsatile or constant flow. In this study, we could successfully establish both a static and dynamic 3D culture system for MPNSTs. The ability to model cancer tumors in a more natural 3D environment will enable the discovery, testing, and validation of future pharmaceuticals in a human-like model.
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spelling pubmed-38468132013-12-17 Tissue Engineering of a Human 3D in vitro Tumor Test System Moll, Corinna Reboredo, Jenny Schwarz, Thomas Appelt, Antje Schürlein, Sebastian Walles, Heike Nietzer, Sarah J Vis Exp Cancer Biology Cancer is one of the leading causes of death worldwide. Current therapeutic strategies are predominantly developed in 2D culture systems, which inadequately reflect physiological conditions in vivo. Biological 3D matrices provide cells an environment in which cells can self-organize, allowing the study of tissue organization and cell differentiation. Such scaffolds can be seeded with a mixture of different cell types to study direct 3D cell-cell-interactions. To mimic the 3D complexity of cancer tumors, our group has developed a 3D in vitro tumor test system. Our 3D tissue test system models the in vivo situation of malignant peripheral nerve sheath tumors (MPNSTs), which we established with our decellularized porcine jejunal segment derived biological vascularized scaffold (BioVaSc). In our model, we reseeded a modified BioVaSc matrix with primary fibroblasts, microvascular endothelial cells (mvECs) and the S462 tumor cell line. For static culture, the vascular structure of the BioVaSc is removed and the remaining scaffold is cut open on one side (Small Intestinal Submucosa SIS-Muc). The resulting matrix is then fixed between two metal rings (cell crowns). Another option is to culture the cell-seeded SIS-Muc in a flow bioreactor system that exposes the cells to shear stress. Here, the bioreactor is connected to a peristaltic pump in a self-constructed incubator. A computer regulates the arterial oxygen and nutrient supply via parameters such as blood pressure, temperature, and flow rate. This setup allows for a dynamic culture with either pressure-regulated pulsatile or constant flow. In this study, we could successfully establish both a static and dynamic 3D culture system for MPNSTs. The ability to model cancer tumors in a more natural 3D environment will enable the discovery, testing, and validation of future pharmaceuticals in a human-like model. MyJove Corporation 2013-08-06 /pmc/articles/PMC3846813/ /pubmed/23963401 http://dx.doi.org/10.3791/50460 Text en Copyright © 2013, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Cancer Biology
Moll, Corinna
Reboredo, Jenny
Schwarz, Thomas
Appelt, Antje
Schürlein, Sebastian
Walles, Heike
Nietzer, Sarah
Tissue Engineering of a Human 3D in vitro Tumor Test System
title Tissue Engineering of a Human 3D in vitro Tumor Test System
title_full Tissue Engineering of a Human 3D in vitro Tumor Test System
title_fullStr Tissue Engineering of a Human 3D in vitro Tumor Test System
title_full_unstemmed Tissue Engineering of a Human 3D in vitro Tumor Test System
title_short Tissue Engineering of a Human 3D in vitro Tumor Test System
title_sort tissue engineering of a human 3d in vitro tumor test system
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846813/
https://www.ncbi.nlm.nih.gov/pubmed/23963401
http://dx.doi.org/10.3791/50460
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