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Development of an in vitro cell-sheet cancer model for chemotherapeutic screening

Epithelial cancer grows in vivo in a microenvironment that comprises tumour, stroma, and immune cells. A three-dimensional (3D) culture model might be able to mimic the tumour microenvironment in vivo; therefore, we developed a new 3D epithelial cancer model using in vitro cell-sheet engineering and...

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Autores principales: Lee, Jaewang, Shin, Daiha, Roh, Jong-Lyel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071526/
https://www.ncbi.nlm.nih.gov/pubmed/30083273
http://dx.doi.org/10.7150/thno.26439
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author Lee, Jaewang
Shin, Daiha
Roh, Jong-Lyel
author_facet Lee, Jaewang
Shin, Daiha
Roh, Jong-Lyel
author_sort Lee, Jaewang
collection PubMed
description Epithelial cancer grows in vivo in a microenvironment that comprises tumour, stroma, and immune cells. A three-dimensional (3D) culture model might be able to mimic the tumour microenvironment in vivo; therefore, we developed a new 3D epithelial cancer model using in vitro cell-sheet engineering and compared the results of treatment with several chemotherapeutic drugs among the 3D cell-sheet model, spheroid culture, and 2D cell culture. Methods: The cell sheet comprised keratinocytes and a plasma fibrin matrix containing fibroblasts. Cancer spheroids with or without cancer-associated fibroblasts (CAFs) were interposed between the keratinocytes and fibrin layer. Cell growth, viability, and hypoxia were measured using the cell counting kit-8, LIVE/DEAD assay, and propidium iodide and LOX-1 staining. The morphology, invasion, and mRNA and protein expression were compared among the different cell culture models. Results: Enhanced resistance to sorafenib and cisplatin by cancer spheroids and CAFs was more easily observed in the 3D than in the 2D model. Invasion by cancer-CAF spheroids into the fibrin matrix was more clearly observed in the 3D cell sheet. The expansion of viable cancer cells increased in the 3D cell sheet, particularly in those with CAFs, which were significantly inhibited by treatment with 10 μM sorafenib or 20 μM cisplatin (P < 0.05). TGF-β1, N-cadherin, and vimentin mRNA and protein levels were higher in the 3D cell-sheet model. Conclusions: The 3D cell sheet-based cancer model could be applied to in vitro observation of epithelial cancer growth and invasion and to anticancer drug testing.
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spelling pubmed-60715262018-08-06 Development of an in vitro cell-sheet cancer model for chemotherapeutic screening Lee, Jaewang Shin, Daiha Roh, Jong-Lyel Theranostics Research Paper Epithelial cancer grows in vivo in a microenvironment that comprises tumour, stroma, and immune cells. A three-dimensional (3D) culture model might be able to mimic the tumour microenvironment in vivo; therefore, we developed a new 3D epithelial cancer model using in vitro cell-sheet engineering and compared the results of treatment with several chemotherapeutic drugs among the 3D cell-sheet model, spheroid culture, and 2D cell culture. Methods: The cell sheet comprised keratinocytes and a plasma fibrin matrix containing fibroblasts. Cancer spheroids with or without cancer-associated fibroblasts (CAFs) were interposed between the keratinocytes and fibrin layer. Cell growth, viability, and hypoxia were measured using the cell counting kit-8, LIVE/DEAD assay, and propidium iodide and LOX-1 staining. The morphology, invasion, and mRNA and protein expression were compared among the different cell culture models. Results: Enhanced resistance to sorafenib and cisplatin by cancer spheroids and CAFs was more easily observed in the 3D than in the 2D model. Invasion by cancer-CAF spheroids into the fibrin matrix was more clearly observed in the 3D cell sheet. The expansion of viable cancer cells increased in the 3D cell sheet, particularly in those with CAFs, which were significantly inhibited by treatment with 10 μM sorafenib or 20 μM cisplatin (P < 0.05). TGF-β1, N-cadherin, and vimentin mRNA and protein levels were higher in the 3D cell-sheet model. Conclusions: The 3D cell sheet-based cancer model could be applied to in vitro observation of epithelial cancer growth and invasion and to anticancer drug testing. Ivyspring International Publisher 2018-06-24 /pmc/articles/PMC6071526/ /pubmed/30083273 http://dx.doi.org/10.7150/thno.26439 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Lee, Jaewang
Shin, Daiha
Roh, Jong-Lyel
Development of an in vitro cell-sheet cancer model for chemotherapeutic screening
title Development of an in vitro cell-sheet cancer model for chemotherapeutic screening
title_full Development of an in vitro cell-sheet cancer model for chemotherapeutic screening
title_fullStr Development of an in vitro cell-sheet cancer model for chemotherapeutic screening
title_full_unstemmed Development of an in vitro cell-sheet cancer model for chemotherapeutic screening
title_short Development of an in vitro cell-sheet cancer model for chemotherapeutic screening
title_sort development of an in vitro cell-sheet cancer model for chemotherapeutic screening
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071526/
https://www.ncbi.nlm.nih.gov/pubmed/30083273
http://dx.doi.org/10.7150/thno.26439
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