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Development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma

BACKGROUND: Current organotypic models of dysplasia and oral squamous cell carcinoma (OSCC) lack the complexity that mimics in vivo tissue. Here we describe a three-dimensional in vitro model of the oral epithelium that replicates tumour progression from dysplasia to an invasive phenotype. METHODS:...

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Autores principales: Colley, H E, Hearnden, V, Jones, A V, Weinreb, P H, Violette, S M, MacNeil, S, Thornhill, M H, Murdoch, C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3242522/
https://www.ncbi.nlm.nih.gov/pubmed/21989184
http://dx.doi.org/10.1038/bjc.2011.403
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author Colley, H E
Hearnden, V
Jones, A V
Weinreb, P H
Violette, S M
MacNeil, S
Thornhill, M H
Murdoch, C
author_facet Colley, H E
Hearnden, V
Jones, A V
Weinreb, P H
Violette, S M
MacNeil, S
Thornhill, M H
Murdoch, C
author_sort Colley, H E
collection PubMed
description BACKGROUND: Current organotypic models of dysplasia and oral squamous cell carcinoma (OSCC) lack the complexity that mimics in vivo tissue. Here we describe a three-dimensional in vitro model of the oral epithelium that replicates tumour progression from dysplasia to an invasive phenotype. METHODS: The OSCC cell lines were seeded as a cell suspension (D20, Cal27) or as multicellular tumour spheroids (FaDu) with oral fibroblasts on to a de-epidermised acellular dermis to generate tissue-engineered models and compared with patient biopsies. RESULTS: The D20 and Cal27 cells generated a model of epithelial dysplasia. Overtime Cal27 cells traversed the basement membrane and invaded the connective tissue to reproduce features of early invasive OSCC. When seeded onto a model of the normal oral mucosa, FaDu spheroids produced a histological picture mimicking carcinoma in situ with severe cellular atypia juxtaposed to normal epithelium. CONCLUSION: It is possible to culture in vitro models with the morphological appearance and histological characteristics of dysplasia and tumour cell invasion seen in vivo using native dermis. Such models could facilitate study of the molecular processes involved in malignant transformation, invasion and tumour growth as well as in vitro testing of new treatments, diagnostic tests and drug delivery systems for OSCC.
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spelling pubmed-32425222012-11-08 Development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma Colley, H E Hearnden, V Jones, A V Weinreb, P H Violette, S M MacNeil, S Thornhill, M H Murdoch, C Br J Cancer Molecular Diagnostics BACKGROUND: Current organotypic models of dysplasia and oral squamous cell carcinoma (OSCC) lack the complexity that mimics in vivo tissue. Here we describe a three-dimensional in vitro model of the oral epithelium that replicates tumour progression from dysplasia to an invasive phenotype. METHODS: The OSCC cell lines were seeded as a cell suspension (D20, Cal27) or as multicellular tumour spheroids (FaDu) with oral fibroblasts on to a de-epidermised acellular dermis to generate tissue-engineered models and compared with patient biopsies. RESULTS: The D20 and Cal27 cells generated a model of epithelial dysplasia. Overtime Cal27 cells traversed the basement membrane and invaded the connective tissue to reproduce features of early invasive OSCC. When seeded onto a model of the normal oral mucosa, FaDu spheroids produced a histological picture mimicking carcinoma in situ with severe cellular atypia juxtaposed to normal epithelium. CONCLUSION: It is possible to culture in vitro models with the morphological appearance and histological characteristics of dysplasia and tumour cell invasion seen in vivo using native dermis. Such models could facilitate study of the molecular processes involved in malignant transformation, invasion and tumour growth as well as in vitro testing of new treatments, diagnostic tests and drug delivery systems for OSCC. Nature Publishing Group 2011-11-08 2011-10-11 /pmc/articles/PMC3242522/ /pubmed/21989184 http://dx.doi.org/10.1038/bjc.2011.403 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Colley, H E
Hearnden, V
Jones, A V
Weinreb, P H
Violette, S M
MacNeil, S
Thornhill, M H
Murdoch, C
Development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma
title Development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma
title_full Development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma
title_fullStr Development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma
title_full_unstemmed Development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma
title_short Development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma
title_sort development of tissue-engineered models of oral dysplasia and early invasive oral squamous cell carcinoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3242522/
https://www.ncbi.nlm.nih.gov/pubmed/21989184
http://dx.doi.org/10.1038/bjc.2011.403
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