Cargando…

Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft

The role of stroma is fundamental in the development and behavior of epithelial tumors. In this regard, limited growth of squamous cell carcinomas (SCC) or cell-lines derived from them has been achieved in immunodeficient mice. Moreover, lack of faithful recapitulation of the original human neoplasi...

Descripción completa

Detalles Bibliográficos
Autores principales: Guerrero-Aspizua, Sara, González-Masa, Andrea, Conti, Claudio J., García, Marta, Chacón-Solano, Esteban, Larcher, Fernando, del Río, Marcela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139348/
https://www.ncbi.nlm.nih.gov/pubmed/32178458
http://dx.doi.org/10.3390/ijms21061951
_version_ 1783518745216417792
author Guerrero-Aspizua, Sara
González-Masa, Andrea
Conti, Claudio J.
García, Marta
Chacón-Solano, Esteban
Larcher, Fernando
del Río, Marcela
author_facet Guerrero-Aspizua, Sara
González-Masa, Andrea
Conti, Claudio J.
García, Marta
Chacón-Solano, Esteban
Larcher, Fernando
del Río, Marcela
author_sort Guerrero-Aspizua, Sara
collection PubMed
description The role of stroma is fundamental in the development and behavior of epithelial tumors. In this regard, limited growth of squamous cell carcinomas (SCC) or cell-lines derived from them has been achieved in immunodeficient mice. Moreover, lack of faithful recapitulation of the original human neoplasia complexity is often observed in xenografted tumors. Here, we used tissue engineering techniques to recreate a humanized tumor stroma for SCCs grafted in host mice, by combining CAF (cancer associated fibroblasts)-like cells with a biocompatible scaffold. The stroma was either co-injected with epithelial cell lines derived from aggressive SCC or implanted 15 days before the injection of the tumoral cells, to allow its vascularization and maturation. None of the mice injected with the cell lines without stroma were able to develop a SCC. In contrast, tumors were able to grow when SCC cells were injected into previously established humanized stroma. Histologically, all of the regenerated tumors were moderately differentiated SCC with a well-developed stroma, resembling that found in the original human neoplasm. Persistence of human stromal cells was also confirmed by immunohistochemistry. In summary, we provide a proof of concept that humanized tumor stroma, generated by tissue engineering, can facilitate the development of epithelial tumors in immunodeficient mice.
format Online
Article
Text
id pubmed-7139348
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-71393482020-04-10 Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft Guerrero-Aspizua, Sara González-Masa, Andrea Conti, Claudio J. García, Marta Chacón-Solano, Esteban Larcher, Fernando del Río, Marcela Int J Mol Sci Article The role of stroma is fundamental in the development and behavior of epithelial tumors. In this regard, limited growth of squamous cell carcinomas (SCC) or cell-lines derived from them has been achieved in immunodeficient mice. Moreover, lack of faithful recapitulation of the original human neoplasia complexity is often observed in xenografted tumors. Here, we used tissue engineering techniques to recreate a humanized tumor stroma for SCCs grafted in host mice, by combining CAF (cancer associated fibroblasts)-like cells with a biocompatible scaffold. The stroma was either co-injected with epithelial cell lines derived from aggressive SCC or implanted 15 days before the injection of the tumoral cells, to allow its vascularization and maturation. None of the mice injected with the cell lines without stroma were able to develop a SCC. In contrast, tumors were able to grow when SCC cells were injected into previously established humanized stroma. Histologically, all of the regenerated tumors were moderately differentiated SCC with a well-developed stroma, resembling that found in the original human neoplasm. Persistence of human stromal cells was also confirmed by immunohistochemistry. In summary, we provide a proof of concept that humanized tumor stroma, generated by tissue engineering, can facilitate the development of epithelial tumors in immunodeficient mice. MDPI 2020-03-12 /pmc/articles/PMC7139348/ /pubmed/32178458 http://dx.doi.org/10.3390/ijms21061951 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Guerrero-Aspizua, Sara
González-Masa, Andrea
Conti, Claudio J.
García, Marta
Chacón-Solano, Esteban
Larcher, Fernando
del Río, Marcela
Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft
title Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft
title_full Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft
title_fullStr Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft
title_full_unstemmed Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft
title_short Humanization of Tumor Stroma by Tissue Engineering as a Tool to Improve Squamous Cell Carcinoma Xenograft
title_sort humanization of tumor stroma by tissue engineering as a tool to improve squamous cell carcinoma xenograft
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139348/
https://www.ncbi.nlm.nih.gov/pubmed/32178458
http://dx.doi.org/10.3390/ijms21061951
work_keys_str_mv AT guerreroaspizuasara humanizationoftumorstromabytissueengineeringasatooltoimprovesquamouscellcarcinomaxenograft
AT gonzalezmasaandrea humanizationoftumorstromabytissueengineeringasatooltoimprovesquamouscellcarcinomaxenograft
AT conticlaudioj humanizationoftumorstromabytissueengineeringasatooltoimprovesquamouscellcarcinomaxenograft
AT garciamarta humanizationoftumorstromabytissueengineeringasatooltoimprovesquamouscellcarcinomaxenograft
AT chaconsolanoesteban humanizationoftumorstromabytissueengineeringasatooltoimprovesquamouscellcarcinomaxenograft
AT larcherfernando humanizationoftumorstromabytissueengineeringasatooltoimprovesquamouscellcarcinomaxenograft
AT delriomarcela humanizationoftumorstromabytissueengineeringasatooltoimprovesquamouscellcarcinomaxenograft