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Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells
The EGFR pathway plays a critical role in head and neck squamous cell carcinoma (HNSCC). Targeted therapies against the EGFR are utilized as a treatment for HNSCCC. However, patient response is heterogeneous and molecular biomarkers are lacking to predict patient response. Therefore, functional assa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713778/ https://www.ncbi.nlm.nih.gov/pubmed/31462653 http://dx.doi.org/10.1038/s41598-019-48764-3 |
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author | Ayuso, Jose M. Vitek, Ross Swick, Adam D. Skala, Melissa C. Wisinski, Kari B. Kimple, Randall J. Lambert, Paul F. Beebe, David J. |
author_facet | Ayuso, Jose M. Vitek, Ross Swick, Adam D. Skala, Melissa C. Wisinski, Kari B. Kimple, Randall J. Lambert, Paul F. Beebe, David J. |
author_sort | Ayuso, Jose M. |
collection | PubMed |
description | The EGFR pathway plays a critical role in head and neck squamous cell carcinoma (HNSCC). Targeted therapies against the EGFR are utilized as a treatment for HNSCCC. However, patient response is heterogeneous and molecular biomarkers are lacking to predict patient response. Therefore, functional assays where drug response is directly evaluated in tumor cells are an interesting alternative. Previous studies have shown that experimental conditions modify the drug response observed in functional assays. Thus, in this work the influence of the culture environment on response to Cetuximab (EGFR monoclonal antibody) and AZD8055 (mTOR inhibitor) was evaluated. HNSCC UM-SCC-1 and UM-SCC-47 cells were cultured in 2D monoculture and compared with: 2D co-culture with cancer-associated fibroblasts (CAF); 3D culture in collagen hydrogels; and 3D culture in tumor spheroids. The results showed UM-SCC-1 drug response significantly changed in the different culture environments; leading to an increase in drug resistance in the CAF co-culture and the 3D spheroids. Conversely, UM-SCC-47 exhibited a more constant drug response across culture conditions. In conclusion, this work highlights the importance of culture conditions that modulate response to EGFR pathway inhibition. |
format | Online Article Text |
id | pubmed-6713778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67137782019-09-13 Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells Ayuso, Jose M. Vitek, Ross Swick, Adam D. Skala, Melissa C. Wisinski, Kari B. Kimple, Randall J. Lambert, Paul F. Beebe, David J. Sci Rep Article The EGFR pathway plays a critical role in head and neck squamous cell carcinoma (HNSCC). Targeted therapies against the EGFR are utilized as a treatment for HNSCCC. However, patient response is heterogeneous and molecular biomarkers are lacking to predict patient response. Therefore, functional assays where drug response is directly evaluated in tumor cells are an interesting alternative. Previous studies have shown that experimental conditions modify the drug response observed in functional assays. Thus, in this work the influence of the culture environment on response to Cetuximab (EGFR monoclonal antibody) and AZD8055 (mTOR inhibitor) was evaluated. HNSCC UM-SCC-1 and UM-SCC-47 cells were cultured in 2D monoculture and compared with: 2D co-culture with cancer-associated fibroblasts (CAF); 3D culture in collagen hydrogels; and 3D culture in tumor spheroids. The results showed UM-SCC-1 drug response significantly changed in the different culture environments; leading to an increase in drug resistance in the CAF co-culture and the 3D spheroids. Conversely, UM-SCC-47 exhibited a more constant drug response across culture conditions. In conclusion, this work highlights the importance of culture conditions that modulate response to EGFR pathway inhibition. Nature Publishing Group UK 2019-08-28 /pmc/articles/PMC6713778/ /pubmed/31462653 http://dx.doi.org/10.1038/s41598-019-48764-3 Text en © The Author(s) 2019 Open Access 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 http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ayuso, Jose M. Vitek, Ross Swick, Adam D. Skala, Melissa C. Wisinski, Kari B. Kimple, Randall J. Lambert, Paul F. Beebe, David J. Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells |
title | Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells |
title_full | Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells |
title_fullStr | Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells |
title_full_unstemmed | Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells |
title_short | Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells |
title_sort | effects of culture method on response to egfr therapy in head and neck squamous cell carcinoma cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713778/ https://www.ncbi.nlm.nih.gov/pubmed/31462653 http://dx.doi.org/10.1038/s41598-019-48764-3 |
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