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Extracellular matrix stiffness mediates radiosensitivity in a 3D nasopharyngeal carcinoma model

PURPOSE: Radiotherapy is one of the essential treatment modalities for nasopharyngeal carcinoma (NPC), however, radioresistance still poses challenges. Three-dimensional (3D) tumor culture models mimic the in vivo growth conditions of cells more accurately than 2D models. This study is to compare th...

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Autores principales: Fang, Yanhua, Liang, Shanshan, Gao, Jianong, Wang, Zhe, Li, Cheng, Wang, Ruoyu, Yu, Weiting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675143/
https://www.ncbi.nlm.nih.gov/pubmed/36403050
http://dx.doi.org/10.1186/s12935-022-02787-5
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author Fang, Yanhua
Liang, Shanshan
Gao, Jianong
Wang, Zhe
Li, Cheng
Wang, Ruoyu
Yu, Weiting
author_facet Fang, Yanhua
Liang, Shanshan
Gao, Jianong
Wang, Zhe
Li, Cheng
Wang, Ruoyu
Yu, Weiting
author_sort Fang, Yanhua
collection PubMed
description PURPOSE: Radiotherapy is one of the essential treatment modalities for nasopharyngeal carcinoma (NPC), however, radioresistance still poses challenges. Three-dimensional (3D) tumor culture models mimic the in vivo growth conditions of cells more accurately than 2D models. This study is to compare the tumor biological behaviors of NPC cells in 2D, On-Surface 3D and Embedded 3D systems, and to investigate the correlation between radioresistance and extracellular matrix (ECM) stiffness. METHODS: The morphology and radioresistance of the human NPC cell line CNE-1 were observed in 2D and 3D systems. The CCK-8 assay, wounding healing assays, flow cytometry, soft agar assays, and western blot analysis were used to evaluate differences in biological behaviors such as proliferation, migration, cell cycle distribution, and stem cell activity. Different ECM stiffness systems were established by co-blending collagen and alginate in varying proportions. ECM stiffness was evaluated by compressive elastic moduli measurement and colony formation assay was used to assess radioresistance of NPC cells in systems with different ECM stiffness after irradiation. RESULTS: Compared to 2D models, the morphology of NPC cells in 3D culture microenvironments has more in common with in vivo tumor cells and 3D cultured NPC cells exhibit stronger radioresistance. Integrin β1 but not the epithelial-to-mesenchymal transition pathway in 3D models boost migration ability. Cell proliferation was enhanced, the proportion of tumor stem cells was increased, and G1/S phase arrest occurred in 3D models. NPC cells cultured in softer ECM systems (with low alginate proportions) exhibit striking resistance to ionizing radiation. CONCLUSION: The tumor biological behaviors of NPC cells in 3D groups were obviously different from that of 2D. Radioresistance of NPC cells increased with the stiffness of ECM decreasing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02787-5.
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spelling pubmed-96751432022-11-20 Extracellular matrix stiffness mediates radiosensitivity in a 3D nasopharyngeal carcinoma model Fang, Yanhua Liang, Shanshan Gao, Jianong Wang, Zhe Li, Cheng Wang, Ruoyu Yu, Weiting Cancer Cell Int Research PURPOSE: Radiotherapy is one of the essential treatment modalities for nasopharyngeal carcinoma (NPC), however, radioresistance still poses challenges. Three-dimensional (3D) tumor culture models mimic the in vivo growth conditions of cells more accurately than 2D models. This study is to compare the tumor biological behaviors of NPC cells in 2D, On-Surface 3D and Embedded 3D systems, and to investigate the correlation between radioresistance and extracellular matrix (ECM) stiffness. METHODS: The morphology and radioresistance of the human NPC cell line CNE-1 were observed in 2D and 3D systems. The CCK-8 assay, wounding healing assays, flow cytometry, soft agar assays, and western blot analysis were used to evaluate differences in biological behaviors such as proliferation, migration, cell cycle distribution, and stem cell activity. Different ECM stiffness systems were established by co-blending collagen and alginate in varying proportions. ECM stiffness was evaluated by compressive elastic moduli measurement and colony formation assay was used to assess radioresistance of NPC cells in systems with different ECM stiffness after irradiation. RESULTS: Compared to 2D models, the morphology of NPC cells in 3D culture microenvironments has more in common with in vivo tumor cells and 3D cultured NPC cells exhibit stronger radioresistance. Integrin β1 but not the epithelial-to-mesenchymal transition pathway in 3D models boost migration ability. Cell proliferation was enhanced, the proportion of tumor stem cells was increased, and G1/S phase arrest occurred in 3D models. NPC cells cultured in softer ECM systems (with low alginate proportions) exhibit striking resistance to ionizing radiation. CONCLUSION: The tumor biological behaviors of NPC cells in 3D groups were obviously different from that of 2D. Radioresistance of NPC cells increased with the stiffness of ECM decreasing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02787-5. BioMed Central 2022-11-19 /pmc/articles/PMC9675143/ /pubmed/36403050 http://dx.doi.org/10.1186/s12935-022-02787-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Fang, Yanhua
Liang, Shanshan
Gao, Jianong
Wang, Zhe
Li, Cheng
Wang, Ruoyu
Yu, Weiting
Extracellular matrix stiffness mediates radiosensitivity in a 3D nasopharyngeal carcinoma model
title Extracellular matrix stiffness mediates radiosensitivity in a 3D nasopharyngeal carcinoma model
title_full Extracellular matrix stiffness mediates radiosensitivity in a 3D nasopharyngeal carcinoma model
title_fullStr Extracellular matrix stiffness mediates radiosensitivity in a 3D nasopharyngeal carcinoma model
title_full_unstemmed Extracellular matrix stiffness mediates radiosensitivity in a 3D nasopharyngeal carcinoma model
title_short Extracellular matrix stiffness mediates radiosensitivity in a 3D nasopharyngeal carcinoma model
title_sort extracellular matrix stiffness mediates radiosensitivity in a 3d nasopharyngeal carcinoma model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675143/
https://www.ncbi.nlm.nih.gov/pubmed/36403050
http://dx.doi.org/10.1186/s12935-022-02787-5
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