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Crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models

The crosstalk between immune cells, cancer cells, and extracellular vesicles (EVs) secreted by cancer cells remains poorly understood. We created three-dimensional (3D) cell culture models using human leiomyoma discs and Myogel to study the effects of immune cells on highly (HSC-3) and less (SCC-25)...

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Autores principales: Al-Samadi, Ahmed, Awad, Shady Adnan, Tuomainen, Katja, Zhao, Yue, Salem, Abdelhakim, Parikka, Mataleena, Salo, Tuula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601126/
https://www.ncbi.nlm.nih.gov/pubmed/28947958
http://dx.doi.org/10.18632/oncotarget.17768
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author Al-Samadi, Ahmed
Awad, Shady Adnan
Tuomainen, Katja
Zhao, Yue
Salem, Abdelhakim
Parikka, Mataleena
Salo, Tuula
author_facet Al-Samadi, Ahmed
Awad, Shady Adnan
Tuomainen, Katja
Zhao, Yue
Salem, Abdelhakim
Parikka, Mataleena
Salo, Tuula
author_sort Al-Samadi, Ahmed
collection PubMed
description The crosstalk between immune cells, cancer cells, and extracellular vesicles (EVs) secreted by cancer cells remains poorly understood. We created three-dimensional (3D) cell culture models using human leiomyoma discs and Myogel to study the effects of immune cells on highly (HSC-3) and less (SCC-25) invasive oral tongue squamous cell carcinoma (OTSCC) cell lines. Additionally, we studied the effects of EVs isolated from these cell lines on the cytotoxicity of CD8(+) T and NK cells isolated from three healthy donors. Our analysis included the effects of these EVs on innate immunity in zebrafish larvae. Activated immune cells significantly decreased the proliferation of both OTSCC cell lines and associated with a diminished invasion area of HSC-3 cells. In general, EVs from SCC-25 increased the cytotoxic activity of CD8(+) T and NK cells more than those from HSC-3 cells. However, this effect varied depending on the source and the immune and cancer cell subgroups. In zebrafish, the amount of IL-13 mRNA was decreased by SCC-25 EVs. This study describes promising in vitro and in vivo models to investigate interactions between immune cells, cancer cells, and EVs.
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spelling pubmed-56011262017-09-25 Crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models Al-Samadi, Ahmed Awad, Shady Adnan Tuomainen, Katja Zhao, Yue Salem, Abdelhakim Parikka, Mataleena Salo, Tuula Oncotarget Research Paper The crosstalk between immune cells, cancer cells, and extracellular vesicles (EVs) secreted by cancer cells remains poorly understood. We created three-dimensional (3D) cell culture models using human leiomyoma discs and Myogel to study the effects of immune cells on highly (HSC-3) and less (SCC-25) invasive oral tongue squamous cell carcinoma (OTSCC) cell lines. Additionally, we studied the effects of EVs isolated from these cell lines on the cytotoxicity of CD8(+) T and NK cells isolated from three healthy donors. Our analysis included the effects of these EVs on innate immunity in zebrafish larvae. Activated immune cells significantly decreased the proliferation of both OTSCC cell lines and associated with a diminished invasion area of HSC-3 cells. In general, EVs from SCC-25 increased the cytotoxic activity of CD8(+) T and NK cells more than those from HSC-3 cells. However, this effect varied depending on the source and the immune and cancer cell subgroups. In zebrafish, the amount of IL-13 mRNA was decreased by SCC-25 EVs. This study describes promising in vitro and in vivo models to investigate interactions between immune cells, cancer cells, and EVs. Impact Journals LLC 2017-05-10 /pmc/articles/PMC5601126/ /pubmed/28947958 http://dx.doi.org/10.18632/oncotarget.17768 Text en Copyright: © 2017 Al-Samadi et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Al-Samadi, Ahmed
Awad, Shady Adnan
Tuomainen, Katja
Zhao, Yue
Salem, Abdelhakim
Parikka, Mataleena
Salo, Tuula
Crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models
title Crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models
title_full Crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models
title_fullStr Crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models
title_full_unstemmed Crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models
title_short Crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models
title_sort crosstalk between tongue carcinoma cells, extracellular vesicles, and immune cells in in vitro and in vivo models
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601126/
https://www.ncbi.nlm.nih.gov/pubmed/28947958
http://dx.doi.org/10.18632/oncotarget.17768
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