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Phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog
Canine pulmonary adenocarcinoma (PAC) resembles human lung tumors in never-smokers, but it is rarer than human pulmonary adenocarcinoma. Therefore, research on canine PAC is challenging. In the present study, we successfully established various novel canine PAC cell lines from a single lesion in a d...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556002/ https://www.ncbi.nlm.nih.gov/pubmed/37798461 http://dx.doi.org/10.1038/s41598-023-44062-1 |
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author | Kobayashi, Kosuke Takemura, Reika Deja Miyamae, Jiro Mitsui, Ikki Murakami, Kohei Kutara, Kenji Saeki, Kohei Kanda, Teppei Okamura, Yasuhiko Sugiyama, Akihiko |
author_facet | Kobayashi, Kosuke Takemura, Reika Deja Miyamae, Jiro Mitsui, Ikki Murakami, Kohei Kutara, Kenji Saeki, Kohei Kanda, Teppei Okamura, Yasuhiko Sugiyama, Akihiko |
author_sort | Kobayashi, Kosuke |
collection | PubMed |
description | Canine pulmonary adenocarcinoma (PAC) resembles human lung tumors in never-smokers, but it is rarer than human pulmonary adenocarcinoma. Therefore, research on canine PAC is challenging. In the present study, we successfully established various novel canine PAC cell lines from a single lesion in a dog, including two parent cell lines and fourteen cloned cell lines, and characterized their cellular properties in vitro. Several of these cell lines showed epithelial–mesenchymal transition (EMT)-like and/or cancer stem cell (CSCs)-like phenotypes. We additionally assessed the sensitivity of the cells to vinorelbine in vitro. Three clonal lines, two of which showed EMT- and CSC-like phenotypes, were resistant to vinorelbine. Furthermore, we evaluated the expression and activation status of EGFR, HER2, and Ras signaling factors. The findings indicated that the cell lines we established preserved the expression and activation of these factors to varying extents. These novel canine PAC cell lines can be utilized in future research for understanding the pathogenesis and development of treatments for canine PAC. |
format | Online Article Text |
id | pubmed-10556002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105560022023-10-07 Phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog Kobayashi, Kosuke Takemura, Reika Deja Miyamae, Jiro Mitsui, Ikki Murakami, Kohei Kutara, Kenji Saeki, Kohei Kanda, Teppei Okamura, Yasuhiko Sugiyama, Akihiko Sci Rep Article Canine pulmonary adenocarcinoma (PAC) resembles human lung tumors in never-smokers, but it is rarer than human pulmonary adenocarcinoma. Therefore, research on canine PAC is challenging. In the present study, we successfully established various novel canine PAC cell lines from a single lesion in a dog, including two parent cell lines and fourteen cloned cell lines, and characterized their cellular properties in vitro. Several of these cell lines showed epithelial–mesenchymal transition (EMT)-like and/or cancer stem cell (CSCs)-like phenotypes. We additionally assessed the sensitivity of the cells to vinorelbine in vitro. Three clonal lines, two of which showed EMT- and CSC-like phenotypes, were resistant to vinorelbine. Furthermore, we evaluated the expression and activation status of EGFR, HER2, and Ras signaling factors. The findings indicated that the cell lines we established preserved the expression and activation of these factors to varying extents. These novel canine PAC cell lines can be utilized in future research for understanding the pathogenesis and development of treatments for canine PAC. Nature Publishing Group UK 2023-10-05 /pmc/articles/PMC10556002/ /pubmed/37798461 http://dx.doi.org/10.1038/s41598-023-44062-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/) . |
spellingShingle | Article Kobayashi, Kosuke Takemura, Reika Deja Miyamae, Jiro Mitsui, Ikki Murakami, Kohei Kutara, Kenji Saeki, Kohei Kanda, Teppei Okamura, Yasuhiko Sugiyama, Akihiko Phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog |
title | Phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog |
title_full | Phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog |
title_fullStr | Phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog |
title_full_unstemmed | Phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog |
title_short | Phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog |
title_sort | phenotypic and molecular characterization of novel pulmonary adenocarcinoma cell lines established from a dog |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556002/ https://www.ncbi.nlm.nih.gov/pubmed/37798461 http://dx.doi.org/10.1038/s41598-023-44062-1 |
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