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Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

BACKGROUND: Malignant mesothelioma (MM) is a rare aggressive cancer primary located in pleura and lung. MMs can be divided into biphasic, epithelioid and sarcomatoid subtypes. In majority of cases MMs are induced by asbestos fiber exposure. As latency period after asbestos exposure ranges between ~ ...

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Autores principales: Wahlbuhl, Eva, Liehr, Thomas, Rincic, Martina, Azawi, Shaymaa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488062/
https://www.ncbi.nlm.nih.gov/pubmed/32944078
http://dx.doi.org/10.1186/s13039-020-00511-4
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author Wahlbuhl, Eva
Liehr, Thomas
Rincic, Martina
Azawi, Shaymaa
author_facet Wahlbuhl, Eva
Liehr, Thomas
Rincic, Martina
Azawi, Shaymaa
author_sort Wahlbuhl, Eva
collection PubMed
description BACKGROUND: Malignant mesothelioma (MM) is a rare aggressive cancer primary located in pleura and lung. MMs can be divided into biphasic, epithelioid and sarcomatoid subtypes. In majority of cases MMs are induced by asbestos fiber exposure. As latency period after asbestos exposure ranges between ~ 10 and 60 years MMs are mainly observed in elder people. Human MM, being a rare tumor type, lacks detailed cytogenetic data, while molecular genetic studies have been undertaken more frequently. However, murine MM cell lines are also regularly applied to get more insight into MM biology and to test new therapy strategies. RESULTS: Here the murine MM cell lines AB1, AB22 and AC29 were studied by molecular cytogenetics and molecular karyotyping. Interestingly, yet there were no genetic or genomic studies undertaken for these already in 1992 established cell lines. The obtained data on genomic imbalances in these murine cell lines was translated into the human genome as previously reported based on human and murine genomic browsers. CONCLUSIONS: It turned out that all three cell lines showed high similarities in copy number variants as observed typically in human MM. Also, all three cell lines were most similar to human epithelioid MMs, and should be used as models therefore. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13039-020-00511-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-74880622020-09-16 Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines Wahlbuhl, Eva Liehr, Thomas Rincic, Martina Azawi, Shaymaa Mol Cytogenet Research BACKGROUND: Malignant mesothelioma (MM) is a rare aggressive cancer primary located in pleura and lung. MMs can be divided into biphasic, epithelioid and sarcomatoid subtypes. In majority of cases MMs are induced by asbestos fiber exposure. As latency period after asbestos exposure ranges between ~ 10 and 60 years MMs are mainly observed in elder people. Human MM, being a rare tumor type, lacks detailed cytogenetic data, while molecular genetic studies have been undertaken more frequently. However, murine MM cell lines are also regularly applied to get more insight into MM biology and to test new therapy strategies. RESULTS: Here the murine MM cell lines AB1, AB22 and AC29 were studied by molecular cytogenetics and molecular karyotyping. Interestingly, yet there were no genetic or genomic studies undertaken for these already in 1992 established cell lines. The obtained data on genomic imbalances in these murine cell lines was translated into the human genome as previously reported based on human and murine genomic browsers. CONCLUSIONS: It turned out that all three cell lines showed high similarities in copy number variants as observed typically in human MM. Also, all three cell lines were most similar to human epithelioid MMs, and should be used as models therefore. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13039-020-00511-4) contains supplementary material, which is available to authorized users. BioMed Central 2020-09-09 /pmc/articles/PMC7488062/ /pubmed/32944078 http://dx.doi.org/10.1186/s13039-020-00511-4 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Wahlbuhl, Eva
Liehr, Thomas
Rincic, Martina
Azawi, Shaymaa
Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines
title Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines
title_full Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines
title_fullStr Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines
title_full_unstemmed Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines
title_short Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines
title_sort cytogenomic characterization of three murine malignant mesothelioma tumor cell lines
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488062/
https://www.ncbi.nlm.nih.gov/pubmed/32944078
http://dx.doi.org/10.1186/s13039-020-00511-4
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