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Patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments
Malignant pleural mesothelioma (MPM) is an aggressive cancer, associated with poor prognosis. We assessed the feasibility of patient-derived cell cultures to serve as an ex vivo model of MPM. Patient-derived MPM cell cultures (n=16) exhibited stemness features and reflected intratumour and interpati...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569377/ https://www.ncbi.nlm.nih.gov/pubmed/32943495 http://dx.doi.org/10.1136/thoraxjnl-2020-215027 |
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author | Kanellakis, Nikolaos I Asciak, Rachelle Hamid, Megat Abd Yao, Xuan McCole, Mark McGowan, Simon Seraia, Elena Hatch, Stephanie Hallifax, Rob J Mercer, Rachel M Bedawi, Eihab O Jones, Stephanie Verrill, Clare Dobson, Melissa George, Vineeth Stathopoulos, Georgios T Peng, Yanchun Ebner, Daniel Dong, Tao Rahman, Najib M Psallidas, Ioannis |
author_facet | Kanellakis, Nikolaos I Asciak, Rachelle Hamid, Megat Abd Yao, Xuan McCole, Mark McGowan, Simon Seraia, Elena Hatch, Stephanie Hallifax, Rob J Mercer, Rachel M Bedawi, Eihab O Jones, Stephanie Verrill, Clare Dobson, Melissa George, Vineeth Stathopoulos, Georgios T Peng, Yanchun Ebner, Daniel Dong, Tao Rahman, Najib M Psallidas, Ioannis |
author_sort | Kanellakis, Nikolaos I |
collection | PubMed |
description | Malignant pleural mesothelioma (MPM) is an aggressive cancer, associated with poor prognosis. We assessed the feasibility of patient-derived cell cultures to serve as an ex vivo model of MPM. Patient-derived MPM cell cultures (n=16) exhibited stemness features and reflected intratumour and interpatient heterogeneity. A subset of the cells were subjected to high-throughput drug screening and coculture assays with cancer-specific cytotoxic T cells and showed diverse responses. Some of the biphasic MPM cells were capable of processing and presenting the neoantigen SSX-2 endogenously. In conclusion, patient-derived MPM cell cultures are a promising and faithful ex vivo model of MPM. |
format | Online Article Text |
id | pubmed-7569377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-75693772020-10-20 Patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments Kanellakis, Nikolaos I Asciak, Rachelle Hamid, Megat Abd Yao, Xuan McCole, Mark McGowan, Simon Seraia, Elena Hatch, Stephanie Hallifax, Rob J Mercer, Rachel M Bedawi, Eihab O Jones, Stephanie Verrill, Clare Dobson, Melissa George, Vineeth Stathopoulos, Georgios T Peng, Yanchun Ebner, Daniel Dong, Tao Rahman, Najib M Psallidas, Ioannis Thorax Brief Communication Malignant pleural mesothelioma (MPM) is an aggressive cancer, associated with poor prognosis. We assessed the feasibility of patient-derived cell cultures to serve as an ex vivo model of MPM. Patient-derived MPM cell cultures (n=16) exhibited stemness features and reflected intratumour and interpatient heterogeneity. A subset of the cells were subjected to high-throughput drug screening and coculture assays with cancer-specific cytotoxic T cells and showed diverse responses. Some of the biphasic MPM cells were capable of processing and presenting the neoantigen SSX-2 endogenously. In conclusion, patient-derived MPM cell cultures are a promising and faithful ex vivo model of MPM. BMJ Publishing Group 2020-11 2020-09-17 /pmc/articles/PMC7569377/ /pubmed/32943495 http://dx.doi.org/10.1136/thoraxjnl-2020-215027 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Brief Communication Kanellakis, Nikolaos I Asciak, Rachelle Hamid, Megat Abd Yao, Xuan McCole, Mark McGowan, Simon Seraia, Elena Hatch, Stephanie Hallifax, Rob J Mercer, Rachel M Bedawi, Eihab O Jones, Stephanie Verrill, Clare Dobson, Melissa George, Vineeth Stathopoulos, Georgios T Peng, Yanchun Ebner, Daniel Dong, Tao Rahman, Najib M Psallidas, Ioannis Patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments |
title | Patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments |
title_full | Patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments |
title_fullStr | Patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments |
title_full_unstemmed | Patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments |
title_short | Patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments |
title_sort | patient-derived malignant pleural mesothelioma cell cultures: a tool to advance biomarker-driven treatments |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569377/ https://www.ncbi.nlm.nih.gov/pubmed/32943495 http://dx.doi.org/10.1136/thoraxjnl-2020-215027 |
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