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Reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer

Intratumoural heterogeneity (ITH) contributes to local recurrence following radiotherapy in prostate cancer. Recent studies also show that ecological interactions between heterogeneous tumour cell populations can lead to resistance in chemotherapy. Here, we evaluated whether interactions between het...

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Autores principales: Paczkowski, Marcin, Kretzschmar, Warren W., Markelc, Bostjan, Liu, Stanley K., Kunz-Schughart, Leoni A., Harris, Adrian L., Partridge, Mike, Byrne, Helen M., Kannan, Pavitra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782740/
https://www.ncbi.nlm.nih.gov/pubmed/33398023
http://dx.doi.org/10.1038/s42003-020-01529-5
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author Paczkowski, Marcin
Kretzschmar, Warren W.
Markelc, Bostjan
Liu, Stanley K.
Kunz-Schughart, Leoni A.
Harris, Adrian L.
Partridge, Mike
Byrne, Helen M.
Kannan, Pavitra
author_facet Paczkowski, Marcin
Kretzschmar, Warren W.
Markelc, Bostjan
Liu, Stanley K.
Kunz-Schughart, Leoni A.
Harris, Adrian L.
Partridge, Mike
Byrne, Helen M.
Kannan, Pavitra
author_sort Paczkowski, Marcin
collection PubMed
description Intratumoural heterogeneity (ITH) contributes to local recurrence following radiotherapy in prostate cancer. Recent studies also show that ecological interactions between heterogeneous tumour cell populations can lead to resistance in chemotherapy. Here, we evaluated whether interactions between heterogenous populations could impact growth and response to radiotherapy in prostate cancer. Using mixed 3D cultures of parental and radioresistant populations from two prostate cancer cell lines and a predator-prey mathematical model to investigate various types of ecological interactions, we show that reciprocal interactions between heterogeneous populations enhance overall growth and reduce radiation sensitivity. The type of interaction influences the time of regrowth after radiation, and, at the population level, alters the survival and cell cycle of each population without eliminating either one. These interactions can arise from oxygen constraints and from cellular cross-talk that alter the tumour microenvironment. These findings suggest that ecological-type interactions are important in radiation response and could be targeted to reduce local recurrence.
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spelling pubmed-77827402021-01-11 Reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer Paczkowski, Marcin Kretzschmar, Warren W. Markelc, Bostjan Liu, Stanley K. Kunz-Schughart, Leoni A. Harris, Adrian L. Partridge, Mike Byrne, Helen M. Kannan, Pavitra Commun Biol Article Intratumoural heterogeneity (ITH) contributes to local recurrence following radiotherapy in prostate cancer. Recent studies also show that ecological interactions between heterogeneous tumour cell populations can lead to resistance in chemotherapy. Here, we evaluated whether interactions between heterogenous populations could impact growth and response to radiotherapy in prostate cancer. Using mixed 3D cultures of parental and radioresistant populations from two prostate cancer cell lines and a predator-prey mathematical model to investigate various types of ecological interactions, we show that reciprocal interactions between heterogeneous populations enhance overall growth and reduce radiation sensitivity. The type of interaction influences the time of regrowth after radiation, and, at the population level, alters the survival and cell cycle of each population without eliminating either one. These interactions can arise from oxygen constraints and from cellular cross-talk that alter the tumour microenvironment. These findings suggest that ecological-type interactions are important in radiation response and could be targeted to reduce local recurrence. Nature Publishing Group UK 2021-01-04 /pmc/articles/PMC7782740/ /pubmed/33398023 http://dx.doi.org/10.1038/s42003-020-01529-5 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Paczkowski, Marcin
Kretzschmar, Warren W.
Markelc, Bostjan
Liu, Stanley K.
Kunz-Schughart, Leoni A.
Harris, Adrian L.
Partridge, Mike
Byrne, Helen M.
Kannan, Pavitra
Reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer
title Reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer
title_full Reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer
title_fullStr Reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer
title_full_unstemmed Reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer
title_short Reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer
title_sort reciprocal interactions between tumour cell populations enhance growth and reduce radiation sensitivity in prostate cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782740/
https://www.ncbi.nlm.nih.gov/pubmed/33398023
http://dx.doi.org/10.1038/s42003-020-01529-5
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