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Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models
The effect of radiation therapy on tumor vasculature has long been a subject of debate. Increased oxygenation and perfusion have been documented during radiation therapy. Conversely, apoptosis of endothelial cells in irradiated tumors has been proposed as a major contributor to tumor control. To exa...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442312/ https://www.ncbi.nlm.nih.gov/pubmed/35848459 http://dx.doi.org/10.15252/embr.202153221 |
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author | Kaeppler, Jakob R Chen, Jianzhou Buono, Mario Vermeer, Jenny Kannan, Pavitra Cheng, Wei‐Chen Voukantsis, Dimitrios Thompson, James M Hill, Mark A Allen, Danny Gomes, Ana Kersemans, Veerle Kinchesh, Paul Smart, Sean Buffa, Francesca Nerlov, Claus Muschel, Ruth J Markelc, Bostjan |
author_facet | Kaeppler, Jakob R Chen, Jianzhou Buono, Mario Vermeer, Jenny Kannan, Pavitra Cheng, Wei‐Chen Voukantsis, Dimitrios Thompson, James M Hill, Mark A Allen, Danny Gomes, Ana Kersemans, Veerle Kinchesh, Paul Smart, Sean Buffa, Francesca Nerlov, Claus Muschel, Ruth J Markelc, Bostjan |
author_sort | Kaeppler, Jakob R |
collection | PubMed |
description | The effect of radiation therapy on tumor vasculature has long been a subject of debate. Increased oxygenation and perfusion have been documented during radiation therapy. Conversely, apoptosis of endothelial cells in irradiated tumors has been proposed as a major contributor to tumor control. To examine these contradictions, we use multiphoton microscopy in two murine tumor models: MC38, a highly vascularized, and B16F10, a moderately vascularized model, grown in transgenic mice with tdTomato‐labeled endothelium before and after a single (15 Gy) or fractionated (5 × 3 Gy) dose of radiation. Unexpectedly, even these high doses lead to little structural change of the perfused vasculature. Conversely, non‐perfused vessels and blind ends are substantially impaired after radiation accompanied by apoptosis and reduced proliferation of their endothelium. RNAseq analysis of tumor endothelial cells confirms the modification of gene expression in apoptotic and cell cycle regulation pathways after irradiation. Therefore, we conclude that apoptosis of tumor endothelial cells after radiation does not impair vascular structure. |
format | Online Article Text |
id | pubmed-9442312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94423122022-09-09 Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models Kaeppler, Jakob R Chen, Jianzhou Buono, Mario Vermeer, Jenny Kannan, Pavitra Cheng, Wei‐Chen Voukantsis, Dimitrios Thompson, James M Hill, Mark A Allen, Danny Gomes, Ana Kersemans, Veerle Kinchesh, Paul Smart, Sean Buffa, Francesca Nerlov, Claus Muschel, Ruth J Markelc, Bostjan EMBO Rep Articles The effect of radiation therapy on tumor vasculature has long been a subject of debate. Increased oxygenation and perfusion have been documented during radiation therapy. Conversely, apoptosis of endothelial cells in irradiated tumors has been proposed as a major contributor to tumor control. To examine these contradictions, we use multiphoton microscopy in two murine tumor models: MC38, a highly vascularized, and B16F10, a moderately vascularized model, grown in transgenic mice with tdTomato‐labeled endothelium before and after a single (15 Gy) or fractionated (5 × 3 Gy) dose of radiation. Unexpectedly, even these high doses lead to little structural change of the perfused vasculature. Conversely, non‐perfused vessels and blind ends are substantially impaired after radiation accompanied by apoptosis and reduced proliferation of their endothelium. RNAseq analysis of tumor endothelial cells confirms the modification of gene expression in apoptotic and cell cycle regulation pathways after irradiation. Therefore, we conclude that apoptosis of tumor endothelial cells after radiation does not impair vascular structure. John Wiley and Sons Inc. 2022-07-18 /pmc/articles/PMC9442312/ /pubmed/35848459 http://dx.doi.org/10.15252/embr.202153221 Text en © 2022 The Authors. Published under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Kaeppler, Jakob R Chen, Jianzhou Buono, Mario Vermeer, Jenny Kannan, Pavitra Cheng, Wei‐Chen Voukantsis, Dimitrios Thompson, James M Hill, Mark A Allen, Danny Gomes, Ana Kersemans, Veerle Kinchesh, Paul Smart, Sean Buffa, Francesca Nerlov, Claus Muschel, Ruth J Markelc, Bostjan Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models |
title | Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models |
title_full | Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models |
title_fullStr | Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models |
title_full_unstemmed | Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models |
title_short | Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models |
title_sort | endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442312/ https://www.ncbi.nlm.nih.gov/pubmed/35848459 http://dx.doi.org/10.15252/embr.202153221 |
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