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Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels
Tumour recurrence frequently occurs after radiotherapy, but the characteristics, intratumoural localization and post-irradiation behaviour of radioresistant cancer cells remain largely unknown. Here we develop a sophisticated strategy to track the post-irradiation fate of the cells, which exist in p...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337987/ https://www.ncbi.nlm.nih.gov/pubmed/22510688 http://dx.doi.org/10.1038/ncomms1786 |
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author | Harada, Hiroshi Inoue, Masahiro Itasaka, Satoshi Hirota, Kiichi Morinibu, Akiyo Shinomiya, Kazumi Zeng, Lihua Ou, Guangfei Zhu, Yuxi Yoshimura, Michio McKenna, W. Gillies Muschel, Ruth J. Hiraoka, Masahiro |
author_facet | Harada, Hiroshi Inoue, Masahiro Itasaka, Satoshi Hirota, Kiichi Morinibu, Akiyo Shinomiya, Kazumi Zeng, Lihua Ou, Guangfei Zhu, Yuxi Yoshimura, Michio McKenna, W. Gillies Muschel, Ruth J. Hiraoka, Masahiro |
author_sort | Harada, Hiroshi |
collection | PubMed |
description | Tumour recurrence frequently occurs after radiotherapy, but the characteristics, intratumoural localization and post-irradiation behaviour of radioresistant cancer cells remain largely unknown. Here we develop a sophisticated strategy to track the post-irradiation fate of the cells, which exist in perinecrotic regions at the time of radiation. Although the perinecrotic tumour cells are originally hypoxia-inducible factor 1 (HIF-1)-negative, they acquire HIF-1 activity after surviving radiation, which triggers their translocation towards tumour blood vessels. HIF-1 inhibitors suppress the translocation and decrease the incidence of post-irradiation tumour recurrence. For the first time, our data unveil the HIF-1-dependent cellular dynamics during post-irradiation tumour recurrence and provide a rational basis for targeting HIF-1 after radiation therapy. |
format | Online Article Text |
id | pubmed-3337987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33379872012-04-27 Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels Harada, Hiroshi Inoue, Masahiro Itasaka, Satoshi Hirota, Kiichi Morinibu, Akiyo Shinomiya, Kazumi Zeng, Lihua Ou, Guangfei Zhu, Yuxi Yoshimura, Michio McKenna, W. Gillies Muschel, Ruth J. Hiraoka, Masahiro Nat Commun Article Tumour recurrence frequently occurs after radiotherapy, but the characteristics, intratumoural localization and post-irradiation behaviour of radioresistant cancer cells remain largely unknown. Here we develop a sophisticated strategy to track the post-irradiation fate of the cells, which exist in perinecrotic regions at the time of radiation. Although the perinecrotic tumour cells are originally hypoxia-inducible factor 1 (HIF-1)-negative, they acquire HIF-1 activity after surviving radiation, which triggers their translocation towards tumour blood vessels. HIF-1 inhibitors suppress the translocation and decrease the incidence of post-irradiation tumour recurrence. For the first time, our data unveil the HIF-1-dependent cellular dynamics during post-irradiation tumour recurrence and provide a rational basis for targeting HIF-1 after radiation therapy. Nature Pub. Group 2012-04-17 /pmc/articles/PMC3337987/ /pubmed/22510688 http://dx.doi.org/10.1038/ncomms1786 Text en Copyright © 2012, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Article Harada, Hiroshi Inoue, Masahiro Itasaka, Satoshi Hirota, Kiichi Morinibu, Akiyo Shinomiya, Kazumi Zeng, Lihua Ou, Guangfei Zhu, Yuxi Yoshimura, Michio McKenna, W. Gillies Muschel, Ruth J. Hiraoka, Masahiro Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels |
title | Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels |
title_full | Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels |
title_fullStr | Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels |
title_full_unstemmed | Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels |
title_short | Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels |
title_sort | cancer cells that survive radiation therapy acquire hif-1 activity and translocate towards tumour blood vessels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337987/ https://www.ncbi.nlm.nih.gov/pubmed/22510688 http://dx.doi.org/10.1038/ncomms1786 |
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