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Immunobiology of cancer-associated fibroblasts in the context of radiotherapy

Radiotherapy (RT) still represents a mainstay of treatment in clinical oncology. Traditionally, the effectiveness of radiotherapy has been attributed to the killing potential of ionizing radiation (IR) over malignant cells, however, it has become clear that therapeutic efficacy of RT also involves a...

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Autores principales: Hellevik, Turid, Berzaghi, Rodrigo, Lode, Kristin, Islam, Ashraful, Martinez-Zubiaurre, Inigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524905/
https://www.ncbi.nlm.nih.gov/pubmed/34663337
http://dx.doi.org/10.1186/s12967-021-03112-w
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author Hellevik, Turid
Berzaghi, Rodrigo
Lode, Kristin
Islam, Ashraful
Martinez-Zubiaurre, Inigo
author_facet Hellevik, Turid
Berzaghi, Rodrigo
Lode, Kristin
Islam, Ashraful
Martinez-Zubiaurre, Inigo
author_sort Hellevik, Turid
collection PubMed
description Radiotherapy (RT) still represents a mainstay of treatment in clinical oncology. Traditionally, the effectiveness of radiotherapy has been attributed to the killing potential of ionizing radiation (IR) over malignant cells, however, it has become clear that therapeutic efficacy of RT also involves activation of innate and adaptive anti-tumor immune responses. Therapeutic irradiation of the tumor microenvironment (TME) provokes profound cellular and biological reconfigurations which ultimately may influence immune recognition. As one of the major constituents of the TME, cancer-associated fibroblasts (CAFs) play central roles in cancer development at all stages and are recognized contributors of tumor immune evasion. While some studies argue that RT affects CAFs negatively through growth arrest and impaired motility, others claim that exposure of fibroblasts to RT promotes their conversion into a more activated phenotype. Nevertheless, despite the well-described immunoregulatory functions assigned to CAFs, little is known about the interplay between CAFs and immune cells in the context of RT. In this review, we go over current literature on the effects of radiation on CAFs and the influence that CAFs have on radiotherapy outcomes, and we summarize present knowledge on the transformed cellular crosstalk between CAFs and immune cells after radiation.
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spelling pubmed-85249052021-10-22 Immunobiology of cancer-associated fibroblasts in the context of radiotherapy Hellevik, Turid Berzaghi, Rodrigo Lode, Kristin Islam, Ashraful Martinez-Zubiaurre, Inigo J Transl Med Review Radiotherapy (RT) still represents a mainstay of treatment in clinical oncology. Traditionally, the effectiveness of radiotherapy has been attributed to the killing potential of ionizing radiation (IR) over malignant cells, however, it has become clear that therapeutic efficacy of RT also involves activation of innate and adaptive anti-tumor immune responses. Therapeutic irradiation of the tumor microenvironment (TME) provokes profound cellular and biological reconfigurations which ultimately may influence immune recognition. As one of the major constituents of the TME, cancer-associated fibroblasts (CAFs) play central roles in cancer development at all stages and are recognized contributors of tumor immune evasion. While some studies argue that RT affects CAFs negatively through growth arrest and impaired motility, others claim that exposure of fibroblasts to RT promotes their conversion into a more activated phenotype. Nevertheless, despite the well-described immunoregulatory functions assigned to CAFs, little is known about the interplay between CAFs and immune cells in the context of RT. In this review, we go over current literature on the effects of radiation on CAFs and the influence that CAFs have on radiotherapy outcomes, and we summarize present knowledge on the transformed cellular crosstalk between CAFs and immune cells after radiation. BioMed Central 2021-10-18 /pmc/articles/PMC8524905/ /pubmed/34663337 http://dx.doi.org/10.1186/s12967-021-03112-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Review
Hellevik, Turid
Berzaghi, Rodrigo
Lode, Kristin
Islam, Ashraful
Martinez-Zubiaurre, Inigo
Immunobiology of cancer-associated fibroblasts in the context of radiotherapy
title Immunobiology of cancer-associated fibroblasts in the context of radiotherapy
title_full Immunobiology of cancer-associated fibroblasts in the context of radiotherapy
title_fullStr Immunobiology of cancer-associated fibroblasts in the context of radiotherapy
title_full_unstemmed Immunobiology of cancer-associated fibroblasts in the context of radiotherapy
title_short Immunobiology of cancer-associated fibroblasts in the context of radiotherapy
title_sort immunobiology of cancer-associated fibroblasts in the context of radiotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524905/
https://www.ncbi.nlm.nih.gov/pubmed/34663337
http://dx.doi.org/10.1186/s12967-021-03112-w
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