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Mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity
Radiotherapy is among the routine treatment options for malignant tumors. And it damages DNA and other cellular organelles in target cells by using ionizing radiation produced by various rays, killing the cells. In recent years, multiple studies have demonstrated that exosomes are mechanistically in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052527/ https://www.ncbi.nlm.nih.gov/pubmed/35484557 http://dx.doi.org/10.1186/s12967-022-03392-w |
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author | Sun, Huihui Sun, Rui Song, Xing Gu, Wendong Shao, Yingjie |
author_facet | Sun, Huihui Sun, Rui Song, Xing Gu, Wendong Shao, Yingjie |
author_sort | Sun, Huihui |
collection | PubMed |
description | Radiotherapy is among the routine treatment options for malignant tumors. And it damages DNA and other cellular organelles in target cells by using ionizing radiation produced by various rays, killing the cells. In recent years, multiple studies have demonstrated that exosomes are mechanistically involved in regulating tumor formation, development, invasion and metastasis, and immune evasion. The latest research shows that radiation can affect the abundance and composition of exosomes as well as cell-to-cell communication. In the environment, exosome-carried miRNAs, circRNA, mRNA, and proteins are differentially expressed in cancer cells, while these molecules play a role in numerous biological processes, including the regulation of oncogene expression, mediation of signaling pathways in cancer cells, remodeling of tumor-related fibroblasts, regulation of cell radiosensitivity, and so forth. Therefore, elucidation of the mechanism underlying the role of exosomes in radiotherapy of malignant tumors is crucial for improving the efficacy of radiotherapy. This review will summarize the research advances in radiosensitivity of malignant tumors related to exosomes. |
format | Online Article Text |
id | pubmed-9052527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90525272022-04-30 Mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity Sun, Huihui Sun, Rui Song, Xing Gu, Wendong Shao, Yingjie J Transl Med Review Radiotherapy is among the routine treatment options for malignant tumors. And it damages DNA and other cellular organelles in target cells by using ionizing radiation produced by various rays, killing the cells. In recent years, multiple studies have demonstrated that exosomes are mechanistically involved in regulating tumor formation, development, invasion and metastasis, and immune evasion. The latest research shows that radiation can affect the abundance and composition of exosomes as well as cell-to-cell communication. In the environment, exosome-carried miRNAs, circRNA, mRNA, and proteins are differentially expressed in cancer cells, while these molecules play a role in numerous biological processes, including the regulation of oncogene expression, mediation of signaling pathways in cancer cells, remodeling of tumor-related fibroblasts, regulation of cell radiosensitivity, and so forth. Therefore, elucidation of the mechanism underlying the role of exosomes in radiotherapy of malignant tumors is crucial for improving the efficacy of radiotherapy. This review will summarize the research advances in radiosensitivity of malignant tumors related to exosomes. BioMed Central 2022-04-28 /pmc/articles/PMC9052527/ /pubmed/35484557 http://dx.doi.org/10.1186/s12967-022-03392-w Text en © The Author(s) 2022 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 Sun, Huihui Sun, Rui Song, Xing Gu, Wendong Shao, Yingjie Mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity |
title | Mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity |
title_full | Mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity |
title_fullStr | Mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity |
title_full_unstemmed | Mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity |
title_short | Mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity |
title_sort | mechanism and clinical value of exosomes and exosomal contents in regulating solid tumor radiosensitivity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052527/ https://www.ncbi.nlm.nih.gov/pubmed/35484557 http://dx.doi.org/10.1186/s12967-022-03392-w |
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