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High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field
Radiotherapy increases tumor cure and survival rates; however, radiotherapy-induced bone damage remains a common issue for which effective countermeasures are lacking, especially considering tumor recurrence risks. We report a high-specificity protection technique based on noninvasive electromagneti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401628/ https://www.ncbi.nlm.nih.gov/pubmed/36001662 http://dx.doi.org/10.1126/sciadv.abq0222 |
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author | Yan, Zedong Wang, Dan Cai, Jing Shen, Liangliang Jiang, Maogang Liu, Xiyu Huang, Jinghui Zhang, Yong Luo, Erping Jing, Da |
author_facet | Yan, Zedong Wang, Dan Cai, Jing Shen, Liangliang Jiang, Maogang Liu, Xiyu Huang, Jinghui Zhang, Yong Luo, Erping Jing, Da |
author_sort | Yan, Zedong |
collection | PubMed |
description | Radiotherapy increases tumor cure and survival rates; however, radiotherapy-induced bone damage remains a common issue for which effective countermeasures are lacking, especially considering tumor recurrence risks. We report a high-specificity protection technique based on noninvasive electromagnetic field (EMF). A unique pulsed-burst EMF (PEMF) at 15 Hz and 2 mT induces notable Ca(2+) oscillations with robust Ca(2+) spikes in osteoblasts in contrast to other waveforms. This waveform parameter substantially inhibits radiotherapy-induced bone loss by specifically modulating osteoblasts without affecting other bone cell types or tumor cells. Mechanistically, primary cilia are identified as major PEMF sensors in osteoblasts, and the differentiated ciliary expression dominates distinct PEMF sensitivity between osteoblasts and tumor cells. PEMF-induced unique Ca(2+) oscillations depend on interactions between ciliary polycystins-1/2 and endoplasmic reticulum, which activates the Ras/MAPK/AP-1 axis and subsequent DNA repair Ku70 transcription. Our study introduces a previously unidentified method against radiation-induced bone damage in a noninvasive, cost-effective, and highly specific manner. |
format | Online Article Text |
id | pubmed-9401628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-94016282022-08-26 High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field Yan, Zedong Wang, Dan Cai, Jing Shen, Liangliang Jiang, Maogang Liu, Xiyu Huang, Jinghui Zhang, Yong Luo, Erping Jing, Da Sci Adv Biomedicine and Life Sciences Radiotherapy increases tumor cure and survival rates; however, radiotherapy-induced bone damage remains a common issue for which effective countermeasures are lacking, especially considering tumor recurrence risks. We report a high-specificity protection technique based on noninvasive electromagnetic field (EMF). A unique pulsed-burst EMF (PEMF) at 15 Hz and 2 mT induces notable Ca(2+) oscillations with robust Ca(2+) spikes in osteoblasts in contrast to other waveforms. This waveform parameter substantially inhibits radiotherapy-induced bone loss by specifically modulating osteoblasts without affecting other bone cell types or tumor cells. Mechanistically, primary cilia are identified as major PEMF sensors in osteoblasts, and the differentiated ciliary expression dominates distinct PEMF sensitivity between osteoblasts and tumor cells. PEMF-induced unique Ca(2+) oscillations depend on interactions between ciliary polycystins-1/2 and endoplasmic reticulum, which activates the Ras/MAPK/AP-1 axis and subsequent DNA repair Ku70 transcription. Our study introduces a previously unidentified method against radiation-induced bone damage in a noninvasive, cost-effective, and highly specific manner. American Association for the Advancement of Science 2022-08-24 /pmc/articles/PMC9401628/ /pubmed/36001662 http://dx.doi.org/10.1126/sciadv.abq0222 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Yan, Zedong Wang, Dan Cai, Jing Shen, Liangliang Jiang, Maogang Liu, Xiyu Huang, Jinghui Zhang, Yong Luo, Erping Jing, Da High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field |
title | High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field |
title_full | High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field |
title_fullStr | High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field |
title_full_unstemmed | High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field |
title_short | High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field |
title_sort | high-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401628/ https://www.ncbi.nlm.nih.gov/pubmed/36001662 http://dx.doi.org/10.1126/sciadv.abq0222 |
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