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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...

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Autores principales: Yan, Zedong, Wang, Dan, Cai, Jing, Shen, Liangliang, Jiang, Maogang, Liu, Xiyu, Huang, Jinghui, Zhang, Yong, Luo, Erping, Jing, Da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
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.
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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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