High-specificity protection against radiation-induced bone loss by a pulsed electromagnetic field

Author:

Yan Zedong1ORCID,Wang Dan1ORCID,Cai Jing2,Shen Liangliang3,Jiang Maogang1,Liu Xiyu1,Huang Jinghui4ORCID,Zhang Yong5,Luo Erping1,Jing Da167ORCID

Affiliation:

1. Department of Biomedical Engineering, Fourth Military Medical University, Xi’an, China.

2. College of Basic Medicine, Shaanxi University of Chinese Medicine, Xianyang, China.

3. The State Key Laboratory of Cancer Biology, Department of Biochemistry and Molecular Biology, Fourth Military Medical University, Xi’an, China.

4. Institute of Orthopaedics, Xijing Hospital, Fourth Military Medical University, Xi’an, China.

5. Department of Pulmonary and Critical Care of Medicine, Xijing Hospital, Fourth Military Medical University, Xi’an, China.

6. The Ministry of Education Key Lab of Hazard Assessment and Control in Special Operational Environment, Fourth Military Medical University, Xi’an, China.

7. Shaanxi Provincial Key Laboratory of Bioelectromagnetic Detection and Intelligent Perception, Fourth Military Medical University, Xi’an, China.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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