Abstract

F-actin (filamentous actin) has been shown to be sensitive to mechanical stimuli and play critical roles in cell attachment, migration, and cancer metastasis, but there are very limited ways to perturb F-actin dynamics with low cell toxicity. Magnetic field is a noninvasive and reversible physical tool that can easily penetrate cells and human bodies. Here, we show that 0.1/0.4-T 4.2-Hz moderate-intensity low-frequency rotating magnetic field-induced electric field could directly decrease F-actin formation in vitro and in vivo, which results in decreased breast cancer cell migration, invasion, and attachment. Moreover, low-frequency rotating magnetic fields generated significantly different effects on F-actin in breast cancer vs. noncancerous cells, including F-actin number and their recovery after magnetic field retrieval. Using an intermittent treatment modality, low-frequency rotating magnetic fields could significantly reduce mouse breast cancer metastasis, prolong mouse survival by 31.5 to 46.0% (P < 0.0001), and improve their overall physical condition. Therefore, our work demonstrates that low-frequency rotating magnetic fields not only can be used as a research tool to perturb F-actin but also can inhibit breast cancer metastasis through F-actin modulation while having minimum effects on normal cells, which reveals their potential to be developed as temporal-controlled, noninvasive, and high-penetration physical treatments for metastatic cancer.

Details

Title
Intermittent F-actin Perturbations by Magnetic Fields Inhibit Breast Cancer Metastasis
Author
Ji, Xinmiao  VIAFID ORCID Logo  ; Tian, Xiaofei  VIAFID ORCID Logo  ; Feng, Shuang  VIAFID ORCID Logo  ; Zhang, Lei  VIAFID ORCID Logo  ; Wang, Junjun  VIAFID ORCID Logo  ; Guo, Ruowen  VIAFID ORCID Logo  ; Zhu, Yiming  VIAFID ORCID Logo  ; Yu, Xin  VIAFID ORCID Logo  ; Zhang, Yongsen; Du, Haifeng; Zablotskii, Vitalii  VIAFID ORCID Logo  ; Zhang, Xin  VIAFID ORCID Logo 
Pages
0080-0080
Publication year
2023
Publication date
2023
ISSN
20965168
e-ISSN
26395274
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3254940424
Copyright
© 2023. This work is published under (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.