Electromagnetic fields alter the motility of metastatic breast cancer cells.

Author: Garg AA1, Jones TH1, Moss SM2, Mishra S3,4, Kaul K3,4, Ahirwar DK3,4, Ferree J1, Kumar P1, Subramaniam D5, Ganju RK3,4, Subramaniam VV6,7, Song JW8,9
Affiliation:
1Department of Mechanical and Aerospace Engineering, The Ohio State University, Columbus, OH, 43210, USA.
2Department of Biomedical Engineering, The Ohio State University, Columbus, OH, 43210, USA.
3Department of Pathology, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
4Comprehensive Cancer Center, The Ohio State University, Columbus, OH, 43210, USA.
5College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
6Department of Mechanical and Aerospace Engineering, The Ohio State University, Columbus, OH, 43210, USA. subramaniam.1@osu.edu.
7Comprehensive Cancer Center, The Ohio State University, Columbus, OH, 43210, USA. subramaniam.1@osu.edu.
8Department of Mechanical and Aerospace Engineering, The Ohio State University, Columbus, OH, 43210, USA. song.1069@osu.edu.
9Comprehensive Cancer Center, The Ohio State University, Columbus, OH, 43210, USA. song.1069@osu.edu.
Conference/Journal: Commun Biol.
Date published: 2019 Aug 8
Other: Volume ID: 2 , Issue ID: 1 , Pages: 303 , Special Notes: doi: 10.1038/s42003-019-0550-z. , Word Count: 154


Interactions between cells and their environment influence key physiologic processes such as their propensity to migrate. However, directed migration controlled by extrinsically applied electrical signals is poorly understood. Using a novel microfluidic platform, we found that metastatic breast cancer cells sense and respond to the net direction of weak (∼100 µV cm-1), asymmetric, non-contact induced Electric Fields (iEFs). iEFs inhibited EGFR (Epidermal Growth Factor Receptor) activation, prevented formation of actin-rich filopodia, and hindered the motility of EGF-treated breast cancer cells. The directional effects of iEFs were nullified by inhibition of Akt phosphorylation. Moreover, iEFs in combination with Akt inhibitor reduced EGF-promoted motility below the level of untreated controls. These results represent a step towards isolating the coupling mechanism between cell motility and iEFs, provide valuable insights into how iEFs target multiple diverging cancer cell signaling mechanisms, and demonstrate that electrical signals are a fundamental regulator of cancer cell migration.

PMID: 31925108 DOI: 10.1038/s42003-019-0550-z

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