
what are Tumor Treating Fields (TTFields)?
Tumor Treating Fields (TTFields) are electric fields that exert physical forces to kill cancer cells via multiple, distinct mechanisms.1-7
- Electric fields have different effects on the human body depending on their frequency. 1,8-10
- Because cancer cells contain electrically charged components, they can be influenced by electric fields.7
how does TTFields Therapy work?
TTFields therapy has multiple, distinct mechanisms of action that work together to selectively target and kill cancer cells.1-5
TTFields do not significantly affect healthy cells because healthy cells have different properties (including division rate, morphology, and electrical properties) than cancer cells.


disruption of mitosis
In preclinical models, TTFields have been shown to disrupt mitosis in cancer cells by exerting electric forces on their polar components (e.g., microtubule spindle formation during mitosis), disrupting their normal localization (place in cell membrane) and function, ultimately leading to cell death.1-3

in metaphase
TTFields impair microtubule assembly in cancer cells, leading to aberrant mitotic spindle formation.2,4

in anaphase
TTFields disrupt the arrangement of septin at the anaphase cleavage furrow in cancer cells, inducing cytoplasmic membrane blebbing, mitotic failure, and asymmetric chromosome segregation.1,5

in telophase
TTFields push polar organelles and macromolecules (a process called dielectrophoresis) to the bridge between the forming daughter cells, where - due to the hourglass shape - TTFields intensity is highest.4,5
interference with cell movement and migration
In preclinical models, TTFields have been shown to alter the organization and dynamics of the cytoskeleton, disrupting cancer cell motility and migration, which are essential for metastasis.1
TTFields disrupt the direction and diminish the abundance of the microtubule network, interfering with cancer cell migration.1


enhancement of antitumor immunity
In pre-clinical models, TTFields-mediated cell disruption has been shown to activate the immune system and induce a downstream immunogenic anti-tumor response.1,12-16
downregulation of DNA damage response
In preclinical models, TTFields have been shown to downregulate important DNA damage response.1,17-20

TTFields therapy works with other cancer treatments in approved indications
Due to its multimechanistic actions, TTFields therapy can be added to cancer treatment modalities in approved indications and demonstrates enhanced effects across solid tumor types when used with chemotherapy, radiotherapy, immune checkpoint inhibition, or targeted therapies in preclinical models. TTFields therapy provides clinical versatility that has the potential to help address treatment challenges across a range of solid tumors.
GLB-CC-00328. Nov 2025
References: 1. Karanam NK, Story MD. An overview of potential novel mechanisms of action underlying tumor treating fields-induced cancer cell death and their clinical implications. Int J Radiat Biol. 2021;97(8):1044-1054. doi:10.1080/09553002.2020.1837984 2. Voloshin T, Schneiderman RS, Volodin A, et al. Tumor treating fields (TTFields) hinder cancer cell motility through regulation of microtubule and actin dynamics. Cancers (Basel). 2020;12(10):1-18. doi:10.3390/cancers12103016 3. Mun EJ, Babiker HM, Weinberg U, Kirson ED, Von Hoff DD. Tumor-treating fields: a fourth modality in cancer treatment. Clin Cancer Res. 2018;24(2):266-275. doi:10.1158/1078-0432.CCR-17-1117 4. Cooper GM. The development and causes of cancer. In: The Cell: A Molecular Approach. 2nd ed. Sinauer Associates; 2000:chap 15. Accessed June 21, 2022. https://www.ncbi.nlm.nih.gov/books/NBK9963/ 5. Baba AI, Câtoi C. Tumor cell morphology. In: Comparative Oncology. The Publishing House of the Romanian Academy; 2007:chap 3. Accessed June 21, 2022. https://www.ncbi.nlm.nih.gov/books/NBK9553/ 6. Giladi M, Schneiderman RS, Voloshin T, et al. Mitotic spindle disruption by alternating electric fields leads to improper chromosome segregation and mitotic catastrophe in cancer cells. Sci Rep. 2015;5:1-16. doi:10.1038/srep18046 7. Kirson ED, Dbalý V, Tovaryš F, et al. Alternating electric fields arrest cell proliferation in animal tumor models and human brain tumors. Proc Natl Acad Sci U S A. 2007;104(24):10152-10157. doi:10.1073/pnas.0702916104 8. Ablation for liver cancer. American Cancer Society. Updated April 1, 2019. Accessed June 21, 2022. https://www.cancer.org/cancer/liver-cancer/treating/tumor-ablation.html 9. Krauss JK, Lipsman N, Aziz T, et al. Technology of deep brain stimulation: current status and future directions. Nat Rev Neurol. 2021;17(2):75-87. doi:10.1038/s41582-020-00426-z 10. Mulpuru SK, Madhavan M, McLeod CJ, Cha Y-M, Friedman PA. Cardiac pacemakers: function, troubleshooting, and management. Am Coll Cardiol. 2017;69(2):189-210. doi:10.1016/j.jacc.2016.10.061 11. Wenger C, Giladi M, Bomzon Z, Salvador R, Basser PJ, Miranda PC. Modeling Tumor Treating Fields (TTFields) application in single cells during metaphase and telophase. Annu Int Conf IEEE Eng Med Biol Soc. 2015;2015:6892-6895. doi:10.1109/EMBC.2015.7319977 12. Voloshin T, Kaynan N, Davidi S, Porat Y, Shteingauz A, Schneiderman RS, Zeevi E, Munster M, Blat R, Tempel Brami C, Cahal S, Itzhaki A, et al. Tumor-treating fields (TTFields) induce immunogenic cell death resulting in enhanced antitumor efficacy when combined with anti-PD-1 therapy. Cancer Immunol Immunother 2020;69: 1191-204. 13. Barsheshet Y, Voloshin T, Brant B, Cohen G, Koren L, Blatt R, Cahal S, Haj Khalil T, Zemer Tov E, Paz R, Klein-Goldberg A, Tempel-Brami C, et al. Tumor Treating Fields (TTFields) Concomitant with Immune Checkpoint Inhibitors Are Therapeutically Effective in Non-Small Cell Lung Cancer (NSCLC) In Vivo Model. Int J Mol Sci 2022;23. 14. Lin W, Wang Y, Li M, Feng J, Yue Y, Yu J, Hu Y, Suo Y. Tumor treating fields enhance anti-PD therapy by improving CCL2/8 and CXCL9/CXCL10 expression through inducing immunogenic cell death in NSCLC models. BMC Cancer 2025;25: 489. 15. Chen D, Le SB, Hutchinson TE, Calinescu AA, Sebastian M, Jin D, Liu T, Ghiaseddin A, Rahman M, Tran DD. Tumor Treating Fields dually activate STING and AIM2 inflammasomes to induce adjuvant immunity in glioblastoma. J Clin Invest 2022;132. 16. Mylod C, Jenkins, Malliaras, and Gardiner. Tumor-treating fields increase cytotoxic degranulation of natural killer cells against cancer cells. Cell Reports Physical Science 2024;5: 102119. 17. Giladi M, Munster M, Schneiderman RS, et al. Tumor treating fields (TTFields) delay DNA damage repair following radiation treatment of glioma cells. Radiat Oncol. 2017;12:206. doi:10.1186/s13014-017-0941-6. 18. Karanam NK, Srinivasan K, Ding L, et al. Tumor-treating fields elicit a conditional vulnerability to ionizing radiation via the downregulation of BRCA1 signaling and reduced DNA double-strand break repair capacity in non-small cell lung cancer cell linesCell Death & Disease. 2017;8:e2711. 19. Vanderlinden A, Jones CG, Myers KN, et al. DNA damage response inhibitors enhance tumour treating fields (TTFields) potency in glioma stem-like cells. Br J Cancer. 2023;129:1829–1840. 20. Wainer-Katsir K, Haber A, Fishman H, Ding L, Story MD, Du R, Kahlert UD, Mannarino L, Mirimao F, Lupi M, D'Incalci M, Lavy-Shahaf G, et al. The transcriptomic fingerprint of cancer response to Tumor Treating Fields (TTFields). Cell Death Discov 2025;11: 319.