The Influence of Cold Atmospheric Pressure Plasma-Treated Media on the Cell Viability, Motility, and Induction of Apoptosis in Human Non-Metastatic (MCF7) and Metastatic (MDA-MB-231) Breast Cancer Cell Lines

• Published in: International journal of molecular sciences Vol. 22; no. 8; p. 3855
• Main Authors: Terefinko, Dominik, Dzimitrowicz, Anna, Bielawska-Pohl, Aleksandra, Klimczak, Aleksandra, Pohl, Pawel, Jamroz, Piotr
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 08.04.2021; MDPI
• Subjects: Apoptosis; Atmospheric pressure; biological activity; Breast cancer; Cancer therapies; Cell culture; Cell death; Cell viability; Fever; Hyperthermia; Metastases; Metastasis; Nanoparticles; Nitrates; non-thermal plasma; Oxidative stress; Qualitative analysis; reactive oxygen and nitrogen species; Tumor cell lines; Wound healing; breast cancer; biological activity; reactive oxygen and nitrogen species; non-thermal plasma
• DOI: 10.3390/ijms22083855
• ISSN: 1422-0067; 1661-6596

Breast cancer remains the most common type of cancer, occurring in middle-aged women, and often leads to patients' death. In this work, we applied a cold atmospheric pressure plasma (CAPP)-based reaction-discharge system, one that is unique in its class, for the production of CAPP-activated media (DMEM and Opti-MEM); it is intended for further uses in breast cancer treatment. To reach this aim, different volumes of DMEM or Opti-MEM were treated by CAPP. Prepared media were exposed to the CAPP treatment at seven different time intervals and examined in respect of their impact on cell viability and motility, and the induction of the apoptosis in human non-metastatic (MCF7) and metastatic (MDA-MB-231) breast cancer cell lines. As a control, the influence of CAPP-activated media on the viability and motility, and the type of the cell death of the non-cancerous human normal MCF10A cell line, was estimated. Additionally, qualitative and quantitative analyses of the reactive oxygen and nitrogen species (RONS), generated during the CAPP operation in contact with analyzed media, were performed. Based on the conducted research, it was found that 180 s (media activation time by CAPP) should be considered as the minimal toxic dose, which significantly decreases the cell viability and the migration of MDA-MB-231 cells, and also disturbs life processes of MCF7 cells. Finally, CAPP-activated media led to the apoptosis of analyzed cell lines, especially of the metastatic MDA-MB-231 cell line. Therefore, the application of the CAPP system may be potentially applied as a therapeutic strategy for the management of highly metastatic human breast cancer.