Document Type
Article
Publication Date
2018
Publication Title
Oncotarget
Volume
9
Issue
26
Pages
18002-18017
DOI
10.18632/oncotarget.24649
Abstract
Multiple myeloma (MM) is a fatal and incurable hematological malignancy thus new therapy need to be developed. Cold atmospheric plasma, a new technology that could generate various active species, could efficiently induce various tumor cells apoptosis. More details about the interaction of plasma and tumor cells need to be addressed before the application of gas plasma in clinical cancer treatment. In this study, we demonstrate that He+O2 plasma could efficiently induce myeloma cell apoptosis through the activation of CD95 and downstream caspase cascades. Extracellular and intracellular reactive oxygen species (ROS) accumulation is essential for CD95-mediated cell apoptosis in response to plasma treatment. Furthermore, p53 is shown to be a key transcription factor in activating CD95 and caspase cascades. More importantly, we demonstrate that CD95 expression is higher in tumor cells than in normal cells in both MM cell lines and MM clinical samples, which suggests that CD95 could be a favorable target for plasma treatment as it could selectively inactivate myeloma tumor cells. Our results illustrate the molecular details of plasma induced myeloma cell apoptosis and it shows that gas plasma could be a potential tool for myeloma therapy in the future.
Original Publication Citation
Xu, D., Xu, Y., Cui, Q., Liu, D., Liu, Z., Wang, X., . . . Kong, M. G. (2018). Cold atmospheric plasma as a potential tool for multiple myeloma treatment. Oncotarget, 9(26), 18002-18017. doi:10.18632/oncotarget.24649
Repository Citation
Xu, Dehui; Xu, Yujing; Cui, Qingjie; Liu, Dingxin; Liu, Zhijie; Wang, Xiaohua; Yang, Yanjie; Feng, Niaojuan; Liang, Rong; Chen, Hailan; Ye, Kai; and Kong, Michael G., "Cold Atmospheric Plasma as a Potential Tool for Multiple Myeloma Treatment" (2018). Bioelectrics Publications. 188.
https://digitalcommons.odu.edu/bioelectrics_pubs/188
Included in
Cancer Biology Commons, Cell Biology Commons, Medical Biotechnology Commons, Molecular Biology Commons, Oncology Commons
Comments
This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Copyright: Xu et al.