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Nonthermal Plasma Induces Apoptosis in ATC Cells: Involvement of JNK and p38 MAPK-Dependent ROS

Authors
Lee, Sei YoungKang, Sung UnKim, Kang IlKang, SamShin, Yoo SeobChang, Jae WonYang, Sang SikLee, KeunhoLee, Jong-SooMoon, EunpyoKim, Chul-Ho
Issue Date
Nov-2014
Publisher
YONSEI UNIV COLL MEDICINE
Keywords
Nonthermal plasma; ROS; anaplastic thyroid cancer; apoptosis; helium; oxygen
Citation
YONSEI MEDICAL JOURNAL, v.55, no.6, pp 1640 - 1647
Pages
8
Journal Title
YONSEI MEDICAL JOURNAL
Volume
55
Number
6
Start Page
1640
End Page
1647
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/11613
DOI
10.3349/ymj.2014.55.6.1640
ISSN
0513-5796
1976-2437
Abstract
Purpose: To determine the effects of nonthermal plasma (NTP) induced by helium (He) alone or He plus oxygen (O-2) on the generation of reactive oxygen species (ROS) and cell death in anaplastic thyroid cancer cells. Materials and Methods: NTP was generated in He alone or He plus O-2 blowing through a nozzle by applying a high alternating current voltage to the discharge electrodes. Optical emission spectroscopy was used to identify various excited plasma species. The apoptotic effect of NTP on the anaplastic thyroid cancer cell lines, such as HTH83, U-HTH 7, and SW1763, was verified with annexin V/propidium staining and TUNEL assay. ROS formation after NTP treatment was identified with fluorescence-activated cell sorting with DCFDA staining. The mitogen-activated protein kinase pathways and caspase cascade were investigated to evaluate the molecular mechanism involved and cellular targets of plasma. Results: NTP induced significant apoptosis in all three cancer cell lines. The plasma using He and O-2 generated more O-2-related species, and increased apoptosis and intracellular ROS formation compared with the plasma using He alone. NTP treatment of SW1763 increased the expression of phosphor-JNK, phosphor-p38, and caspase-3, but not phosphor-ERK. Apoptosis of SW1763 as well as expressions of elevated phosphor-JNK, phosphor-p38, and caspase-3 induced by NTP were effectively inhibited by intracellular ROS scavengers. Conclusion: NT? using He plus O-2 induced significant apoptosis in anaplastic cancer cell lines through intracellular ROS formation. This may represent a new promising treatment modality for this highly lethal disease.
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