Effects of atmospheric pressure cold plasma on human hepatocarcinoma cell and its 5-fluorouracil resistant cell line

  • H. Yang
    Huazhong University of Science and Technology 1 College of Life Science and Technology, , Wuhan, Hubei 430074, People's Republic of China
  • R. Lu
    School Hospital of Huazhong University of Science and Technology 2 , Wuhan, Hubei 430074, People's Republic of China
  • Y. Xian
    Huazhong University of Science and Technology 3 State Key Laboratory of Advanced Electromagnetic Engineering and Technology, , Wuhan, Hubei 430074, People's Republic of China
  • L. Gan
    Huazhong University of Science and Technology 1 College of Life Science and Technology, , Wuhan, Hubei 430074, People's Republic of China
  • X. Lu
    Huazhong University of Science and Technology 3 State Key Laboratory of Advanced Electromagnetic Engineering and Technology, , Wuhan, Hubei 430074, People's Republic of China
  • X. Yang
    Huazhong University of Science and Technology 1 College of Life Science and Technology, , Wuhan, Hubei 430074, People's Republic of China

説明

<jats:p>Atmospheric pressure cold plasma showed selective killing efficiency on cancer cells in vitro and in vivo, which makes plasma a potential option for cancer therapy. However, the plasma effects on chemotherapeutic drugs-resistant cells are rarely to be found. In this paper, the effects of plasma on human hepatocellular carcinoma Bel7402 cells and 5-fluorouracil (5-FU) resistant Bel7402/5FU cells were intensively investigated. The results showed that plasma induced superior toxicity to Bel7402 cells compared with Bel7402/5FU cells. Incubation with plasma-treated medium for 20 s induced more than 85% death rate in Bel7402 cells, while the same death ratio was achieved when Bel7402/5FU cells were treated for as long as 300 s. The hydrogen peroxide in the medium played a leading role in the cytotoxicity effects. Further studies implicated that when the treatment time was shorter than 60 s, the depolarization of mitochondrial membrane potential and apoptosis occurred through the intracellular reactive oxygen species accumulation in Bel7402 cells. Molecular analysis showed an increase in the transcription factor activity for AP-1, NF-кB, and p53 in Bel7402 cells. No obvious damage could be detected in plasma-treated Bel7402/5FU cells due to the strong intracellular reactive oxygen stress scavenger system.</jats:p>

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