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Hypoxia regulates reactive oxygen species levels in SHG-44 glioma cells.
Jiang, Haitao; Xie, Jiangtao; Xu, Gaofeng; Su, Yongyong; Li, Jinzheng; Zhu, Mang; Wang, Maode.
Affiliation
  • Jiang H; First Affiliated Hospital, Xi'an Jiaotong University, Xi'an 710000, Shaanxi Province, China.
  • Xie J; Xianyang Central Hospital, Xianyang 712000, Shaanxi Province, China.
  • Xu G; First Affiliated Hospital, Xi'an Jiaotong University, Xi'an 710000, Shaanxi Province, China.
  • Su Y; Xianyang Central Hospital, Xianyang 712000, Shaanxi Province, China.
  • Li J; Xianyang Central Hospital, Xianyang 712000, Shaanxi Province, China.
  • Zhu M; Xi'an Central Hospital, Xi'an 710000, Shaanxi Province, China.
  • Wang M; First Affiliated Hospital, Xi'an Jiaotong University, Xi'an 710000, Shaanxi Province, China.
Neural Regen Res ; 8(6): 554-60, 2013 Feb 25.
Article in En | MEDLINE | ID: mdl-25206699
ABSTRACT
In the present study, cultured human SHG-44 glioma cells were subjected to a hypoxic environment simulated using the CoCl2 method. Flow cytometry showed increased reactive oxygen species production in these cells. Real-time reverse transcription-PCR showed significantly increased hypoxia-inducible factor-1α mRNA expression in cells exposed to the hypoxic condition. The antioxidant N-acetylcysteine significantly inhibited reactive oxygen species production and reduced hypoxia-inducible factor-1α mRNA expression in normoxic and hypoxic groups, especially in the latter group. These findings indicate that hypoxia induces reactive oxygen species production and hypoxia-inducible factor-1α mRNA expression in human SHG-44 glioma cells, and that the antioxidant N-acetylcysteine can inhibit these changes.
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