Down-regulation of Glutathione Peroxidase 4 in Oral Cancer Inhibits Tumor Growth Through SREBP1 Signaling

被引:36
作者
Fukuda, Masakatsu [1 ]
Ogasawara, Yudai [1 ]
Hayashi, Hiroyasu [1 ]
Okuyama, Ayako [1 ]
Shiono, Junya [1 ]
Inoue, Katsuyuki [1 ]
Sakashita, Hideaki [1 ]
机构
[1] Meikai Univ, Sch Dent, Div Oral & Maxillofacial Surg, Dept Diagnost & Therapeut Sci, 1-1 Keyakidai, Sakado, Saitama 3500283, Japan
关键词
Glutathione peroxidase 4; ferroptosis; SREBP; p53; human oral squamous cell carcinoma;
D O I
10.21873/anticanres.14944
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: This study aimed to elucidate the role of glutathione peroxidase 4 (GPX4) on the sterol regulatory element binding proteins (SREBPs)-proliferation pathway in oral cancer cells, and determine its protein expression in oral cancer tissues. Materials and Methods: Quantitative RT-PCR and immunoblot analysis were carried out. Cell viability assay, apoptosis detection assay, immunohistochemistry and GPX4 knockdown were performed. Results: The levels of both GPX4 mRNA and protein were highest in SAS cells. GPX4 knockdown in SAS cells, a human oral squamous cell carcinoma cell line, using GPX4 siRNA resulted in a reduction in cell number, which appeared to be due to non-apoptotic cell death such as ferroptosis. Furthermore, SREBP was clearly down-regulated by GPX4 knockdown in SAS cells. Immunopositivity for GPX4 was revealed on the membrane of human oral squamous cell carcinoma cells, and this was correlated with p53 immunoreactivity. Conclusion: GPX4 appears to play an important role in oral cancer proliferation.
引用
收藏
页码:1785 / 1792
页数:8
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