Knockdown of PSF1 expression inhibits cell proliferation in lung cancer cells in vitro
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  • 作者:Jingyao Zhang (1)
    Qifei Wu (2)
    Zhe Wang (2)
    Yong Zhang (2)
    Guangjian Zhang (2)
    Junke Fu (2)
    Chang Liu (1)

    1. Department of Hepatobiliary Surgery
    ; the First Affiliated Hospital ; Medical School ; Xi鈥檃n Jiaotong University ; Xi鈥檃n ; China
    2. Department of Thoracic Surgery
    ; the First Affiliated Hospital ; Medical School ; Xi鈥檃n Jiaotong University ; Yan Ta West Road No. 277 ; Xi鈥檃n ; Shaanxi ; 710061 ; China
  • 关键词:Cell cycle ; PSF1 ; Lung cancer ; Proliferation
  • 刊名:Tumor Biology
  • 出版年:2015
  • 出版时间:March 2015
  • 年:2015
  • 卷:36
  • 期:3
  • 页码:2163-2168
  • 全文大小:1,718 KB
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  • 刊物主题:Cancer Research;
  • 出版者:Springer Netherlands
  • ISSN:1423-0380
文摘
Partner of sld five 1 (PSF1) is a member of the heterotetrameric complex termed GINS. Previous studies have shown that PSF1 is unregulated in several cancer and associated with tumor malignant characters. However, the effects of PSF1 in lung cancer are still unclear. The goal of this study was to investigate the effects of PSF1 on the proliferation capacities of lung cancer. To start with, expression of PSF1 in 22 human lung cancer samples and adjacent non-tumor samples were detected by real-time RT-PCR and Western blotting. Our results showed that PSF1 was overexpressed in lung cancer samples compared to adjacent non-tumor samples. To achieve better insights of PSF1 functions in lung cancer cells, we used PSF1-specific small interfering RNA (siRNA) successfully inhibit the expression of PSF1 in messenger RNA (mRNA) and protein levels. In addition, we used lung cancer cell lines with different p53 gene background (p53 null and p53 wild-type). The results showed that knockdown of PSF1 inhibited cell proliferation and caused cell cycle arrest of lung cancer cells in a p53-independent manner. Our data indicated that PSF1 is functionally involved in lung cancer cell proliferation and is a potential target for lung cancer therapy.

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