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Inhibition of gastric cancer cell growth by a PI3K-mTOR dual inhibitor GSK1059615  期刊论文  

  • 编号:
    205534b8-9b71-4001-9912-e238494b2d07
  • 作者:
  • 语种:
    英文
  • 期刊:
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS ISSN:0006-291X 2019 年 511 卷 1 期 (13 - 20) ; MAR 26
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  • 摘要:

    Gastric cancer (GC) is a common malignancy. Developing novel and efficient anti-GC agents is urgent. GSK1059615 is a P13K (phosphatidylinositol 3-kinase) and mTOR (mammalian target of rapamycin) dual inhibitor. It activity in human GC cells is tested here. In AGS cells and primary human GC cells, GSK1059615 potently inhibited cell growth, survival, proliferation and cell cycle progression. Further, significant apoptosis activation was detected in GSK1059615-treated GC cells. Contrarily in the primary human gastric epithelial cells, GSK1059615 failed to induce significant cytotoxicity and apoptosis. GSK1059615 blocked PI3K-AKT-mTOR cascade activation, inducing microRNA-9 downregulation but LMX1A (LIM homeobox transcription factor 1 alpha) upregulation in GC cells. Significantly, GSK1059615 administration (i.p., daily, at 10 or 30 mg/kg) in nude mice potently inhibited subcutaneous AGS xenograft growth. AKT-mTOR inhibition and LMX1A upregulation were detected in AGS xenograft tissues with GSK1059615 administration. Together, we conclude that GSK1059615 inhibits GC cell growth in vitro and in vivo. (C) 2019 Elsevier Inc. All rights reserved.

  • 推荐引用方式
    GB/T 7714:
    Bei Songhua,Li Fan,Li Huanqin, et al. Inhibition of gastric cancer cell growth by a PI3K-mTOR dual inhibitor GSK1059615 [J].BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2019,511(1):13-20.
  • APA:
    Bei Songhua,Li Fan,Li Huanqin,Li Jian,&Feng Li.(2019).Inhibition of gastric cancer cell growth by a PI3K-mTOR dual inhibitor GSK1059615 .BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,511(1):13-20.
  • MLA:
    Bei Songhua, et al. "Inhibition of gastric cancer cell growth by a PI3K-mTOR dual inhibitor GSK1059615" .BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 511,1(2019):13-20.
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