...
首页> 外文期刊>Tumour biology : >FTY720 reduces migration and invasion of human glioblastoma cell lines via inhibiting the PI3K/AKT/mTOR/p70S6K signaling pathway.
【24h】

FTY720 reduces migration and invasion of human glioblastoma cell lines via inhibiting the PI3K/AKT/mTOR/p70S6K signaling pathway.

机译:FTY720通过抑制PI3K / AKT / mTOR / p70S6K信号通路来减少人胶质母细胞瘤细胞系的迁移和侵袭。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

2-Amino-2-[2-(4-octylphenyl)]-1,3-propanediol hydrochloride (FTY720), a synthetic compound from Isaria sinclairii, has been proven to possess various biological benefits including anti-cancer activity. However, the effects and related mechanisms of FTY720 on the migration and invasion of glioblastoma cells are still unclear. In the present study, we utilized U251MG and U87MG human glioblastoma cell lines to assess the effects of FTY720. We found that FTY720 significantly inhibited migration and invasion of glioblastoma cells. The anti-migration and invasion effects of FTY720 were associated with its down-regulation of matrix metalloproteinase-2 (MMP-2) and MMP-9 while up-regulation of tissue inhibitor of metalloproteinase-1 (TIMP-1) and TIMP-2. Furthermore, FTY720 modulated the expression of roundabouts 1 (ROBO1), Rho-associated kinase-1 (ROCK1), and epithelial-to-mesenchymal transition (EMT)-related factors. In addition, the phosphatidylinositide 3-kinases/protein kinase B/mammalian target of rapamycin/p70S6 kinase (PI3K/AKT/mTOR/p70S6K) signaling pathway participated in FTY720-mediated suppression of migration and invasion. Thus, our findings demonstrated that FTY720 reduced glioblastoma cells migration and invasion via multiple signaling pathways, suggesting that FTY720 is a potential therapeutic agent against glioblastoma.
机译:2-氨基-2- [2-(4-辛基苯基)]-1,3-丙二醇盐酸盐(FTY720)是辛苦伊萨里亚(Isaria sinclairii)的合成化合物,已被证明具有多种生物益处,包括抗癌活性。但是,FTY720对胶质母细胞瘤细胞迁移和侵袭的影响及其相关机制仍不清楚。在本研究中,我们利用U251MG和U87MG人胶质母细胞瘤细胞系来评估FTY720的作用。我们发现FTY720显着抑制胶质母细胞瘤细胞的迁移和侵袭。 FTY720的抗迁移和侵袭作用与其上调基质金属蛋白酶2(MMP-2)和MMP-9的表达有关,而上调金属蛋白酶-1(TIMP-1)和TIMP-2的组织抑制剂的作用。 。此外,FTY720调节回旋处1(ROBO1),Rho相关激酶1(ROCK1)和上皮-间充质转化(EMT)相关因子的表达。此外,磷脂酰肌醇3激酶/蛋白激酶B /雷帕霉素/ p70S6激酶的哺乳动物靶标(PI3K / AKT / mTOR / p70S6K)信号通路参与了FTY720介导的迁移和侵袭抑制。因此,我们的研究结果表明FTY720通过多种信号通路减少了胶质母细胞瘤细胞的迁移和侵袭,提示FTY720是针对胶质母细胞瘤的潜在治疗剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号