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Celecoxib inhibits insulin-like growth factor 1 induced growth and invasion in non-small cell lung cancer

机译:塞来昔布抑制胰岛素样生长因子1诱导的非小细胞肺癌的生长和侵袭

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Despite a large number of studies indicating that celecoxib plays an important role in the prevention and treatment of tumors, the detailed molecular mechanisms are not well understood. The aim of the present study was to investigate the effect of celecoxib on insulin-like growth factor 1 (IGF-1)-induced growth and invasion in non-small cell lung cancer (NSCLC). For these experiments, IGF-1-induced cell growth and invasion were analyzed in A549 cells in the presence and absence of celecoxib. The effects of celecoxib on the expression of phosphorylated type-1 IGF receptor (IGF-1R) and phosphorylated AKT (p-AKT) were examined using western blot analysis. The influence of celecoxib on IGF-binding protein-3 (IGFBP-3) expression was analyzed using ELISA. Celecoxib inhibited IGF-1-stimulated growth and invasion in a dose-dependent manner. Celecoxib also reduced the expression of IGF-1R, IGFBP-3 and phosphorylation of AKT. The results suggest that modulating the IGF axis may be a new mechanism for the anticancer effect of celecoxib on NSCLC.
机译:尽管有大量研究表明塞来昔布在肿瘤的预防和治疗中起着重要作用,但尚未充分了解其详细的分子机制。本研究的目的是研究塞来昔布对胰岛素样生长因子1(IGF-1)诱导的非小细胞肺癌(NSCLC)生长和侵袭的影响。对于这些实验,在存在和不存在塞来昔布的情况下,在A549细胞中分析了IGF-1诱导的细胞生长和侵袭。使用蛋白质印迹分析检查了塞来昔布对磷酸化的1型IGF受体(IGF-1R)和磷酸化的AKT(p-AKT)表达的影响。使用ELISA分析了塞来昔布对IGF结合蛋白3(IGFBP-3)表达的影响。塞来昔布以剂量依赖性方式抑制IGF-1刺激的生长和侵袭。塞来昔布还降低了IGF-1R,IGFBP-3的表达和AKT的磷酸化。结果表明,调节IGF轴可能是塞来昔布对NSCLC抗癌作用的新机制。

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