首页> 外文期刊>Carcinogenesis >Pomegranate fruit extract inhibits prosurvival pathways in human A549 lung carcinoma cells and tumor growth in athymic nude mice
【24h】

Pomegranate fruit extract inhibits prosurvival pathways in human A549 lung carcinoma cells and tumor growth in athymic nude mice

机译:石榴果实提取物抑制人A549肺癌的生存途径和无胸腺裸鼠的肿瘤生长

获取原文
获取原文并翻译 | 示例
           

摘要

Developing novel mechanism-based chemopreventive approaches for lung cancer through the use of dietary substances which humans can accept has become an important goal. In the present study, employing normal human bronchial epithelial cells (NHBE) and human lung carcinoma A549 cells, we first compared the growth inhibitory effects of pomegranate fruit extract (PFE). Treatment of PFE (50–150 μg/ml) for 72 h was found to result in a decrease in the viability of A549 cells but had only minimal effects on NHBE cells as assessed by the MTT and Trypan blue assays. PFE treatment of A549 cells also resulted in dose-dependent arrest of cells in G0–G1 phase of the cell cycle (as assessed by DNA cell cycle analysis). We further found that PFE treatment also resulted in (i) induction of WAF1/p21 and KIP1/p27, (ii) decrease in the protein expressions of cyclins D1, D2 and E, and (iii) decrease in cyclin-dependent kinase (cdk) 2, cdk4 and cdk6 expression. The treatment of cells with PFE inhibited (i) phosphorylation of MAPK proteins, (ii) inhibition of PI3K, (iii) phosphorylation of Akt at Thr308, (iv) NF-κB and IKKα, (v) degradation and phosphorylation of IκBα, and (vi) Ki-67 and PCNA. We also found that PFE treatment to A549 cells resulted in inhibition of NF-κB DNA-binding activity. Oral administration of PFE (0.1 and 0.2%, wt/vol) to athymic nude mice implanted with A549 cells resulted in a significant inhibition in tumor growth. Our results provide a suggestion that PFE can be a useful chemopreventive/chemotherapeutic agent against human lung cancer.
机译:通过使用人类可以接受的饮食物质开发针对肺癌的新颖的基于机制的化学预防方法已成为一个重要目标。在本研究中,我们采用正常人支气管上皮细胞(NHBE)和人肺癌A549细胞,我们首先比较了石榴果实提取物(PFE)的生长抑制作用。通过MTT和台盼蓝试验评估,发现PFE(50–150μg/ ml)处理72小时会导致A549细胞活力降低,但对NHBE细胞的影响却很小。 PFE处理A549细胞还导致细胞周期的G 0 –G 1 期细胞剂量依赖性停滞(通过DNA细胞周期分析评估)。我们进一步发现PFE治疗还导致(i)诱导WAF1 / p21和KIP1 / p27,(ii)降低细胞周期蛋白D1,D2和E的蛋白质表达,以及(iii)降低细胞周期蛋白依赖性激酶(cdk )2,cdk4和cdk6表达式。 PFE处理细胞可抑制(i)MAPK蛋白的磷酸化,(ii)PI3K的抑制,(iii)Thr 308 处Akt的磷酸化,(iv)NF-κB和IKKα,(v )IκBα的降解和磷酸化,以及(vi)Ki-67和PC​​NA。我们还发现,对A549细胞进行PFE处理可抑制NF-κBDNA结合活性。对植入A549细胞的无胸腺裸鼠口服PFE(0.1和0.2%,wt / vol)可显着抑制肿瘤生长。我们的结果表明,PFE可以作为一种有用的化学预防剂/化学治疗剂来抗人肺癌。

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