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首页> 外文期刊>Cell & Bioscience >Growth inhibition and apoptosis in colorectal cancer cells induced by Vitamin D-Nanoemulsion (NVD): involvement of Wnt/β-catenin and other signal transduction pathways
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Growth inhibition and apoptosis in colorectal cancer cells induced by Vitamin D-Nanoemulsion (NVD): involvement of Wnt/β-catenin and other signal transduction pathways

机译:维生素D-纳米乳剂(NVD)诱导的结直肠癌细胞生长抑制和凋亡:Wnt /β-catenin和其他信号转导途径的参与

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摘要

More than the two decades, the question of whether vitamin D has a role in cancer frequency, development, and death has been premeditated in detail. Colorectal, breast, and prostate cancers have been a scrupulous spot of center, altogether, these three malignancies report for approximately 35% of cancer cases and 20% of cancer demises in the United States, and as such are a chief public health apprehension. The aim was to evaluate antitumor activity of Vitamin D-Nanoemulsion (NVD) in colorectal cancer cell lines and HCT116 xenograft model in a comprehensive approach. Two human colorectal cancer cell lines HCT116 and HT29 (gained from College of Pharmacy, King Saud University, KSA were grown. 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazoliumbromide protocol were performed to show the impact of NVD and β-catenin inhibitor (FH535) on the viability of HCT116 and HT29 cell lines. Apoptosis/cell cycle assay was performed. Analysis was done with a FACScan (Becton–Dickinson, NJ). About 10,000 cells per sample were harvested and Histograms of DNA were analyzed with ModiFitLT software (verity Software House, ME, USA). Western blotting and RT-PCR were performed for protein and gene expression respectively in in vitro and in vivo. We found that NVD induced cytotoxicity in colorectal cells in a dose-dependent manner and time dependent approach. Further, our data validated that NVD administration of human colorectal cancer HCT116 and HT29 cells resulted in cell growth arrest, alteration in molecules regulating cell cycle operative in the G2 phase of the cell cycle and apoptosis in a dose dependent approach. Further our results concluded that NVD administration decreases expression of β-catenin gene, AKT gene and Survivin gene and protein expression in in vitro and in vivo. Our findings suggest that targeting β-catenin gene may encourage the alterations of cell cycle and cell cycle regulators. Wnt/β-catenin signaling pathway possibly takes part in the genesis and progression of colorectal cancer cells through regulating cell cycle and the expression of cell cycle regulators.
机译:在过去的二十多年中,有关维生素D是否在癌症发生频率,发展和死亡中起作用的问题已经得到了详细的思考。大肠癌,乳腺癌和前列腺癌一直是中心的中心点,在美国,这三种恶性肿瘤报告约占35%的癌症病例和20%的癌症死亡,因此也是主要的公共卫生问题。目的是全面评估维生素D-纳米乳剂(NVD)在结直肠癌细胞系和HCT116异种移植模型中的抗肿瘤活性。生长了两种人结直肠癌细胞系HCT116和HT29(获自KSA,沙特国王大学药学院),进行了3​​-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物实验,以显示NVD和β-catenin抑制剂(FH535)对HCT116和HT29细胞系活力的影响;进行了凋亡/细胞周期测定;使用FACScan(Becton–Dickinson,NJ)进行了分析;每个样品大约收获了10,000个细胞用ModiFitLT软件(verity Software House,ME,USA)分析DNA的直方图,并在体内和体外分别进行蛋白质印迹和RT-PCR检测蛋白质和基因的表达,发现NVD可诱导大肠癌细胞的细胞毒性。此外,我们的数据验证了NVD施用人结肠直肠癌HCT116和HT29细胞可导致细胞生长停滞,调节在细胞G2期起作用的细胞周期的分子的改变ll周期和细胞凋亡的剂量依赖性方法。此外,我们的结果得出结论,在体外和体内,NVD给药会降低β-catenin基因,AKT基因和Survivin基因的表达以及蛋白质的表达。我们的发现表明靶向β-catenin基因可能会促进细胞周期和细胞周期调节因子的改变。 Wnt /β-catenin信号通路可能通过调节细胞周期和细胞周期调节因子的表达参与大肠癌细胞的发生和发展。

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