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首页> 外文期刊>Technology in cancer research & treatment. >Knockdown of Immature Colon Carcinoma Transcript 1 Inhibits Proliferation and Promotes Apoptosis of Non–Small Cell Lung Cancer Cells
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Knockdown of Immature Colon Carcinoma Transcript 1 Inhibits Proliferation and Promotes Apoptosis of Non–Small Cell Lung Cancer Cells

机译:未成无状结肠癌转录物1的敲低抑制增殖并促进非小细胞肺癌细胞的凋亡

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Non–small cell lung cancer, as the most frequent type lung cancer, has lower survival rate of 5 years, despite improvements in surgery and chemotherapy. Previous studies showed immature colon carcinoma transcript 1 is closely related to tumorigenesis of human cancer cells. In the present study, we found immature colon carcinoma transcript 1 was overexpressed in lung cancer tissues using Oncomine database mining, and the biological effect of immature colon carcinoma transcript 1 was investigated in non–small cell lung cancer cell lines 95D and A549. Lentivirus-mediated RNA interference was used to knock down immature colon carcinoma transcript 1 expression in 95D and A549 cells in vitro, and the knockdown efficiency was determined using quantitative real-time polymerase chain reaction and Western blot assay. Knockdown of immature colon carcinoma transcript 1 significantly suppressed non–small cell lung cancer cell proliferation and colony formation ability confirmed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and colony formation assay. Flow cytometry was applied to measure cell cycle arrest, and the result showed the cell cycle arrested in G2/M phase in 95D cells and arrested in G0/G1 phase in A549 cells. Furthermore, we measured the levels of cell cycle–associated proteins by Western blot analysis and found immature colon carcinoma transcript 1–mediated cell proliferation inhibition appeared due to downregulation of cell cycle activator cyclin D1 and upregulation of cell cycle inhibitor p21. In addition, immature colon carcinoma transcript 1 silencing significantly induced non–small cell lung cancer cell apoptosis by annexin V/7-amino-actinomycin D double-staining assay. All our data suggest that immature colon carcinoma transcript 1 may play an important role for non–small cell lung cancer cell proliferation and could be a potential molecular target for diagnosing and treating human non–small cell lung cancer.
机译:尽管手术和化疗改善,但非小细胞肺癌,作为最常见的肺癌,较低的生存率为5年,尽管手术和化疗。以前的研究表明未成无状的结肠癌转录物1与人癌细胞的肿瘤鉴定密切相关。在本研究中,我们发现不成功的结肠癌转录物1在肺癌组织中过表达使用on Comcomate Data Data Data挖掘,并在非小细胞肺癌细胞系95D和A549中研究了未成无状的结肠癌转录物1的生物学效果。慢病毒介导的RNA干扰用于在体外敲低95D和A549细胞中的未成无化结肠癌转录物1表达,并且使用定量实时聚合酶链反应和Western印迹测定法测定敲低效率。未成无状的结肠癌转录物1的敲低显着抑制了3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物和菌落形成测定的非小细胞肺癌细胞增殖和菌落形成能力。施用流式细胞术以测量细胞周期停滞,结果显示在95D细胞中以G <亚/亚> / m相中停止的细胞周期,并在G 0 / g 1/549细胞中的1 相。此外,我们通过Western印迹分析测量了细胞周期相关蛋白的水平,并且发现由于细胞周期活化剂细胞周期蛋白D1的下调和细胞周期抑制剂P21的上调而出现未成无状的结肠癌转录物1介导细胞增殖抑制。此外,未成药的结肠癌转录物1沉默地通过附膜蛋白v / 7-氨基 - 辐射霉素D双染料测定显着诱导非小细胞肺癌细胞凋亡。我们所有的数据表明,未成熟的结肠癌转录物1可能对非小细胞肺癌细胞增殖发挥重要作用,并且可以是用于诊断和治疗人非小细胞肺癌的潜在分子靶标。

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