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首页> 外文期刊>World journal of gastroenterology : >WWOX induces apoptosis and inhibits proliferation of human hepatoma cell line SMMC-7721.
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WWOX induces apoptosis and inhibits proliferation of human hepatoma cell line SMMC-7721.

机译:WWOX诱导人肝癌细胞SMMC-7721凋亡并抑制其增殖。

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摘要

To investigate the effects of the WWOX gene on the human hepatic carcinoma cell line SMMC-7721.Full-length WWOX cDNA was amplified from normal human liver tissues. Full-length cDNA was subcloned into pEGFP-N1, a eukaryotic expression vector. After introduction of the WWOX gene into cancer cells using liposomes, the WWOX protein level in the cells was detected through Western blotting. Cell growth rates were assessed by methyl thiazolyl tetrazolium (MTT) and colony formation assays. Cell cycle progression and cell apoptosis were measured by flow cytometry. The phosphorylated protein kinase B (AKT) and activated fragments of caspase-9 and caspase-3 were examined by Western blotting analysis.WWOX significantly inhibited cell proliferation, as evaluated by the MTT and colony formation assays. Cells transfected with WWOX showed significantly higher apoptosis ratios when compared with cells transfected with a mock plasmid, and overexpression of WWOX delayed cell cycle progression from G1 to S phase, as measured by flow cytometry. An increase in apoptosis was also indicated by a remarkable activation of caspase-9 and caspase-3 and a dephosphorylation of AKT (Thr308 and Ser473) measured with Western blotting analysis.Overexpression of WWOX induces apoptosis and inhibits proliferation of the human hepatic carcinoma cell line SMMC-7721.
机译:为了研究WWOX基因对人肝癌细胞SMMC-7721的影响,从正常人肝组织中扩增了全长WWOX cDNA。将全长cDNA亚克隆到真核表达载体pEGFP-N1中。使用脂质体将WWOX基因导入癌细胞后,通过Western印迹检测细胞中WWOX蛋白的水平。通过甲基噻唑基四唑(MTT)和集落形成测定法评估细胞生长速率。通过流式细胞术测量细胞周期进程和细胞凋亡。蛋白质印迹法分析了磷酸化的蛋白激酶B(AKT)和caspase-9和caspase-3的活化片段.MTX和集落形成分析表明,WWOX显着抑制细胞增殖。与用模拟质粒转染的细胞相比,用WWOX转染的细胞显示出明显更高的凋亡率,并且通过流式细胞术测量,WWOX的过表达延迟了细胞周期从G1到S期的进程。 Western blotting分析显示,caspase-9和caspase-3的显着活化以及AKT的去磷酸化(Thr308和Ser473)也表明细胞凋亡增加.WWOX的过表达诱导人肝癌细胞凋亡并抑制其增殖SMMC-7721。

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