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首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Silencing of the COPS3 Gene by siRNA Reduces Proliferation of Lung Cancer Cells Most Likely via induction of Cell Cycle Arrest and Apoptosis
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Silencing of the COPS3 Gene by siRNA Reduces Proliferation of Lung Cancer Cells Most Likely via induction of Cell Cycle Arrest and Apoptosis

机译:SiRNA的COPS3基因的沉默可通过诱导细胞周期骤停和细胞凋亡来减少肺癌细胞的增殖

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The COPS3 gene has stimulating effect on cell proliferation and progression of osteosarcomas and related cells. However, the features of COPS3 and its potential application as a therapeutic target in other cancers has not yet been studied. In this study, therefore, the effect of COPS3 silencing via COPS3 siRNA on lung cancer cell proliferation was examined. Expression levels of COPS3 gene in COPS3 siRNA infected cells and control siRNA infected cells were compared with real time PCR and Western blot analysis. Cell proliferation levels were comprehensively analyzed by MTT, BrdU incorporationy, and colony formation assays. For mechanistic assessment the effects of COPS3 silencing on cell cycle and apoptosis were analyzed using flow cytometry. Results showed that successful silencing of the COPS3 gene at both translational and transcriptional levels significantly reduced the proliferation and colony formation by lung cancer cells (p0.01). Flow cytometry showed cell cycle arrest in the G0/G1 phase after COPS3 silencing, and more importantly, apoptosis was induced as a result of COPS3 knockdown, which negatively affected cell survival. Therefore, these results provide another piece of important evidence that the COPS3 gene expressed in lung cancer cells may play a critical role in stimulating proliferation. Down-regulation of COPS3 could significantly inhibit lung cancer cell growth, which was most likely mediated via induction of cell cycle arrest in G0/G1 phase and apoptosis.
机译:COPS3基因对细胞增殖和骨肉瘤和相关细胞进行的影响刺激了刺激。然而,尚未研究COPS3的特征及其作为其他癌症治疗靶标的潜在应用。因此,在该研究中,检查了COPS3沉默的COPS3 siRNA对肺癌细胞增殖的影响。将COPS3 SiRNA感染细胞中COPS3基因的表达水平与实时PCR和Western印迹分析进行比较。通过MTT,BRDU IncloudAly和菌落形成测定综合分析细胞增殖水平。为了机械评估,使用流式细胞术分析COPS3沉默对细胞周期和细胞凋亡的影响。结果表明,在平移和转录水平下,COPS3基因的成功沉默显着降低了肺癌细胞的增殖和菌落形成(P <0.01)。流式细胞术显示COPS3沉默后G0 / G1相中的细胞周期停滞,更重要的是,由于COPS3敲低而导致细胞凋亡,对细胞存活产生负面影响。因此,这些结果提供了另一种重要证据,即肺癌细胞中表达的COPS3基因可能在刺激增殖中发挥关键作用。 COPS3的下调可显着抑制肺癌细胞生长,最可能通过诱导G0 / G1相和细胞凋亡诱导细胞周期骤停介导。

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