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首页> 外文期刊>Pathology oncology research: POR >High Expression of PhospholipaseD2 Induced by Hypoxia Promotes Proliferation of Colon Cancer Cells through Activating NF-Bp65 Signaling Pathway
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High Expression of PhospholipaseD2 Induced by Hypoxia Promotes Proliferation of Colon Cancer Cells through Activating NF-Bp65 Signaling Pathway

机译:缺氧诱导的磷脂纤维素2的高表达通过激活NF-BP65信号通路来促进结肠癌细胞的增殖

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Hypoxia is a typical feature of colon cancer occurrence and progression. We have reported that high expression and activity of PhospholipaseD2 (PLD2) induced by hypoxia in colon cancer cells. In order to further investigate the role of PLD2 in colon cancer under hypoxic conditions. MTT assay was used to detect the proliferation of human colon cancer cells (SW480 and SW620) under hypoxic conditions by decrease the PLD2 gene expression or inhibit the activity of PLD2. Expression level of p-P65/T-P65 and Cyclin D1 were detected in those cells treated as above through using western blot and RT-PCR analysis. Effect of NF-Bp65 inhibitor (BAY-117082) on the proliferation and expression level of Cyclin D1 and PLD2 of colon cancer cells under hypoxic conditions were further analysised. As a result, decreased the expression of PLD2 or inhibited the activity of PLD2 leaded to the proliferation of hypoxia colon cancer cells reduced, and along with the expression level of p-P65/T-P65 and Cyclin D1 reduced. However, inhibition the expression level of p-P65/T-P65 lead to the proliferation and expression of Cyclin D1 in those hypoxia colon cancer cells also reduced. In vivo growth decreased in response to PLD2 and NF-Bp65 inhibition. Our study indicates that high expression of PLD2 induced by hypoxia promotes the proliferation of colon cancer cells, and it may elevate the expression level of Cyclin D1 through activating NF-Bp65 signaling pathway. Inhibition of the PLD2 expression may provide a new clue for treatment for colon cancer.
机译:缺氧是结肠癌发生和进展的典型特征。据报道,在结肠癌细胞中缺氧诱导的磷脂磷脂2(PLD2)的高表达和活性。为了进一步研究PLD2在缺氧条件下CONON癌症的作用。 MTT测定用于通过降低PLD2基因表达或抑制PLD2的活性,检测人结肠癌细胞(SW480和SW620)的增殖。通过使用Western印迹和RT-PCR分析在如上处理的那些细胞中检测到P-P65 / T-P65和细胞周期蛋白D1的表达水平。 NF-BP65抑制剂(Bay-117082)对缺氧条件下的结肠蛋白D1和结肠癌细胞的增殖和表达水平的影响进行了进一步分析。结果,降低了PLD2的表达或抑制PLD2的活性,导致缺氧结肠癌细胞的增殖降低,以及P-P65 / T-P65和Cyclin D1的表达水平降低。然而,抑制p-p65 / t-p65的表达水平导致细胞周期蛋白D1在那些缺氧结肠癌细胞中的增殖和表达也降低。响应于PLD2和NF-BP65抑制,体内增长降低。我们的研究表明,缺氧诱导的PLD2的高表达促进结肠癌细胞的增殖,并且它可以通过激活NF-BP65信号传导途径升高Cyclin D1的表达水平。对PLD2表达的抑制可以提供用于治疗结肠癌的新线索。

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