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Induction of apoptosis of non-small cell lung cancer by a methylated oligonucleotide targeting survivin gene

机译:靶向survivin基因的甲基化寡核苷酸诱导非小细胞肺癌细胞凋亡

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摘要

Survivin overexpression is closely linked to lung oncogenesis. Silencing of survivin gene by molecular antagonists has shown promise as novel anticancer strategies. DNA methylation is a critical epigenetic modification that silences gene transcription. In this study, we used a new methylated oligonucleotide, which mediates sequence-specific DNA methylation in cell, as a strategic alternative to survivin-targeting treatment, and investigated its efficacy in suppressing survivin expression and the consequent apoptotic induction potential in NCI-H460 cells. SurKex1, a methylated sense oligonucleotide, was shown to reduce specifically survivin mRNA expression and induce cell apoptosis. In addition, it has been supposed that the methylated oligonucleotide exerts its effect of gene silencing through the activation of DNA methyltransferase (DNMT1), but the exact mechanism is still unknown. Our data suggest for the first time that the SurKex1 exerts its down-regulatory effects on survivin expression through the activation of DNMT1.
机译:Survivin过表达与肺癌发生密切相关。分子拮抗剂沉默survivin基因已显示出作为新的抗癌策略的希望。 DNA甲基化是使基因转录沉默的重要表观遗传修饰。在这项研究中,我们使用了一种新的甲基化寡核苷酸来介导细胞中的序列特异性DNA甲基化,作为Survivin靶向治疗的战略选择,并研究了其抑制Survivin表达的功效以及随之而来的NCI-H460细胞的凋亡诱导潜力。 。 SurKex1,一种甲基化的有义寡核苷酸,显示出特异性降低survivin mRNA表达并诱导细胞凋亡。另外,据认为甲基化的寡核苷酸通过激活DNA甲基转移酶(DNMT1)发挥其基因沉默的作用,但是确切的机制仍是未知的。我们的数据首次表明SurKex1通过激活DNMT1对survivin表达发挥下调作用。

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