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针对生存素基因的甲基化寡核苷酸诱导非小细胞肺癌细胞凋亡。

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

机构信息

School of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Cancer Gene Ther. 2010 Jun;17(6):441-6. doi: 10.1038/cgt.2009.82. Epub 2010 Jan 22.

Abstract

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.

摘要

Survivin 过表达与肺癌发生密切相关。通过分子拮抗剂沉默 survivin 基因已显示出作为新型抗癌策略的潜力。DNA 甲基化是一种关键的表观遗传修饰,可沉默基因转录。在这项研究中,我们使用了一种新的甲基化寡核苷酸,它可介导细胞中序列特异性的 DNA 甲基化,作为针对 survivin 的治疗的一种策略替代,并研究了其在抑制 NCI-H460 细胞中 survivin 表达和随后诱导细胞凋亡的潜力。显示甲基化的有义寡核苷酸 SurKex1 可特异性降低 survivin mRNA 表达并诱导细胞凋亡。此外,人们推测甲基化寡核苷酸通过激活 DNA 甲基转移酶 (DNMT1) 发挥其基因沉默作用,但确切机制尚不清楚。我们的数据首次表明,SurKex1 通过激活 DNMT1 对 survivin 表达发挥其下调作用。

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