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首页> 外文期刊>Cancer gene therapy >Triplex-forming oligodeoxynucleotides targeting survivin inhibit proliferation and induce apoptosis of human lung carcinoma cells
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Triplex-forming oligodeoxynucleotides targeting survivin inhibit proliferation and induce apoptosis of human lung carcinoma cells

机译:靶向survivin的三链形成寡聚脱氧核苷酸抑制人肺癌细胞增殖并诱导其凋亡

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摘要

Survivin is expressed in most cancers but is undetectable in differentiated adult cells, and plays an important role both in the suppression of apoptosis and mitotic spindle checkpoint; thus it has attracted great interest as a potential drug target. In this study, we investigated the antigene and antiproliferative effects of triplex-forming oligodeoxynucleotides (TFO) targeting survivin in human lung carcinoma A549 cells. Survivin-specific TFOs form stable triplexes under physiological conditions as tested by electrophoretic mobility shift assays. Treatment of A549 cells with survivin-specific but not control TFOs at a concentration of 400nM in the presence of uptake-enhancing liposome significantly reduced survivin protein level, inhibited cell proliferation, and induced cell apoptosis as demonstrated by immunoblot, cell number counting, and Annexin V-staining. Moreover, we found that the triplex-forming potential of TFOs measured in vitro does not necessarily correlate with the ability of TFOs to affect expression of a targeted gene in vivo. Our results indicate that targeting survivin is a promising alternative strategy for the development of novel anticancer therapeutics.
机译:Survivin在大多数癌症中都有表达,但在分化的成年细胞中却无法检测到,在抑制细胞凋亡和有丝分裂纺锤体检查点中都起着重要作用。因此,作为潜在的药物靶标引起了极大的兴趣。在这项研究中,我们调查了靶向survivin的三链体形成寡脱氧核苷酸(TFO)在人肺癌A549细胞中的抗原性和抗增殖作用。 Survivin特异性TFO在生理条件下形成稳定的三链体,如电泳迁移率变动分析所测试。如免疫印迹,细胞计数和膜联蛋白所证实,在摄取增强脂质体存在下,以400nM浓度的survivin特异性但非对照TFO处理A549细胞可显着降低survivin蛋白水平,抑制细胞增殖并诱导细胞凋亡。 V型染色。此外,我们发现,在体外测量的TFO的三链体形成潜力不一定与TFO在体内影响靶基因表达的能力相关。我们的结果表明,靶向survivin是开发新型抗癌疗法的有前途的替代策略。

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