首页> 外文期刊>International journal of oncology >Optimal sequence of antisense DNA to silence YB-1 in lung cancer by use of a novel polysaccharide drug delivery system
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Optimal sequence of antisense DNA to silence YB-1 in lung cancer by use of a novel polysaccharide drug delivery system

机译:利用新型多糖药物递送系统沉默YB-1的反义DNA最佳序列

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摘要

Silencing Y-box binding protein 1 (YB-1) can be an excellent target for cancer therapy and many lung cancer cells express the polysaccharide-recognition receptor Dectin-1. We designed a Dectin-1 targeting vehicle delivering YB-1-antisense DNA. First, we selected five optimal antisense DNA sequences to silence YB-1 from among 153 candidates. We chose the sequence closest to the start codon (AS014), and attached dA40 to the 3' end; dA40 promotes complex formation with a β-(1?3)-d-glucan called schizophyllan (SPG). The resultant complexes were applied to 12 human-oriented lung cancer cell lines, and cell viability was examined. The cell lines exhibited decreased viability and showed strong affinity to bind SPG, suggesting the AS014/SPG complex entered the cells via the Dectin-1 mediated pathway.
机译:沉默Y-box结合蛋白1(YB-1)可以成为癌症治疗的理想靶标,许多肺癌细胞表达多糖识别受体Dectin-1。我们设计了可传递YB-1-反义DNA的Dectin-1靶向载体。首先,我们从153个候选基因中选择了五个最佳的反义DNA序列来沉默YB-1。我们选择最接近起始密码子的序列(AS014),并将dA40连接到3'末端。 dA40促进与称为schizophyllan(SPG)的β-(1?3)-d-葡聚糖的复合物形成。将所得复合物应用于12种以人为导向的肺癌细胞系,并检查细胞活力。细胞系表现出降低的生存力并显示出强大的结合SPG的亲和力,表明AS014 / SPG复合物通过Dectin-1介导的途径进入细胞。

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