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Long Double-Stranded RNA-Mediated RNA Interference and Immunostimulation: Long Interfering Double-Stranded RNA as a Potent Anticancer Therapeutics

机译:长双链RNA介导的RNA干扰和免疫刺激:长干扰双链RNA作为有效的抗癌治疗药物。

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摘要

In most applications, small interfering RNAs are designed to execute specific gene silencing via RNA interference (RNAi) without triggering nonspecific responses such as immunostimulation. However, in anticancer therapeutics, immunostimulation combined with specific oncogene silencing could be beneficial, resulting in the synergistic inhibition of cancer cell growth. In this study, we report an immunostimulatory long doublestranded RNA (dsRNA) structure with the ability to trigger RNAi-mediated specific target gene silencing, termed as long interfering dsRNA (liRNA). HRNA targeting Survivin mRNA not only efficiently and specifically triggered target gene silencing via RNAi, but also stimulated the protein kinase R pathway to induce the expression ofinterferon beta. As a result, the ability of Survivin-targeting liRNA to inhibit cancer cell growth was superior over conventional small interfering RNA or nontargeting dsRNA structures. Our results thus provide a simple yet efficient dual function immunostimulatory RNAi-triggering structure, which is potentially applicable for the development of anticancer therapeutics.
机译:在大多数应用中,小型干扰RNA被设计为通过RNA干扰(RNAi)执行特定的基因沉默,而不会触发非特异性反应,例如免疫刺激。然而,在抗癌治疗中,免疫刺激与特定的癌基因沉默相结合可能是有益的,从而导致癌细胞生长的协同抑制。在这项研究中,我们报告了一种免疫刺激性长双链RNA(dsRNA)结构,具有触发RNAi介导的特异性靶基因沉默的能力,称为长干扰dsRNA(liRNA)。靶向Survivin mRNA的HRNA不仅有效且特异性地通过RNAi触发了靶基因沉默,而且还刺激了蛋白激酶R途径诱导干扰素β的表达。结果,靶向Survivin的liRNA抑制癌细胞生长的能力优于常规的小干扰RNA或非靶向dsRNA结构。因此,我们的结果提供了一种简单而有效的双重功能免疫刺激性RNAi触发结构,该结构可能适用于抗癌治疗药物的开发。

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