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RNA干扰与抗病毒治疗。

RNA interference and antiviral therapy.

作者信息

Ma Yan, Chan Chu-Yan, He Ming-Liang

机构信息

Stanley Ho Centre for Emerging Infectious Diseases, and Li Ka Shing Institute of Health Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.

出版信息

World J Gastroenterol. 2007 Oct 21;13(39):5169-79. doi: 10.3748/wjg.v13.i39.5169.

DOI:10.3748/wjg.v13.i39.5169
PMID:17876887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4171298/
Abstract

RNA interference (RNAi) is an evolutionally conserved gene silencing mechanism present in a variety of eukaryotic species. RNAi uses short double-stranded RNA (dsRNA) to trigger degradation or translation repression of homologous RNA targets in a sequence-specific manner. This system can be induced effectively in vitro and in vivo by direct application of small interfering RNAs (siRNAs), or by expression of short hairpin RNA (shRNA) with non-viral and viral vectors. To date, RNAi has been extensively used as a novel and effective tool for functional genomic studies, and has displayed great potential in treating human diseases, including human genetic and acquired disorders such as cancer and viral infections. In the present review, we focus on the recent development in the use of RNAi in the prevention and treatment of viral infections. The mechanisms, strategies, hurdles and prospects of employing RNAi in the pharmaceutical industry are also discussed.

摘要

RNA干扰(RNAi)是一种存在于多种真核生物物种中的进化保守基因沉默机制。RNAi利用短双链RNA(dsRNA)以序列特异性方式触发同源RNA靶标的降解或翻译抑制。通过直接应用小干扰RNA(siRNA),或通过使用非病毒和病毒载体表达短发夹RNA(shRNA),该系统可在体外和体内有效诱导。迄今为止,RNAi已被广泛用作功能基因组学研究的一种新颖且有效的工具,并在治疗人类疾病方面显示出巨大潜力,包括癌症和病毒感染等人类遗传性和后天性疾病。在本综述中,我们重点关注RNAi在预防和治疗病毒感染方面的最新进展。还讨论了在制药行业中应用RNAi的机制、策略、障碍和前景。

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本文引用的文献

1
Lentivirus-mediated RNA interference targeting enhancer of zeste homolog 2 inhibits hepatocellular carcinoma growth through down-regulation of stathmin.慢病毒介导的靶向zeste同源物2增强子的RNA干扰通过下调微管相关蛋白1轻链3抑制肝癌生长
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Clathrin-dependent entry of severe acute respiratory syndrome coronavirus into target cells expressing ACE2 with the cytoplasmic tail deleted.严重急性呼吸综合征冠状病毒通过网格蛋白依赖途径进入细胞质尾缺失的表达血管紧张素转换酶2的靶细胞。
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A tightly regulated and reversibly inducible siRNA expression system for conditional RNAi-mediated gene silencing in mammalian cells.一种用于在哺乳动物细胞中进行条件性RNA干扰介导的基因沉默的严格调控且可逆诱导的小干扰RNA表达系统。
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Comparison of RNAi efficiency mediated by tetracycline-responsive H1 and U6 promoter variants in mammalian cell lines.四环素响应性H1和U6启动子变体在哺乳动物细胞系中介导的RNAi效率比较。
Nucleic Acids Res. 2007;35(9):e67. doi: 10.1093/nar/gkm193. Epub 2007 Apr 10.
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Reversible gene knockdown in mice using a tight, inducible shRNA expression system.使用紧密、可诱导的短发夹RNA(shRNA)表达系统在小鼠中实现可逆的基因敲低。
Nucleic Acids Res. 2007;35(7):e54. doi: 10.1093/nar/gkm122. Epub 2007 Mar 21.
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Silencing of HIV-1 with RNA interference: a multiple shRNA approach.利用RNA干扰沉默HIV-1:一种多短发夹RNA方法。
Mol Ther. 2006 Dec;14(6):883-92. doi: 10.1016/j.ymthe.2006.07.007. Epub 2006 Sep 7.
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The virion-associated incoming HIV-1 RNA genome is not targeted by RNA interference.与病毒体相关的进入的HIV-1 RNA基因组不会被RNA干扰靶向。
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Silencing of HIV-1 gene expression by siRNAs in transduced cells.在转导细胞中,小干扰RNA(siRNA)使HIV-1基因表达沉默。
Nucleosides Nucleotides Nucleic Acids. 2006;25(7):795-9. doi: 10.1080/15257770600726083.
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Simultaneous targeting of HCV replication and viral binding with a single lentiviral vector containing multiple RNA interference expression cassettes.利用含有多个RNA干扰表达盒的单一慢病毒载体同时靶向丙型肝炎病毒复制和病毒结合
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