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<title cf:type="text"><![CDATA[Progress in Biochemistry and Biophysics -->Special Topic: Delivery of siRNA]]></title>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Delivery: a principal challenge in siRNA application]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20120251]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[自20世纪末RNA干扰现象(RNA interference)及其作用机制被发现以来，外源性的小干扰RNA(siRNA)已广泛地用于从基础研究到临床实践的多个领域。但，如何有效地、特异地将siRNA输送进入靶细胞，始终是使用者关注的重点，并已逐步成为siRNA应用于临床治疗的瓶颈问题之一。目前开展研究的siRNA转运方法主要包括3类：a. 通过与配基偶联实现siRNA的转运；b. 将siRNA包载于纳米颗粒等中经内吞进入细胞； c. 载体与细胞膜融合释放所载siRNA进入细胞。<br>
本刊在这期中特意选择了3篇文章组成了一个小专题来介绍与探讨siRNA的输送问题。梁伟等应邀撰写了题为《siRNA脂质纳米输送载体的研究进展》的综述，介绍了siRNA输送载体的基本要求，特别是脂质纳米载体(lipid-based siRNA delivering systems)的设计和构筑原则，以及这类载体的研发现状和应用前景；张洪杰等结合自身的研发工作撰写了《细胞穿透肽及其结构改造在siRNA传递中的应用》一文，从发现、毒副作用、传递机制、结构修饰与传递功能改进等几个方面，系统评述了细胞穿透肽(cell penetrating peptides)在siRNA传递方面研究与应用的进展；张兴梅等在《适配子介导的siRNA转运》一文中重点介绍了基于适配子(aptamer)的siRNA转运系统的转运机制、近期研究进展和应用前景。3篇文章各有侧重，反映了当前siRNA转运研究中几个比较活跃的领域的研究进展，希望能对广大读者有所帮助。]]></description>
<pubDate>2012/5/25 0:00:00</pubDate>
<category><![CDATA[Special Topic: Delivery of siRNA]]></category>
<author><![CDATA[CHEN Run-Sheng]]></author>
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<atom:name>CHEN Run-Sheng</atom:name>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Review: Lipid-based siRNA Delivery Systems]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20120190]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[RNA interference (RNAi) is a specific gene-silencing mechanism triggered by small interfering RNA (siRNA). The application of RNAi in the clinic requires the development of safe and effective delivery systems. Efforts have been dedicated to the development of lipid-based systems in siRNA deliveries. Many of the lipid-based delivery vehicles' self-assemble with siRNA are through electrostatic interactions with charged amines. Electrostatic interactions must be stable enough to sustain the nucleic payload in the carrier en route, but must allow dissociation, to execute therapeutic activity, at the delivery site. Internalization of lipid-based siRNA delivery systems into cells typically occurs through endocytosis; accordingly, delivery requires materials that can facilitate endosomal escape. The size of the carrier is important as carriers <100 nm in diameter have been reported to have higher accumulation levels in tumours, hepatocytes and inflamed tissue. To reduce RES uptake and increase circulation time, carriers have been modified on the surface with polyethyleneglycol. Herein, we review basic requirements for building lipid-based siRNA delivery systems.]]></description>
<pubDate>2012/5/25 0:00:00</pubDate>
<category><![CDATA[Special Topic: Delivery of siRNA]]></category>
<author><![CDATA[DONG Wen-Juan,ZHOU Yin-Jian and LIANG Wei]]></author>
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<atom:name>DONG Wen-Juan,ZHOU Yin-Jian and LIANG Wei</atom:name>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Review: The Effects of Cell Penetrating Peptides Structure Modification on Their siRNA Delivery Function <i>in vitro</i> and <i>in vivo</i>]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20120052]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The less of high efficient carriers to deliver siRNA drugs into their targeted tissues/cells with less toxicity are the major obstacles of siRNA pharmaceuticals in clinic application. The recent advance of siRNA delivery research based on cell-penetrating peptides (CPPs) in clinic opened the way of siRNA techniques for therapeutic application (Yi <i>et al.</i>,  <i>Mol Ther</i> (2011)19, 362-371). CPPs are short amphipathic and cationic peptides that are rapidly internalized across cell membranes. They can be used to deliver molecular cargos, such as imaging agents (fluorescent dyes and quantum dots), drugs, liposomes, peptide/protein, oligonucleotide/DNA/RNA, nanoparticles and bacteriophage into cells. The mechanism of cellular uptake and subsequent processing still remains controversial. It is now clear that CPP can mediate intracellular delivery <i>via</i> both endocytic and non-endocytic pathways. In this review, we discuss potential functions of CPPs, especially in structure modified CPPs for small RNA delivery <i>in vitro</i> and <i>in vivo</i>, highlighting their powerful promise for clinical efficacy.]]></description>
<pubDate>2012/3/19 0:00:00</pubDate>
<category><![CDATA[Special Topic: Delivery of siRNA]]></category>
<author><![CDATA[ZHANG Hong-Jie and YIN James-Qin-wei]]></author>
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<atom:name>ZHANG Hong-Jie and YIN James-Qin-wei</atom:name>
</atom:author>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Review: Aptamer Mediated Delivery of Small Interfering RNAs]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20110619]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The ability of small interfering RNA (siRNA) to inhibit mammalian gene expression is being exploited as a new class of therapeutics for a variety of diseases．However, the efficient and safe delivery of siRNAs into specific cell populations is still the principal challenge in the clinical development of RNAi therapeutics．Many potential delivery vehicles and vectors have been explored including the aptamers targeting cell surface proteins．Selected nucleic acid binding species (aptamers) are high affinity and specificity for their targets, and they have been effectively applied in targeted therapy and diagnostics of diseases．The aptamer-based delivery of siRNAs can often enhance the therapeutic efficacy and reduce the unwanted off-target effects of siRNAs．Nowadays, some kinds of aptamers are able to mediate the delivery of siRNA, such as anti-PSMA aptamer, anti-gp120 aptamer. I will review the latest progress about aptamer mediated siRNA．]]></description>
<pubDate>2012/4/23 0:00:00</pubDate>
<category><![CDATA[Special Topic: Delivery of siRNA]]></category>
<author><![CDATA[TAN Yan and ZHANG Xing-Mei]]></author>
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<atom:name>TAN Yan and ZHANG Xing-Mei</atom:name>
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