Tan Ping-Heng, Yang Lin-Cheng, Ji Ru-Rong
Department of Anesthesiology, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Open Pain J. 2009 Jan 1;2:57-63. doi: 10.2174/1876386300902010057.
In recent years RNA interference (RNAi) has rapidly become the most widely used tool for gene knockdown due to its high specificity and potency. RNAi is an evolutionarily conserved mechanism for silencing gene expression by targeted degradation of mRNA. In the past decade, hundreds of molecular targets have been identified for their roles in pain modulation. But most molecular targets are not readily druggable with small molecules. RNAi represents a therapeutic approach applicable to these non-druggable targets. There is a rapid increase in the number of studies that use small interfering RNAs (siRNAs) to validate new targets for pain regulation. In this review, we will discuss these pain-related RNAi studies (Table 1). We will also compare the advantages and disadvantages of RNAi with antisense knockdown (Table 2), because antisense oligodeoxynucleotides have been extensively used for target validation in pain research. Although in vivo delivery of siRNA remains to be a challenge, RNAi has a great potential to become a major therapeutic tool for pain management.
近年来,RNA干扰(RNAi)因其高特异性和高效性,迅速成为应用最为广泛的基因敲低工具。RNAi是一种通过靶向降解mRNA来沉默基因表达的进化保守机制。在过去十年中,已有数百个分子靶点被确定在疼痛调节中发挥作用。但大多数分子靶点难以用小分子药物靶向作用。RNAi为这些难以成药的靶点提供了一种治疗方法。使用小干扰RNA(siRNA)来验证疼痛调节新靶点的研究数量迅速增加。在本综述中,我们将讨论这些与疼痛相关的RNAi研究(表1)。我们还将比较RNAi与反义敲低的优缺点(表2),因为反义寡脱氧核苷酸已广泛用于疼痛研究中的靶点验证。尽管siRNA的体内递送仍然是一个挑战,但RNAi极有可能成为疼痛管理的主要治疗工具。