Department of Life Science, School of Basic Science & Research, Sharda University, Greater Noida, India.
Department of Biotechnology, School of Engineering & Technology, Sharda University, Greater Noida, India.
Cancer Rep (Hoboken). 2020 Oct;3(5):e1271. doi: 10.1002/cnr2.1271. Epub 2020 Jul 30.
Drug delivery system is a common practice in cancer treatment. RNA interference-mediated post-transcriptional gene silencing holds promise as an approach to knockdown in the expression of target genes responsible for cancer cell growth and metastasis. RNA interference (RNAi) can be achieved by delivering small interfering RNA (siRNA) and short hairpin RNA (shRNA) to target cells. Since neither interfering RNAs can be delivered in naked form due to poor stability, an efficient delivery system is required that protects, guides, and delivers the siRNA and shRNA to target cells as part of cancer therapy (chemotherapy).
In this review, a discussion is presented about the different types of drug delivery system used to deliver siRNA and shRNA, together with an overview of the potential benefits associated with this sophisticated biomolecular therapy. Improved understanding of the different approaches used in nanoparticle (NP) fabrication, along with an enhanced appreciation of the biochemical properties of siRNA/shRNA, will assist in developing improved drug delivery strategies in basic and clinical research.
These novel delivery techniques are able to solve the problems that form an inevitable part of delivering genes in more efficient manner and as part of more effective treatment protocols. The present review concludes that the nanoparticulate RNA delivery system has great possibility for cancer treatment along with several other proposed methods. Several NPs or nanocarriers are already in use, but the methods proposed here could fulfill the missing gap in cancer research. It is the future technology, which unravels the mystery of resolving genomic diseases that is, especially genomic instability and its signaling cascades.
药物输送系统是癌症治疗中的常见做法。RNA 干扰介导的转录后基因沉默有望成为一种方法,用于敲低负责癌细胞生长和转移的靶基因的表达。RNA 干扰 (RNAi) 可以通过向靶细胞递送小干扰 RNA (siRNA) 和短发夹 RNA (shRNA) 来实现。由于干扰 RNA 本身由于稳定性差而不能以裸露形式递送到细胞内,因此需要一种有效的输送系统,该系统可以保护、引导和输送 siRNA 和 shRNA 作为癌症治疗(化疗)的一部分到靶细胞。
在这篇综述中,讨论了用于递送 siRNA 和 shRNA 的不同类型的药物输送系统,以及与这种复杂的生物分子治疗相关的潜在益处的概述。对纳米颗粒 (NP) 制造中使用的不同方法的理解的提高,以及对 siRNA/shRNA 的生化特性的增强认识,将有助于在基础和临床研究中开发改进的药物输送策略。
这些新型的给药技术能够解决以更有效的方式传递基因并作为更有效治疗方案的一部分所不可避免的问题。本综述认为,纳米颗粒 RNA 输送系统具有很大的潜力用于癌症治疗,以及其他几种提出的方法。已经有几种 NPs 或纳米载体在使用,但这里提出的方法可以填补癌症研究中的空白。这是未来的技术,它揭示了解决基因组疾病的奥秘,特别是基因组不稳定性及其信号级联。