Habib Saffiya, Ariatti Mario, Singh Moganavelli
Nano-Gene and Drug Delivery Group, Discipline of Biochemistry, University of KwaZulu-Natal, Private Bag, Durban X54001, South Africa.
Biomedicines. 2020 Dec 15;8(12):612. doi: 10.3390/biomedicines8120612.
Overexpression of the proto-oncogene features prominently in most human cancers. Early studies established that inhibiting the expression of oncogenic , produced potent anti-cancer effects. This gave rise to the notion that an appropriate silencing agent might provide a broadly applicable and more effective form of cancer treatment than is currently available. The endogenous mechanism of RNA interference (RNAi), through which small RNA molecules induce gene silencing by binding to complementary mRNA transcripts, represents an attractive avenue for inhibition. However, the development of a clinically viable, anti- RNAi-based platform is largely dependent upon the design of an appropriate carrier of the effector nucleic acids. To date, organic and inorganic nanoparticles were assessed both in vitro and in vivo, as carriers of small interfering RNA (siRNA), DICER-substrate siRNA (DsiRNA), and short hairpin RNA (shRNA) expression plasmids, directed against the oncogene. We review here the various anti- RNAi-based nanosystems that have come to the fore, especially between 2005 and 2020.
原癌基因的过表达在大多数人类癌症中显著存在。早期研究表明,抑制致癌基因的表达可产生强大的抗癌效果。这引发了一种观点,即一种合适的沉默剂可能会提供一种比现有方法更广泛适用且更有效的癌症治疗形式。RNA干扰(RNAi)的内源性机制,即小RNA分子通过与互补的mRNA转录本结合来诱导基因沉默,是一种有吸引力的抑制途径。然而,基于RNAi的临床可行平台的开发很大程度上依赖于效应核酸合适载体的设计。迄今为止,有机和无机纳米颗粒已在体外和体内进行评估,作为针对致癌基因的小干扰RNA(siRNA)、Dicer底物siRNA(DsiRNA)和短发夹RNA(shRNA)表达质粒的载体。我们在此回顾自2005年至2020年间涌现的各种基于RNAi的纳米系统。