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Adv Pharm Bull. 2017;7(4): 603-609.
doi: 10.15171/apb.2017.072
PMID: 29399550
PMCID: PMC5788215
Scopus ID: 85043385514
  Abstract View: 2271
  PDF Download: 1792

Research Article

Strategies for Improving siRNA-Induced Gene Silencing Efficiency

Fatemeh Safari 1,2,3*, Solmaz Rahmani Barouji 4, Ali Mohammad Tamaddon 5

1 Medical Biotechnology Department, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
2 Shiraz University of Medical Sciences, Shiraz, Iran.
3 Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
4 Department of Traditional Medicine, Faculty of Traditional Medicine, University of Medical Sciences, Tabriz, Iran.
5 Center for Pharmaceutical Nanotechnology and Biomaterials, Faculty of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
*Corresponding Author: Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran. Email safarif@tbzmed.ac.ir
*Corresponding Author: Email: safarif@tbzmed.ac.ir

Abstract

Purpose: Human telomerase reverse transcriptase (hTERT) plays a crucial role in tumorigenesis and progression of cancers. Gene silencing of hTERT by short interfering RNA (siRNA) is considered as a promising strategy for cancer gene therapy. Various algorithms have been devised for designing a high efficient siRNA which is a significant issue in the clinical usage. Thereby, in the present study, the relation of siRNA designing criteria and the gene silencing efficiency was evaluated. Methods: The siRNA sequences were designed and characterized by using on line soft wares. Cationic co-polymer (polyethylene glycol-g-polyethylene imine (PEG-g-PEI)) was used for the construction of polyelectrolyte complexes (PECs) containing siRNAs. The cellular uptake of the PECs was evaluated. The gene silencing efficiency of different siRNA sequences was investigated and the effect of observing the rational designing on the functionality of siRNAs was assessed. Results: The size of PEG-g-PEI siRNA with N/P (Nitrogen/Phosphate) ratio of 2.5 was 114 ± 0.645 nm. The transfection efficiency of PECs was desirable (95.5% ± 2.4%.). The results of Real-Time PCR showed that main sequence (MS) reduced the hTERT expression up to 90% and control positive sequence (CPS) up to 63%. These findings demonstrated that the accessibility to the target site has priority than the other criteria such as sequence preferences and thermodynamic features. Conclusion: siRNA opens a hopeful window in cancer therapy which provides a convenient and tolerable therapeutic approach. Thereby, using the set of criteria and rational algorithms in the designing of siRNA remarkably affect the gene silencing efficiency.
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Submitted: 18 Jul 2017
Revision: 24 Oct 2017
Accepted: 25 Oct 2017
ePublished: 31 Dec 2017
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