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Efficient Inhibition of Human Immunodeficiency Virus Replication Using Novel Modified Microrna-30A Targeting 3'-Untranslated Region Transcripts Publisher



Nejati A1 ; Shahmahmoodi S1 ; Arefian E2, 3 ; Shoja Z4 ; Marashi SM1 ; Tabatabaie H1 ; Mollaeikandelous Y5 ; Soleimani M3, 6 ; Nategh R1
Authors
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Authors Affiliations
  1. 1. Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, 14716-13151, Iran
  2. 2. Biotechnology Center, College of Science, University of Tehran, Tehran, 14176-14411, Iran
  3. 3. Department of Molecular Biology and Genetic Engineering, Stem Cell Technology Research Center, Tehran, 19977-75555, Iran
  4. 4. Virology Department, Pasteur Institute of Iran, Tehran, 13169-43551, Iran
  5. 5. Immunology Department, Iran University of Medical Science, Tehran, 14716-13151, Iran
  6. 6. Department of Medical Physics, Tarbiat Modares University, Tehran, 14117-13116, Iran

Source: Experimental and Therapeutic Medicine Published:2016


Abstract

RNA interference (RNAi)-based gene therapy is currently considered to be a combinatorial anti-human immunodeficiency virus-1 (HIV-1) therapy. Although arti­ficial polycistronic microRNAs (miRs) can reduce HIV-1 escape mutant variants, this approach may increase the risk of side effects. The present study aimed to optimize the efficiency of anti-HIV RNAi gene therapy in order to reduce the cell toxicity induced by multi-short hairpin RNA expression. An artificial miR-30a-3'-untranslated region (miR-3'-UTR) obtained from a single RNA polymerase II was used to simultaneously target all viral transcripts. The results of the present study demonstrated that HIV-1 replication was signifi­cantly inhibited in the cells with the miR-3'-UTR construct, suggesting that miR-3'-UTR may serve as a promising tool for RNAi-based gene therapy in the treatment of HIV-1. © 2016, Spandidos Publications. All Rights Reserved.