Literature DB >> 26264709

Therapy for dominant inherited diseases by allele-specific RNA interference: successes and pitfalls.

Delphine Trochet, Bernard Prudhon, Stéphane Vassilopoulos, Marc Bitoun1.   

Abstract

RNA interference (RNAi) is a conserved mechanism for post-transcriptional gene silencing mediated by messenger RNA (mRNA) degradation. RNAi is commonly induced by synthetic siRNA or shRNA which recognizes the targeted mRNA by base pairing and leads to target-mRNA degradation. RNAi may discriminate between two sequences only differing by one nucleotide conferring a high specificity of RNAi for its target mRNA. This property was used to develop a particular therapeutic strategy called "allele-specific-RNA interference" devoted to silence the mutated allele of genes causing dominant inherited diseases without affecting the normal allele. Therapeutic benefit was now demonstrated in cells from patients and animal models, and promising results of the first phase Ib clinical trial using siRNA-based allele-specific therapy were reported in Pachyonychia Congenita, an inherited skin disorder due to dominant mutations in the Keratin 6 gene. Our purpose is to review the successes of this strategy aiming to treat dominant inherited diseases and to highlight the pitfalls to avoid.

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Year:  2015        PMID: 26264709     DOI: 10.2174/1566523215666150812115730

Source DB:  PubMed          Journal:  Curr Gene Ther        ISSN: 1566-5232            Impact factor:   4.391


  10 in total

1.  Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome Keratinocytes.

Authors:  Ming Yang Lee; Hong-Zhan Wang; Thomas W White; Tony Brooks; Alan Pittman; Heerni Halai; Anastasia Petrova; Diane Xu; Stephen L Hart; Veronica A Kinsler; Wei-Li Di
Journal:  J Invest Dermatol       Date:  2019-11-06       Impact factor: 8.551

2.  Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector.

Authors:  Artur V Cideciyan; Raghavi Sudharsan; Valérie L Dufour; Michael T Massengill; Simone Iwabe; Malgorzata Swider; Brianna Lisi; Alexander Sumaroka; Luis Felipe Marinho; Tatyana Appelbaum; Brian Rossmiller; William W Hauswirth; Samuel G Jacobson; Alfred S Lewin; Gustavo D Aguirre; William A Beltran
Journal:  Proc Natl Acad Sci U S A       Date:  2018-08-20       Impact factor: 11.205

Review 3.  Using human genetics to improve safety assessment of therapeutics.

Authors:  Keren J Carss; Aimee M Deaton; Alberto Del Rio-Espinola; Dorothée Diogo; Mark Fielden; Diptee A Kulkarni; Jonathan Moggs; Peter Newham; Matthew R Nelson; Frank D Sistare; Lucas D Ward; Jing Yuan
Journal:  Nat Rev Drug Discov       Date:  2022-10-19       Impact factor: 112.288

4.  Oxidative stress and dysfunctional NRF2 underlie pachyonychia congenita phenotypes.

Authors:  Michelle L Kerns; Jill M C Hakim; Rosemary G Lu; Yajuan Guo; Andreas Berroth; Roger L Kaspar; Pierre A Coulombe
Journal:  J Clin Invest       Date:  2016-05-16       Impact factor: 14.808

5.  ASPsiRNA: A Resource of ASP-siRNAs Having Therapeutic Potential for Human Genetic Disorders and Algorithm for Prediction of Their Inhibitory Efficacy.

Authors:  Isha Monga; Abid Qureshi; Nishant Thakur; Amit Kumar Gupta; Manoj Kumar
Journal:  G3 (Bethesda)       Date:  2017-09-07       Impact factor: 3.154

6.  Allele-Specific CRISPR/Cas9 Correction of a Heterozygous DNM2 Mutation Rescues Centronuclear Myopathy Cell Phenotypes.

Authors:  Aymen Rabai; Léa Reisser; Bernardo Reina-San-Martin; Kamel Mamchaoui; Belinda S Cowling; Anne-Sophie Nicot; Jocelyn Laporte
Journal:  Mol Ther Nucleic Acids       Date:  2019-02-27

7.  Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy.

Authors:  Delphine Trochet; Bernard Prudhon; Lylia Mekzine; Mégane Lemaitre; Maud Beuvin; Laura Julien; Sofia Benkhelifa-Ziyyat; Mai Thao Bui; Norma Romero; Marc Bitoun
Journal:  Mol Ther Nucleic Acids       Date:  2022-02-13       Impact factor: 8.886

8.  Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations.

Authors:  Swati Dudhal; Lylia Mekzine; Bernard Prudhon; Karishma Soocheta; Bruno Cadot; Kamel Mamchaoui; Delphine Trochet; Marc Bitoun
Journal:  Mol Ther Nucleic Acids       Date:  2022-08-13       Impact factor: 10.183

Review 9.  Curative Cell and Gene Therapy for Osteogenesis Imperfecta.

Authors:  Aaron Schindeler; Lucinda R Lee; Alexandra K O'Donohue; Samantha L Ginn; Craig F Munns
Journal:  J Bone Miner Res       Date:  2022-04-17       Impact factor: 6.390

10.  Allele-specific silencing therapy for Dynamin 2-related dominant centronuclear myopathy.

Authors:  Delphine Trochet; Bernard Prudhon; Maud Beuvin; Cécile Peccate; Stéphanie Lorain; Laura Julien; Sofia Benkhelifa-Ziyyat; Aymen Rabai; Kamel Mamchaoui; Arnaud Ferry; Jocelyn Laporte; Pascale Guicheney; Stéphane Vassilopoulos; Marc Bitoun
Journal:  EMBO Mol Med       Date:  2018-02       Impact factor: 12.137

  10 in total

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