Literature DB >> 33579937

The special considerations of gene therapy for mitochondrial diseases.

Jesse Slone1, Taosheng Huang2.   

Abstract

The recent success of gene therapy across multiple clinical trials has inspired a great deal of hope regarding the treatment of previously intractable genetic diseases. This optimism has been extended to the prospect of gene therapy for mitochondrial disorders, which are not only particularly severe but also difficult to treat. However, this hope must be tempered by the reality of the mitochondrial organelle, which possesses specific biological properties that complicate genetic manipulation. In this perspective, we will discuss some of these complicating factors, including the unique pathways used to express and import mitochondrial proteins. We will also present some ways in which these challenges can be overcome by genetic manipulation strategies tailored specifically for mitochondrial diseases.

Year:  2020        PMID: 33579937     DOI: 10.1038/s41525-020-0116-5

Source DB:  PubMed          Journal:  NPJ Genom Med        ISSN: 2056-7944            Impact factor:   8.617


  62 in total

Review 1.  Insertion of proteins into the inner membrane of mitochondria: the role of the Oxa1 complex.

Authors:  Rosemary Stuart
Journal:  Biochim Biophys Acta       Date:  2002-09-02

Review 2.  Mitochondrial protein import: common principles and physiological networks.

Authors:  Jan Dudek; Peter Rehling; Martin van der Laan
Journal:  Biochim Biophys Acta       Date:  2012-06-07

Review 3.  Co-translational membrane insertion of mitochondrially encoded proteins.

Authors:  Martin Ott; Johannes M Herrmann
Journal:  Biochim Biophys Acta       Date:  2009-12-02

Review 4.  YidC/Alb3/Oxa1 Family of Insertases.

Authors:  Seth W Hennon; Raunak Soman; Lu Zhu; Ross E Dalbey
Journal:  J Biol Chem       Date:  2015-05-06       Impact factor: 5.157

Review 5.  Gene Therapy.

Authors:  Katherine A High; Maria G Roncarolo
Journal:  N Engl J Med       Date:  2019-08-01       Impact factor: 91.245

6.  Man is not alone.

Authors:  E Charry
Journal:  Pa Med       Date:  1968-12

7.  Oxa1p acts as a general membrane insertion machinery for proteins encoded by mitochondrial DNA.

Authors:  K Hell; W Neupert; R A Stuart
Journal:  EMBO J       Date:  2001-03-15       Impact factor: 11.598

8.  Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia.

Authors:  Alexis A Thompson; Mark C Walters; Janet Kwiatkowski; John E J Rasko; Jean-Antoine Ribeil; Suradej Hongeng; Elisa Magrin; Gary J Schiller; Emmanuel Payen; Michaela Semeraro; Despina Moshous; Francois Lefrere; Hervé Puy; Philippe Bourget; Alessandra Magnani; Laure Caccavelli; Jean-Sébastien Diana; Felipe Suarez; Fabrice Monpoux; Valentine Brousse; Catherine Poirot; Chantal Brouzes; Jean-François Meritet; Corinne Pondarré; Yves Beuzard; Stany Chrétien; Thibaud Lefebvre; David T Teachey; Usanarat Anurathapan; P Joy Ho; Christof von Kalle; Morris Kletzel; Elliott Vichinsky; Sandeep Soni; Gabor Veres; Olivier Negre; Robert W Ross; David Davidson; Alexandria Petrusich; Laura Sandler; Mohammed Asmal; Olivier Hermine; Mariane De Montalembert; Salima Hacein-Bey-Abina; Stéphane Blanche; Philippe Leboulch; Marina Cavazzana
Journal:  N Engl J Med       Date:  2018-04-19       Impact factor: 91.245

Review 9.  Beta-thalassemia.

Authors:  Renzo Galanello; Raffaella Origa
Journal:  Orphanet J Rare Dis       Date:  2010-05-21       Impact factor: 4.123

Review 10.  Human mitochondrial DNA: roles of inherited and somatic mutations.

Authors:  Eric A Schon; Salvatore DiMauro; Michio Hirano
Journal:  Nat Rev Genet       Date:  2012-12       Impact factor: 53.242

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