Literature DB >> 34208592

Therapy Prospects for Mitochondrial DNA Maintenance Disorders.

Javier Ramón1,2, Ferran Vila-Julià1,2, David Molina-Granada1,2, Miguel Molina-Berenguer1,2, Maria Jesús Melià1,2, Elena García-Arumí1,2, Javier Torres-Torronteras1,2, Yolanda Cámara1,2, Ramon Martí1,2.   

Abstract

Mitochondrial DNA depletion and multiple deletions syndromes (MDDS) constitute a group of mitochondrial diseases defined by dysfunctional mitochondrial DNA (mtDNA) replication and maintenance. As is the case for many other mitochondrial diseases, the options for the treatment of these disorders are rather limited today. Some aggressive treatments such as liver transplantation or allogeneic stem cell transplantation are among the few available options for patients with some forms of MDDS. However, in recent years, significant advances in our knowledge of the biochemical pathomechanisms accounting for dysfunctional mtDNA replication have been achieved, which has opened new prospects for the treatment of these often fatal diseases. Current strategies under investigation to treat MDDS range from small molecule substrate enhancement approaches to more complex treatments, such as lentiviral or adenoassociated vector-mediated gene therapy. Some of these experimental therapies have already reached the clinical phase with very promising results, however, they are hampered by the fact that these are all rare disorders and so the patient recruitment potential for clinical trials is very limited.

Entities:  

Keywords:  depletion; gene therapy; mitochondria; mtDNA; multiple deletions; nucleoside; replication; therapy

Year:  2021        PMID: 34208592     DOI: 10.3390/ijms22126447

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  4 in total

Review 1.  Gene Therapeutic Approaches for the Treatment of Mitochondrial Dysfunction in Parkinson's Disease.

Authors:  Jannik Prasuhn; Norbert Brüggemann
Journal:  Genes (Basel)       Date:  2021-11-22       Impact factor: 4.096

2.  Mice lacking the mitochondrial exonuclease MGME1 develop inflammatory kidney disease with glomerular dysfunction.

Authors:  Dusanka Milenkovic; Adrián Sanz-Moreno; Julia Calzada-Wack; Birgit Rathkolb; Oana Veronica Amarie; Raffaele Gerlini; Antonio Aguilar-Pimentel; Jelena Misic; Marie-Lune Simard; Eckhard Wolf; Helmut Fuchs; Valerie Gailus-Durner; Martin Hrabě de Angelis; Nils-Göran Larsson
Journal:  PLoS Genet       Date:  2022-05-09       Impact factor: 6.020

3.  Molecular Research on Mitochondrial Dysfunction.

Authors:  Carlo Viscomi; Maria Eugenia Soriano
Journal:  Int J Mol Sci       Date:  2022-06-20       Impact factor: 6.208

Review 4.  Inborn Errors of Nucleoside Transporter (NT)-Encoding Genes (SLC28 and SLC29).

Authors:  Marçal Pastor-Anglada; Aida Mata-Ventosa; Sandra Pérez-Torras
Journal:  Int J Mol Sci       Date:  2022-08-07       Impact factor: 6.208

  4 in total

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