Literature DB >> 29980632

Emerging therapies for mitochondrial diseases.

Michio Hirano1, Valentina Emmanuele2, Catarina M Quinzii2.   

Abstract

For the vast majority of patients with mitochondrial diseases, only supportive and symptomatic therapies are available. However, in the last decade, due to extraordinary advances in defining the causes and pathomechanisms of these diverse disorders, new therapies are being developed in the laboratory and are entering human clinical trials. In this review, we highlight the current use of dietary supplement and exercise therapies as well as emerging therapies that may be broadly applicable across multiple mitochondrial diseases or tailored for specific disorders. Examples of non-tailored therapeutic targets include: activation of mitochondrial biogenesis, regulation of mitophagy and mitochondrial dynamics, bypass of biochemical defects, mitochondrial replacement therapy, and hypoxia. In contrast, tailored therapies are: scavenging of toxic compounds, deoxynucleoside and deoxynucleotide treatments, cell replacement therapies, gene therapy, shifting mitochondrial DNA mutation heteroplasmy, and stabilization of mutant mitochondrial transfer RNAs.
© 2018 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society.

Entities:  

Keywords:  Leber Hereditary Optic Neuropathy (LHON); MELAS syndrome; mitochondrial diseases; mitophagy

Mesh:

Substances:

Year:  2018        PMID: 29980632      PMCID: PMC6104515          DOI: 10.1042/EBC20170114

Source DB:  PubMed          Journal:  Essays Biochem        ISSN: 0071-1365            Impact factor:   8.000


  103 in total

1.  MELAS and L-arginine therapy.

Authors:  Yasutoshi Koga; Yukihiro Akita; Junko Nishioka; Shuichi Yatsuga; Nataliya Povalko; Koujyu Katayama; Toyojiro Matsuishi
Journal:  Mitochondrion       Date:  2006-12-05       Impact factor: 4.160

2.  Combined treatment with oral metronidazole and N-acetylcysteine is effective in ethylmalonic encephalopathy.

Authors:  Carlo Viscomi; Alberto B Burlina; Imad Dweikat; Mario Savoiardo; Costanza Lamperti; Tatjana Hildebrandt; Valeria Tiranti; Massimo Zeviani
Journal:  Nat Med       Date:  2010-07-25       Impact factor: 53.440

3.  Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes.

Authors:  Ronghua Li; Min-Xin Guan
Journal:  Mol Cell Biol       Date:  2010-03-01       Impact factor: 4.272

4.  A systems approach for decoding mitochondrial retrograde signaling pathways.

Authors:  Sehyun Chae; Byung Yong Ahn; Kyunghee Byun; Young Min Cho; Myeong-Hee Yu; Bonghee Lee; Daehee Hwang; Kyong Soo Park
Journal:  Sci Signal       Date:  2013-02-26       Impact factor: 8.192

5.  Expression of the Ciona intestinalis alternative oxidase (AOX) in Drosophila complements defects in mitochondrial oxidative phosphorylation.

Authors:  Daniel J M Fernandez-Ayala; Alberto Sanz; Suvi Vartiainen; Kia K Kemppainen; Marek Babusiak; Eero Mustalahti; Rodolfo Costa; Tea Tuomela; Massimo Zeviani; Jongkyeong Chung; Kevin M C O'Dell; Pierre Rustin; Howard T Jacobs
Journal:  Cell Metab       Date:  2009-05       Impact factor: 27.287

6.  Liver transplant in ethylmalonic encephalopathy: a new treatment for an otherwise fatal disease.

Authors:  Carlo Dionisi-Vici; Daria Diodato; Giuliano Torre; Stefano Picca; Rosanna Pariante; Sergio Giuseppe Picardo; Ivano Di Meo; Cristiano Rizzo; Valeria Tiranti; Massimo Zeviani; Jean De Ville De Goyet
Journal:  Brain       Date:  2016-02-25       Impact factor: 13.501

7.  Clinical and biochemical improvements in a patient with MNGIE following enzyme replacement.

Authors:  Bridget E Bax; Murray D Bain; Mauro Scarpelli; Massimiliano Filosto; Paola Tonin; Nicholas Moran
Journal:  Neurology       Date:  2013-08-21       Impact factor: 9.910

8.  Long-term bezafibrate treatment improves skin and spleen phenotypes of the mtDNA mutator mouse.

Authors:  Lloye M Dillon; Aline Hida; Sofia Garcia; Tomas A Prolla; Carlos T Moraes
Journal:  PLoS One       Date:  2012-09-04       Impact factor: 3.240

9.  Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathy.

Authors:  T Klopstock; G Metz; P Yu-Wai-Man; B Büchner; C Gallenmüller; M Bailie; N Nwali; P G Griffiths; B von Livonius; L Reznicek; J Rouleau; N Coppard; T Meier; P F Chinnery
Journal:  Brain       Date:  2013-02-06       Impact factor: 13.501

10.  Development of a single-chain, quasi-dimeric zinc-finger nuclease for the selective degradation of mutated human mitochondrial DNA.

Authors:  Michal Minczuk; Monika A Papworth; Jeffrey C Miller; Michael P Murphy; Aaron Klug
Journal:  Nucleic Acids Res       Date:  2008-05-29       Impact factor: 16.971

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  37 in total

Review 1.  Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies.

Authors:  Fatima Djouadi; Jean Bastin
Journal:  Cells       Date:  2019-03-28       Impact factor: 6.600

Review 2.  Advances in primary mitochondrial myopathies.

Authors:  Isabella Peixoto de Barcelos; Valentina Emmanuele; Michio Hirano
Journal:  Curr Opin Neurol       Date:  2019-10       Impact factor: 5.710

3.  Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity.

Authors:  Rohit Sharma; Bryn Reinstadler; Kristin Engelstad; Owen S Skinner; Erin Stackowitz; Ronald G Haller; Clary B Clish; Kerry Pierce; Melissa A Walker; Robert Fryer; Devin Oglesbee; Xiangling Mao; Dikoma C Shungu; Ashok Khatri; Michio Hirano; Darryl C De Vivo; Vamsi K Mootha
Journal:  J Clin Invest       Date:  2021-01-19       Impact factor: 14.808

Review 4.  Pathophysiology of Conversion to Symptomatic Leber Hereditary Optic Neuropathy and Therapeutic Implications: a Review.

Authors:  Alvaro J Mejia-Vergara; Nicolas Seleme; Alfredo A Sadun; Rustum Karanjia
Journal:  Curr Neurol Neurosci Rep       Date:  2020-04-15       Impact factor: 5.081

Review 5.  Disease-Associated Genetic Variation in Human Mitochondrial Protein Import.

Authors:  Emmanuelle Nicolas; Rossella Tricarico; Michelle Savage; Erica A Golemis; Michael J Hall
Journal:  Am J Hum Genet       Date:  2019-05-02       Impact factor: 11.025

6.  Current progress in the therapeutic options for mitochondrial disorders.

Authors:  E Koňaříková; A Marković; Z Korandová; J Houštěk; T Mráček
Journal:  Physiol Res       Date:  2020-11-02       Impact factor: 1.881

Review 7.  Current and Emerging Clinical Treatment in Mitochondrial Disease.

Authors:  Rory J Tinker; Albert Z Lim; Renae J Stefanetti; Robert McFarland
Journal:  Mol Diagn Ther       Date:  2021-03-01       Impact factor: 4.074

Review 8.  PGC1s and Beyond: Disentangling the Complex Regulation of Mitochondrial and Cellular Metabolism.

Authors:  Lara Coppi; Simona Ligorio; Nico Mitro; Donatella Caruso; Emma De Fabiani; Maurizio Crestani
Journal:  Int J Mol Sci       Date:  2021-06-27       Impact factor: 5.923

9.  Epilepsy Associated With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes.

Authors:  Jiaai Li; Wuqiong Zhang; Zhitao Cui; Zhaoran Li; Ting Jiang; Hongmei Meng
Journal:  Front Neurol       Date:  2021-06-11       Impact factor: 4.003

10.  Minimal mitochondrial respiration is required to prevent cell death by inhibition of mTOR signaling in CoQ-deficient cells.

Authors:  Ying Wang; Siegfried Hekimi
Journal:  Cell Death Discov       Date:  2021-08-04
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