Literature DB >> 19026744

A critical approach to the therapy of mitochondrial respiratory chain and oxidative phosphorylation diseases.

Salvatore Dimauro1, Pierre Rustin.   

Abstract

Taking advantage of a series of questions raised by an association of patients with mitochondrial disease, this review, after a brief overview of basic concepts of mitochondrial bioenergetics and genetics, discusses the pros and cons of a number of practical options in the field of mitochondrial therapy. This makes it clear that, in contrast to the spectacular progress in our understanding of the biochemical and molecular bases of the mitochondrial diseases defined restrictively as disorders due to defects in the mitochondrial respiratory chain, we are still extremely limited in our ability to treat these conditions. We finally discussed the emerging genetic-based strategies that show some promise, even if much work remains to be done.

Entities:  

Mesh:

Year:  2008        PMID: 19026744     DOI: 10.1016/j.bbadis.2008.10.015

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  28 in total

Review 1.  Mitochondrial medicine: to a new era of gene therapy for mitochondrial DNA mutations.

Authors:  Hélène Cwerman-Thibault; José-Alain Sahel; Marisol Corral-Debrinski
Journal:  J Inherit Metab Dis       Date:  2010-06-23       Impact factor: 4.982

2.  Pharmacologic modeling of primary mitochondrial respiratory chain dysfunction in zebrafish.

Authors:  James Byrnes; Rebecca Ganetzky; Richard Lightfoot; Michael Tzeng; Eiko Nakamaru-Ogiso; Christoph Seiler; Marni J Falk
Journal:  Neurochem Int       Date:  2017-07-18       Impact factor: 3.921

Review 3.  Neurodevelopmental manifestations of mitochondrial disease.

Authors:  Marni J Falk
Journal:  J Dev Behav Pediatr       Date:  2010-09       Impact factor: 2.225

Review 4.  OXPHOS mutations and neurodegeneration.

Authors:  Werner J H Koopman; Felix Distelmaier; Jan A M Smeitink; Peter H G M Willems
Journal:  EMBO J       Date:  2012-11-13       Impact factor: 11.598

Review 5.  Engineering the alternative oxidase gene to better understand and counteract mitochondrial defects: state of the art and perspectives.

Authors:  Riyad El-Khoury; Kia K Kemppainen; Eric Dufour; Marten Szibor; Howard T Jacobs; Pierre Rustin
Journal:  Br J Pharmacol       Date:  2014-04       Impact factor: 8.739

6.  Hyperactivation of oxidative mitochondrial metabolism in epithelial cancer cells in situ: visualizing the therapeutic effects of metformin in tumor tissue.

Authors:  Diana Whitaker-Menezes; Ubaldo E Martinez-Outschoorn; Neal Flomenberg; Ruth C Birbe; Agnieszka K Witkiewicz; Anthony Howell; Stephanos Pavlides; Aristotelis Tsirigos; Adam Ertel; Richard G Pestell; Paolo Broda; Carlo Minetti; Michael P Lisanti; Federica Sotgia
Journal:  Cell Cycle       Date:  2011-12-01       Impact factor: 4.534

Review 7.  Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.

Authors:  Patrick Yu-Wai-Man; Philip G Griffiths; Patrick F Chinnery
Journal:  Prog Retin Eye Res       Date:  2010-11-26       Impact factor: 21.198

8.  PARP inhibition delays progression of mitochondrial encephalopathy in mice.

Authors:  Roberta Felici; Leonardo Cavone; Andrea Lapucci; Daniele Guasti; Daniele Bani; Alberto Chiarugi
Journal:  Neurotherapeutics       Date:  2014-07       Impact factor: 7.620

9.  Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.

Authors:  Mathieu Marella; Byoung Boo Seo; Biju B Thomas; Akemi Matsuno-Yagi; Takao Yagi
Journal:  PLoS One       Date:  2010-07-08       Impact factor: 3.240

10.  Mitochondrial Dysfunction and Chronic Disease: Treatment With Natural Supplements.

Authors:  Garth L Nicolson
Journal:  Integr Med (Encinitas)       Date:  2014-08
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.