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Repairing Mitochondrial Dysfunction in Disease
Vincenzo Sorrentino, Keir J. Menzies, Johan Auwerx
The Annual Review of Pharmacology and Toxicology · 2017 · ▲ 345 citations
Abstract
Mitochondria are essential organelles for many aspects of cellular homeostasis, including energy harvesting through oxidative phosphorylation. Alterations of mitochondrial function not only impact on cellular metabolism but also critically influence whole-body metabolism, health, and life span. Diseases defined by mitochondrial dysfunction(definition) have expanded from rare monogenic disorders in a strict sense to now also include many common polygenic diseases, including metabolic, cardiovascular, neurodegenerative, and neuromuscular diseases. This has led to an intensive search for new therapeutic and preventive strategies aimed at invigorating mitochondrial function by exploiting key components of mitochondrial biogenesis, redox metabolism, dynamics, mitophagy, and the mitochondrial unfolded protein response. As such, new findings linking mitochondrial function to the progression or outcome of this ever-increasing list of diseases has stimulated the discovery and development of the first true mitochondrial drugs, which are now entering the clinic and are discussed in this review.
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- DOI
- 10.1146/annurev-pharmtox-010716-104908
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- 2026-07-24 MST
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APA
Sorrentino, V., Menzies, K.J., & Auwerx, J. (2017). Repairing Mitochondrial Dysfunction in Disease. <em>The Annual Review of Pharmacology and Toxicology</em>. https://doi.org/10.1146/annurev-pharmtox-010716-104908
Vancouver
Sorrentino V, Menzies KJ, Auwerx J. Repairing Mitochondrial Dysfunction in Disease. The Annual Review of Pharmacology and Toxicology. 2017. doi:10.1146/annurev-pharmtox-010716-104908.
BibTeX
@unpublished{vincenzo2017Repair,
title = {Repairing Mitochondrial Dysfunction in Disease},
author = {Vincenzo Sorrentino and Keir J. Menzies and Johan Auwerx},
journal = {The Annual Review of Pharmacology and Toxicology},
year = {2017},
doi = {10.1146/annurev-pharmtox-010716-104908},
}
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