4.6 Review

Targeting mitochondria for cardiovascular disorders: therapeutic potential and obstacles

Journal

NATURE REVIEWS CARDIOLOGY
Volume 16, Issue 1, Pages 33-55

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41569-018-0074-0

Keywords

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Funding

  1. Polish National Science Centre [UMO-2014/15/B/NZ1/00490]
  2. Glenn Foundation for Medical Research
  3. Sinclair Gift Fund
  4. US NIH/National Institute on Aging [R01 AG028730, R01 DK100263]
  5. Ligue Nationale contre le Cancer Comite de Charente-Maritime (equipe labellisee)
  6. Agence National de la Recherche (ANR) - Projets blancs
  7. ANR
  8. ERA-Net for Research on Rare Diseases
  9. Association pour la recherche sur le cancer (ARC)
  10. Canceropole Ile-de-France
  11. Fondation pour la Recherche Medicale (FRM)
  12. European Commission (ArtForce)
  13. European Research Council (ERC)
  14. Fondation Carrefour
  15. Institut National du Cancer (INCa)
  16. INSERM (HTE)
  17. Institut Universitaire de France
  18. LeDucq Foundation
  19. LabEx Immuno-Oncology
  20. Seerave Foundation
  21. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  22. SIRIC Cancer Research and Personalized Medicine (CARPEM)
  23. Paris Alliance of Cancer Research Institutes (PACRI)
  24. Italian Ministry of Education, the University and Research
  25. Telethon [GGP15219/B]
  26. Italian Association for Cancer Research (AIRC) [IG-18624]
  27. University of Ferrara (Ferrara, Italy)
  28. Department of Radiation Oncology at Weill Cornell Medicine (New York, NY, USA)
  29. Chancelerie des universites de Paris (Legs Poix)
  30. RHU Torino Lumiere
  31. NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH [R21DE027490] Funding Source: NIH RePORTER
  32. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK100263] Funding Source: NIH RePORTER
  33. NATIONAL INSTITUTE ON AGING [R01AG019719, DP1AG058605, R37AG028730] Funding Source: NIH RePORTER

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A large body of evidence indicates that mitochondrial dysfunction has a major role in the pathogenesis of multiple cardiovascular disorders. Over the past 2 decades, extraordinary efforts have been focused on the development of agents that specifically target mitochondria for the treatment of cardiovascular disease. Despite such an intensive wave of investigation, no drugs specifically conceived to modulate mitochondrial functions are currently available for the clinical management of cardiovascular disease. In this Review, we discuss the therapeutic potential of targeting mitochondria in patients with cardiovascular disease, examine the obstacles that have restrained the development of mitochondria-targeting agents thus far, and identify strategies that might empower the full clinical potential of this approach.

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