Use of miRNA-483 and its Target Genes in Treatment of Cardiovascular and Inflammatory Diseases

Application

Therapeutic use of miR-483 mimic for treating aortic valve clarification.

Key Benefits

  • MiR-483 or mimics of miR-483 could be used as a therapeutic.
  • Could also be a target for additional drug development toward a non-invasive therapy for aortic valve calcification.

Market Summary

Aortic stenosis (AS) is the most common type of heart valve disease in the elderly, affecting 4.6% of people over the age of 75. AS is often caused by aortic valve calcification (AVC), a degenerative disease of the heart that causes narrowing of the aortic valve. As the population ages, AS and AVC become increasingly important public health problems. There is a need for a non-surgical, therapeutic approach to treat aortic valve calcification.

Technical Summary

Aortic stenosis limits the amount of blood that can leave the valve and thus causes the heart to pump blood through the valve at an increased force, this is mainly caused by narrowing due to aortic valve calcification. Aortic valve calcification calcium deposits form on the aortic valve in the heart. Said deposits can cause narrowing at the opening of the aortic valve which can require valve repair surgery. Researchers at Emory have discovered that a differentially expressed, flow sensitive, microRNA (miRNAs) in the aorta and heat takes part in controlling inflammation and progressive calcification of the aortic valve. Using human endothelial cell lines, the researchers demonstrated that expression of miR-483 decreased under conditions of oscillatory flow. Furthermore, work was done to validate that ubiquitin E2 ligase expression is regulated by miR-483 which in regulates inflammation via degrading von-Hippel-Lindau tumor suppressor protein and then increasing expression of HIF1α thus leading to inflammation and progressive calcification.

Developmental Stage

Animal testing conducted.

Publications

BMES Meeting, 10/12/2017
Fernandez-Esmerats J, et al Arterioscler Thromb Vasc Biol. 2019;39(3):467-481. PMC6393167

Patent Information

App Type Country Serial No. Patent No. File Date Issued Date Patent Status
Utility (parent) United States 16/156,917 11,225,660 10/10/2018 1/18/2022 Issued
Divisional United States 17/544,801 11,976,279 12/7/2021 5/7/2024 Issued
Tech ID: 18014
Published: 7/6/2022