» Articles » PMID: 30227643

Regulation of Sphingolipid Metabolism by MicroRNAs: A Potential Approach to Alleviate Atherosclerosis

Overview
Journal Diseases
Date 2018 Sep 20
PMID 30227643
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

The rapidly expanding field of bioactive lipids is exemplified by the many sphingolipids, which are structurally and functionally diverse molecules with significant physiologic functions. These sphingolipids are main constituents of cellular membranes and have been found associated with plasma lipoproteins, and their concentrations are altered in several metabolic disorders such as atherosclerosis, obesity, and diabetes. Understanding the mechanisms that regulate their biosynthesis and secretion may provide novel information that might be amenable to therapeutic targeting in the treatment of these diseases. Several sphingolipid synthesis genes have been targeted as potential therapeutics for atherosclerosis. In recent years, significant progress has been made in studying the role of microRNAs (miRNAs) in lipid metabolism. However, little effort has been made to investigate their role in sphingolipid metabolism. Sphingolipid biosynthetic pathways involve various enzymes that lead to the formation of several key molecules implicated in atherosclerosis, and the identification of miRNAs that regulate these enzymes could help us to understand these complex pathways better and may prove beneficial in alleviating atherosclerosis.

Citing Articles

The Acid Sphingomyelinase Inhibitor Amitriptyline Ameliorates TNF-α-Induced Endothelial Dysfunction.

Ji Y, Chen J, Pang L, Chen C, Ye J, Liu H Cardiovasc Drugs Ther. 2022; 38(1):43-56.

PMID: 36103099 PMC: 10876840. DOI: 10.1007/s10557-022-07378-0.


LncRNA MALAT1 Suppression Protects Endothelium against oxLDL-Induced Inflammation via Inhibiting Expression of MiR-181b Target Gene TOX.

Wang L, Qi Y, Wang Y, Tang H, Li Z, Wang Y Oxid Med Cell Longev. 2020; 2019:8245810.

PMID: 31949884 PMC: 6942911. DOI: 10.1155/2019/8245810.


Ceramide and Sphingosine Regulation of Myelinogenesis: Targeting Serine Palmitoyltransferase Using microRNA in Multiple Sclerosis.

Dasgupta S, Ray S Int J Mol Sci. 2019; 20(20).

PMID: 31614447 PMC: 6834223. DOI: 10.3390/ijms20205031.

References
1.
Park T, Panek R, Mueller S, Hanselman J, Rosebury W, Robertson A . Inhibition of sphingomyelin synthesis reduces atherogenesis in apolipoprotein E-knockout mice. Circulation. 2004; 110(22):3465-71. DOI: 10.1161/01.CIR.0000148370.60535.22. View

2.
Li Z, Fan Y, Liu J, Li Y, Huan C, Bui H . Impact of sphingomyelin synthase 1 deficiency on sphingolipid metabolism and atherosclerosis in mice. Arterioscler Thromb Vasc Biol. 2012; 32(7):1577-84. PMC: 3444302. DOI: 10.1161/ATVBAHA.112.251538. View

3.
Rayner K, Suarez Y, Davalos A, Parathath S, Fitzgerald M, Tamehiro N . MiR-33 contributes to the regulation of cholesterol homeostasis. Science. 2010; 328(5985):1570-3. PMC: 3114628. DOI: 10.1126/science.1189862. View

4.
Scholer N, Langer C, Dohner H, Buske C, Kuchenbauer F . Serum microRNAs as a novel class of biomarkers: a comprehensive review of the literature. Exp Hematol. 2010; 38(12):1126-30. DOI: 10.1016/j.exphem.2010.10.004. View

5.
Lallemand T, Rouahi M, Swiader A, Grazide M, Geoffre N, Alayrac P . nSMase2 (Type 2-Neutral Sphingomyelinase) Deficiency or Inhibition by GW4869 Reduces Inflammation and Atherosclerosis in Apoe Mice. Arterioscler Thromb Vasc Biol. 2018; 38(7):1479-1492. PMC: 6039418. DOI: 10.1161/ATVBAHA.118.311208. View