DES1: A Key Driver of Lipotoxicity in Metabolic Disease
Author(s) -
Jeremy T. Blitzer,
Liping Wang,
Scott A. Summers
Publication year - 2020
Publication title -
dna and cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.895
H-Index - 77
eISSN - 1557-7430
pISSN - 1044-5498
DOI - 10.1089/dna.2020.5402
Subject(s) - ceramide , lipotoxicity , biology , disease , nonalcoholic fatty liver disease , sphingolipid , diabetes mellitus , metabolic disease , lipid metabolism , cardiomyopathy , diabetic cardiomyopathy , bioinformatics , endocrinology , medicine , insulin resistance , fatty liver , biochemistry , heart failure , apoptosis
Ceramides have emerged as important regulators of tissue metabolism that play essential roles in cardiometabolic disease. They are potent biomarkers of diabetes and heart disease and are now being measured clinically as predictors of major adverse cardiac events. Moreover, studies in rodents reveal that inhibitors of ceramide synthesis prevent or reverse the pathogenic features of type 2 diabetes, nonalcoholic fatty liver disease, atherosclerosis, and cardiomyopathy. Herein the authors discuss inhibition of dihydroceramide desaturase-1, the final enzyme in the ceramide biosynthesis pathway, as a potential therapeutic approach to lower ceramides and combat cardiometabolic disease.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom