miR-33a/b contribute to the regulation of fatty acid metabolism and insulin signaling

New York University · Kettering University · +6 more institutions

PubMed
Indexed incrossrefpubmed

Abstract

Cellular imbalances of cholesterol and fatty acid metabolism result in pathological processes, including atherosclerosis and metabolic syndrome. Recent work from our group and others has shown that the intronic microRNAs hsa-miR-33a and hsa-miR-33b are located within the sterol regulatory element-binding protein-2 and -1 genes, respectively, and regulate cholesterol homeostasis in concert with their host genes. Here, we show that miR-33a and -b also regulate genes involved in fatty acid metabolism and insulin signaling. miR-33a and -b target key enzymes involved in the regulation of fatty acid oxidation, including carnitine O-octaniltransferase, carnitine palmitoyltransferase 1A, hydroxyacyl-CoA-dehydrogenase,…

Citation impact

658
total citations
FWCI
22.49
Percentile
100%
References
38
Citations per year

Authors

17

Topics & keywords

Keywords
  • Insulin receptor
  • Sterol regulatory element-binding protein
  • Endocrinology
  • Biology
  • Internal medicine
  • Fatty acid metabolism
  • Insulin
  • Insulin receptor substrate
UN Sustainable Development Goals
  • Good health and well-being
No related works found for this paper.

Funding