Application of microRNAs in diabetes mellitus
- 1Li Ka Sing Faculty of Medicine, School of Chinese Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong
2Department of Medicine and Therapeutics, Faculty of Medicine, Li Ka Shing Institute of Health Science, The Chinese University of Hong Kong, Shatin, Hong Kong
3Centre for Biosystems and Genome Network Medicine, Ioannina University, Ioannina, Greece
4Department of Clinical Oncology, Queen Elizabeth Hospital, Kowloon, Hong Kong
- Correspondence should be addressed to W C Cho; Email: williamcscho{at}gmail.com
Abstract
MicroRNAs (miRNAs) are small molecules negatively regulating gene expression by diminishing their target mRNAs. Emerging studies have shown that miRNAs play diverse roles in diabetes mellitus. Type 1 diabetes (T1D) and T2D are two major types of diabetes. T1D is characterized by a reduction in insulin release from the pancreatic β-cells, while T2D is caused by islet β-cell dysfunction in response to insulin resistance. This review describes the miRNAs that control insulin release and production by regulating cellular membrane electrical excitability (ATP:ADP ratio), insulin granule exocytosis, insulin synthesis in β-cells, and β-cell fate and islet mass formation. This review also examines miRNAs involved the insulin resistance of liver, fat, and skeletal muscle, which change insulin sensitivity pathways (insulin receptors, glucose transporter type 4, and protein kinase B pathways). This review discusses the potential application of miRNAs in diabetes, including the use of gene therapy and therapeutic compounds to recover miRNA function in diabetes, as well as the role of miRNAs as potential biomarkers for T1D and T2D.
- Received in final form 31 March 2014
- Accepted 24 April 2014
- Made available online as an Accepted Preprint 29 April 2014
- © 2014 Society for Endocrinology