MicroRNAs in obesity-associated disorders

被引:50
作者
Abente, Eugenio J. [1 ,2 ]
Subramanian, Murugan [1 ,2 ]
Ramachandran, Vimal [1 ,2 ]
Najafi-Shoushtari, S. Hani [1 ,2 ]
机构
[1] Cornell Univ, Weill Cornell Med Coll, Dept Cell & Dev Biol, New York, NY 10021 USA
[2] Qatar Fdn, Weill Cornell Med Coll Qatar, Doha, Qatar
关键词
Obesity; MicroRNAs; Lipid/fat metabolism; Metabolic syndrome; Insulin resistance; RNA therapeutics; STEROL REGULATORY ELEMENT; PREGNANE-X-RECEPTOR; HEPATIC LIPID-ACCUMULATION; ADIPOSE-TISSUE DYSFUNCTION; LEUCINE ZIPPER PROTEIN; ADIPOCYTE DIFFERENTIATION; INSULIN-RESISTANCE; BILE-ACID; POSTTRANSCRIPTIONAL REGULATION; CHOLESTEROL-METABOLISM;
D O I
10.1016/j.abb.2015.09.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The emergence of a worldwide obesity epidemic has dramatically increased the prevalence of insulin resistance and metabolic syndrome, predisposing individuals to a greater risk for the development of non-alcoholic fatty liver disease, type II diabetes and atherosclerotic cardiovascular diseases. Current available pharmacological interventions combined with diet and exercise-based managements are still poorly effective for weight management, likely in part due to an incomplete understanding of regulatory mechanisms and pathways contributing to the systemic metabolic abnormalities under disturbed energy homeostasis. MicroRNAs, small non-coding RNAs that regulate posttranscriptional gene expression, have been increasingly described to influence shifts in metabolic pathways under various obesity-related disease settings. Here we review recent discoveries of the mechanistic role that microRNAs play in regulating metabolic functions in liver and adipose tissues involved in obesity associated disorders, and briefly discusses the potential candidates that are being pursued as viable therapeutic targets. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:108 / 119
页数:12
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