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MicroRNA Regulation of Cholesterol Metabolism

机译:胆固醇代谢的MicroRNA调控

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Disruption of cellular cholesterol balance results in pathologic processes including atherosclerosis, metabolic syndrome, type II diabetes and Alzheimer's disease. Maintenance of cholesterol homeostasis requires constant metabolic adjustment, achieved partly through the fine regulation of the classical transcription factors (e.g., by SREBP and LXR), but also through members of a class of noncoding RNAs termed miRNAs. Some miRNAs have now been identified to be potent post-transcriptional regulators of lipid metabolism genes, including miR-122, miR-33, miR-758, and miR-106b. Different strategies have been developed to modulate miRNA effects for therapeutic purposes. The promise demonstrated by the use of anti-miRs in human preclinical studies, in the case of miR-122, raises the possibility that miR-33, miR-758, and miR-106b may become viable therapeutic targets in future. This review summarizes the evidence for a critical role of some miRNAs in regulating cholesterol metabolism and suggests novel ways to manage dyslipidemias and cardiovascular diseases.
机译:细胞胆固醇平衡的破坏导致包括动脉粥样硬化,代谢综合征,II型糖尿病和阿尔茨海默氏病的病理过程。维持胆固醇稳态需要不断的代谢调节,这部分通过经典转录因子的精细调节(例如通过SREBP和LXR)来实现,但也可以通过一类称为miRNA的非编码RNA的成员来实现。现已鉴定出一些miRNA是脂质代谢基因的有效转录后调节剂,包括miR-122,miR-33,miR-758和miR-106b。为了治疗目的,已经开发出不同的策略来调节miRNA作用。在人类临床前研究中使用抗miRs所显示的希望,就miR-122而言,增加了miR-33,miR-758和miR-106b将来可能成为可行的治疗靶标的可能性。这篇综述总结了一些miRNA在调节胆固醇代谢中的关键作用的证据,并提出了治疗血脂异常和心血管疾病的新方法。

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