MicroRNA调控胆固醇代谢。

Cholesterol Pub Date : 2012-01-01 DOI:10.1155/2012/847849
Noemi Rotllan, Carlos Fernández-Hernando
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引用次数: 78

摘要

细胞胆固醇平衡的破坏导致病理过程,包括动脉粥样硬化、代谢综合征、II型糖尿病和阿尔茨海默病。维持胆固醇稳态需要持续的代谢调节,部分通过经典转录因子(如SREBP和LXR)的精细调节来实现,但也通过一类被称为mirna的非编码rna的成员来实现。一些mirna现已被鉴定为脂质代谢基因的有效转录后调节因子,包括miR-122、miR-33、miR-758和miR-106b。为了达到治疗目的,已经开发了不同的策略来调节miRNA的作用。以miR-122为例,抗mir在人类临床前研究中的应用前景表明,miR-33、miR-758和miR-106b在未来可能成为可行的治疗靶点。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,并提出了控制血脂异常和心血管疾病的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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MicroRNA Regulation of Cholesterol Metabolism.

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.

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