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本文引用的文献

1
Flavin-containing monooxygenase 3 as a potential player in diabetes-associated atherosclerosis.含黄素单加氧酶3作为糖尿病相关动脉粥样硬化的潜在参与者。
Nat Commun. 2015 Apr 7;6:6498. doi: 10.1038/ncomms7498.
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MicroRNA-223 coordinates cholesterol homeostasis.微小RNA-223协调胆固醇稳态。
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Regulation of microRNA biogenesis.miRNA 生物发生的调控。
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HDL and cholesterol handling in the brain.高密度脂蛋白和胆固醇在大脑中的转运。
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Inhibition of microRNA-24 expression in liver prevents hepatic lipid accumulation and hyperlipidemia.抑制肝脏中 microRNA-24 的表达可预防肝内脂质堆积和高脂血症。
Hepatology. 2014 Aug;60(2):554-64. doi: 10.1002/hep.27153. Epub 2014 May 19.
6
Identification of miR-185 as a regulator of de novo cholesterol biosynthesis and low density lipoprotein uptake.鉴定 miR-185 作为从头胆固醇生物合成和低密度脂蛋白摄取的调节剂。
J Lipid Res. 2014 Feb;55(2):226-38. doi: 10.1194/jlr.M041335. Epub 2013 Dec 2.
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Pharmacological inhibition of a microRNA family in nonhuman primates by a seed-targeting 8-mer antimiR.通过一种靶向种子的 8 个碱基的反 miRNA 抑制非人灵长类动物中的 microRNA 家族。
Sci Transl Med. 2013 Nov 20;5(212):212ra162. doi: 10.1126/scitranslmed.3006840.
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The role of signalling in cellular cholesterol homeostasis.信号在细胞胆固醇稳态中的作用。
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9
An SREBP-responsive microRNA operon contributes to a regulatory loop for intracellular lipid homeostasis.一个受 SREBP 响应的 microRNA 操纵子有助于细胞内脂质稳态的调控回路。
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10
MicroRNA-144 regulates hepatic ATP binding cassette transporter A1 and plasma high-density lipoprotein after activation of the nuclear receptor farnesoid X receptor.微小 RNA-144 调节核受体法尼醇 X 受体激活后的肝 ATP 结合盒转运蛋白 A1 和血浆高密度脂蛋白。
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微小RNA与胆固醇稳态

miRNA and cholesterol homeostasis.

作者信息

Jeon Tae-Il, Osborne Timothy F

机构信息

Department of Animal Science, Chonnam National University, Gwangju 61186, South Korea.

Integrative Metabolism Program, Sanford.Burnham.Prebys Medical Discovery Institute, Orlando, FL, United States.

出版信息

Biochim Biophys Acta. 2016 Dec;1861(12 Pt B):2041-2046. doi: 10.1016/j.bbalip.2016.01.005. Epub 2016 Jan 15.

DOI:10.1016/j.bbalip.2016.01.005
PMID:26778752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4980302/
Abstract

MicroRNAs (miRNAs) have recently emerged as a novel class of epigenetic regulators of gene expression. They are systemically involved in the control of lipid metabolism through a complex interactive mechanism that involves gene regulatory networks. Hence, they can contribute to defective lipid metabolism and metabolic diseases. Here, we review recent advances in the roles of lipid-sensing transcription factors in regulating miRNA gene networks, as well as miRNA expression and function in the regulation of cholesterol metabolism. This article is part of a Special Issue entitled: MicroRNAs and lipid/energy metabolism and related diseases edited by Carlos Fernández-Hernando and Yajaira Suárez.

摘要

微小RNA(miRNA)最近作为一类新型的基因表达表观遗传调节因子出现。它们通过涉及基因调控网络的复杂相互作用机制,系统性地参与脂质代谢的控制。因此,它们可能导致脂质代谢缺陷和代谢性疾病。在这里,我们综述了脂质感应转录因子在调节miRNA基因网络中的作用,以及miRNA在胆固醇代谢调节中的表达和功能方面的最新进展。本文是由卡洛斯·费尔南德斯 - 埃尔南多和亚贾伊拉·苏亚雷斯编辑的名为《微小RNA与脂质/能量代谢及相关疾病》特刊的一部分。