Literature DB >> 20829110

Molecular biology and functional genomics of liver X receptors (LXR) in relationship to metabolic diseases.

Malin Hedengran Faulds1, Chunyan Zhao, Karin Dahlman-Wright.   

Abstract

The metabolic syndrome constitutes a group of metabolic conditions that increase the risk of developing diseases, including cardiovascular disease (CVD) and type 2 diabetes (T2D). LXRα/β are regulators of lipogenesis, cholesterol/glucose homoeostasis and inflammatory pathways, processes that are intertwined with development of the metabolic syndrome. The employment of LXRs as pharmaceutical targets for treatment of various aspects of the metabolic syndrome has been promptly investigated but serious side effects, like hepatic steatosis, have hampered this process. Novel treatment regimes now focus on development of isoform-specific or tissue-specific LXR agonist/antagonist compounds to circumvent effects on lipid biosynthesis. Other strategies to explore the beneficial aspects of LXR activation include targeting co-factors or pathways that are modifying LXR activity.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20829110     DOI: 10.1016/j.coph.2010.07.003

Source DB:  PubMed          Journal:  Curr Opin Pharmacol        ISSN: 1471-4892            Impact factor:   5.547


  20 in total

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3.  Nogo-B receptor deficiency increases liver X receptor alpha nuclear translocation and hepatic lipogenesis through an adenosine monophosphate-activated protein kinase alpha-dependent pathway.

Authors:  Wenquan Hu; Wenwen Zhang; Yuanli Chen; Ujala Rana; Ru-Jeng Teng; Yajun Duan; Zhong Liu; Baofeng Zhao; Jamie Foeckler; Hartmut Weiler; Rachel E Kallinger; Michael J Thomas; Kezhong Zhang; Jihong Han; Qing Robert Miao
Journal:  Hepatology       Date:  2016-08-23       Impact factor: 17.425

4.  MiR-106b impairs cholesterol efflux and increases Aβ levels by repressing ABCA1 expression.

Authors:  Jaekwang Kim; Hyejin Yoon; Cristina M Ramírez; Sang-Mi Lee; Hyang-Sook Hoe; Carlos Fernández-Hernando; Jungsu Kim
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5.  Endothelial cellular senescence is inhibited by liver X receptor activation with an additional mechanism for its atheroprotection in diabetes.

Authors:  Toshio Hayashi; Hitoshi Kotani; Tomoe Yamaguchi; Kumiko Taguchi; Mayu Iida; Koichiro Ina; Morihiko Maeda; Masafumi Kuzuya; Yuichi Hattori; Louis J Ignarro
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-07       Impact factor: 11.205

6.  Activation of liver-X-receptor α but not liver-X-receptor β protects against myocardial ischemia/reperfusion injury.

Authors:  Qing He; Jun Pu; Ancai Yuan; Wayne Bond Lau; Erhe Gao; Walter J Koch; Xin-Liang Ma; Ben He
Journal:  Circ Heart Fail       Date:  2014-10-02       Impact factor: 8.790

7.  Aberrant activation of liver X receptors impairs pancreatic beta cell function through upregulation of sterol regulatory element-binding protein 1c in mouse islets and rodent cell lines.

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8.  Liver X receptor modulates diabetic retinopathy outcome in a mouse model of streptozotocin-induced diabetes.

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Journal:  AAPS J       Date:  2012-11-22       Impact factor: 4.009

10.  Lack of liver X receptors leads to cell proliferation in a model of mouse dorsal prostate epithelial cell.

Authors:  Julie Dufour; Aurélien Pommier; Georges Alves; Hugues De Boussac; Corinne Lours-Calet; David H Volle; Jean-Marc A Lobaccaro; Silvère Baron
Journal:  PLoS One       Date:  2013-03-12       Impact factor: 3.240

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