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LRP5 和 LRP6 在发育和疾病中的作用。

LRP5 and LRP6 in development and disease.

机构信息

Center for Skeletal Disease Research, Laboratory of Cell Signaling and Carcinogenesis, Van Andel Research Institute, Grand Rapids, MI 49503, USA.

出版信息

Trends Endocrinol Metab. 2013 Jan;24(1):31-9. doi: 10.1016/j.tem.2012.10.003.


DOI:10.1016/j.tem.2012.10.003
PMID:23245947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3592934/
Abstract

Low-density lipoprotein-related receptors 5 and 6 (LRP5/6) are highly homologous proteins with key functions in canonical Wnt signaling. Alterations in the genes encoding these receptors or their interacting proteins are linked to human diseases, and as such they have been a major focus of drug development efforts to treat several human conditions including osteoporosis, cancer, and metabolic disease. Here, we discuss the links between alterations in LRP5/6 and disease, proteins that interact with them, and insights gained into their function from mouse models. We also highlight current drug development related to LRP5/6 as well as how the recent elucidation of their crystal structures may allow further refinement of our ability to target them for therapeutic benefit.

摘要

低密度脂蛋白相关受体 5 和 6(LRP5/6)是高度同源的蛋白质,在经典 Wnt 信号通路中具有关键作用。编码这些受体或其相互作用蛋白的基因突变与人类疾病有关,因此它们一直是药物开发的重点,旨在治疗多种人类疾病,包括骨质疏松症、癌症和代谢疾病。在这里,我们讨论了 LRP5/6 的改变与疾病、与它们相互作用的蛋白质之间的联系,以及从小鼠模型中获得的对它们功能的深入了解。我们还强调了与 LRP5/6 相关的当前药物开发,以及最近对其晶体结构的阐明如何使我们进一步提高靶向治疗的能力。

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[3]
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[5]
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[6]
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本文引用的文献

[1]
Characterization of the interaction of sclerostin with the low density lipoprotein receptor-related protein (LRP) family of Wnt co-receptors.

J Biol Chem. 2012-6-13

[2]
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Cell. 2012-6-8

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Cell. 2012-6-8

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Structural basis of Wnt recognition by Frizzled.

Science. 2012-5-31

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Nature. 2012-4-29

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The R-spondin protein family.

Genome Biol. 2012

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Modulation of β-catenin signaling by glucagon receptor activation.

PLoS One. 2012-3-16

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LRP6 protein regulates low density lipoprotein (LDL) receptor-mediated LDL uptake.

J Biol Chem. 2011-11-28

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Calcific aortic valve disease: not simply a degenerative process: A review and agenda for research from the National Heart and Lung and Blood Institute Aortic Stenosis Working Group. Executive summary: Calcific aortic valve disease-2011 update.

Circulation. 2011-10-18

[10]
Structural basis of Wnt signaling inhibition by Dickkopf binding to LRP5/6.

Dev Cell. 2011-10-13

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