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Wnt/beta-catenin signaling: components, mechanisms, and diseases.

作者信息

MacDonald Bryan T, Tamai Keiko, He Xi

机构信息

F. M. Kirby Neurobiology Center, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Dev Cell. 2009 Jul;17(1):9-26. doi: 10.1016/j.devcel.2009.06.016.


DOI:10.1016/j.devcel.2009.06.016
PMID:19619488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2861485/
Abstract

Signaling by the Wnt family of secreted glycolipoproteins via the transcriptional coactivator beta-catenin controls embryonic development and adult homeostasis. Here we review recent progress in this so-called canonical Wnt signaling pathway. We discuss Wnt ligands, agonists, and antagonists, and their interactions with Wnt receptors. We also dissect critical events that regulate beta-catenin stability, from Wnt receptors to the cytoplasmic beta-catenin destruction complex, and nuclear machinery that mediates beta-catenin-dependent transcription. Finally, we highlight some key aspects of Wnt/beta-catenin signaling in human diseases including congenital malformations, cancer, and osteoporosis, and discuss potential therapeutic implications.

摘要

相似文献

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本文引用的文献

[1]
The tortoise and the hair: slow-cycling cells in the stem cell race.

Cell. 2009-5-29

[2]
The vertebrate primary cilium in development, homeostasis, and disease.

Cell. 2009-4-3

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Cell. 2009-3-20

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PLoS One. 2009

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Nat Chem Biol. 2009-4

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Nat Chem Biol. 2009-2

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