Literature DB >> 23347562

Wnt signaling in stem and cancer stem cells.

Jane D Holland1, Alexandra Klaus, Alistair N Garratt, Walter Birchmeier.   

Abstract

The functional versatility of Wnt/β-catenin signaling can be seen by its ability to act in stem cells of the embryo and of the adult as well as in cancer stem cells. During embryogenesis, stem cells demonstrate a requirement for β-catenin in mediating the response to Wnt signaling for their maintenance and transition from a pluripotent state. In adult stem cells, Wnt signaling functions at various hierarchical levels to contribute to specification of different tissues. This has raised the possibility that the tightly regulated self-renewal mediated by Wnt signaling in stem and progenitor cells is subverted in cancer cells to allow malignant progression. Intensive work is currently being performed to resolve how intrinsic and extrinsic factors that regulate Wnt/β-catenin signaling coordinate the stem and cancer stem cell states.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23347562     DOI: 10.1016/j.ceb.2013.01.004

Source DB:  PubMed          Journal:  Curr Opin Cell Biol        ISSN: 0955-0674            Impact factor:   8.382


  214 in total

Review 1.  Regulation of Wnt signaling by protocadherins.

Authors:  Kar Men Mah; Joshua A Weiner
Journal:  Semin Cell Dev Biol       Date:  2017-08-01       Impact factor: 7.727

2.  The C. elegans embryonic fate specification factor EGL-18 (GATA) is reutilized downstream of Wnt signaling to maintain a population of larval progenitor cells.

Authors:  Lakshmi Gorrepati; David M Eisenmann
Journal:  Worm       Date:  2015-01-27

3.  Hypothalamic radial glia function as self-renewing neural progenitors in the absence of Wnt/β-catenin signaling.

Authors:  Robert N Duncan; Yuanyuan Xie; Adam D McPherson; Andrew V Taibi; Joshua L Bonkowsky; Adam D Douglass; Richard I Dorsky
Journal:  Development       Date:  2015-11-24       Impact factor: 6.868

4.  Enhanced Wnt signaling by methylation-mediated loss of SFRP2 promotes osteosarcoma cell invasion.

Authors:  Qiang Xiao; Yu Yang; Xuepu Zhang; Qing An
Journal:  Tumour Biol       Date:  2015-12-01

5.  The tumor suppressor LKB1 antagonizes WNT signaling pathway through modulating GSK3β activity in cell growth of esophageal carcinoma.

Authors:  Kai Liu; Yue Luo; Hui Tian; Kai-Zhong Yu; Jin-Xian He; Wei-Yu Shen
Journal:  Tumour Biol       Date:  2014-02

6.  Destabilization of heterologous proteins mediated by the GSK3β phosphorylation domain of the β-catenin protein.

Authors:  Yuhan Kong; Hongyu Zhang; Xian Chen; Wenwen Zhang; Chen Zhao; Ning Wang; Ningning Wu; Yunfeng He; Guoxin Nan; Hongmei Zhang; Sheng Wen; Fang Deng; Zhan Liao; Di Wu; Junhui Zhang; Xinyue Qin; Rex C Haydon; Hue H Luu; Tong-Chuan He; Lan Zhou
Journal:  Cell Physiol Biochem       Date:  2013-11-14

Review 7.  Intestinal stem cells and the colorectal cancer microenvironment.

Authors:  Bryan A Ong; Kenneth J Vega; Courtney W Houchen
Journal:  World J Gastroenterol       Date:  2014-02-28       Impact factor: 5.742

8.  An investigation of the effects of the core protein telomerase reverse transcriptase on Wnt signaling in breast cancer cells.

Authors:  Imke Listerman; Francesca S Gazzaniga; Elizabeth H Blackburn
Journal:  Mol Cell Biol       Date:  2013-11-11       Impact factor: 4.272

9.  Transforming growth factor-β1 (TGF-β1) induces mouse precartilaginous stem cell differentiation through TGFRII-CK1ε-β-catenin signalling.

Authors:  Wang Qiong; Gu Xiaofeng; Wang Junfang
Journal:  Int J Exp Pathol       Date:  2018-08-02       Impact factor: 1.925

10.  Testing models of the APC tumor suppressor/β-catenin interaction reshapes our view of the destruction complex in Wnt signaling.

Authors:  Robert J Yamulla; Eric G Kane; Alexandra E Moody; Kristin A Politi; Nicole E Lock; Andrew V A Foley; David M Roberts
Journal:  Genetics       Date:  2014-06-14       Impact factor: 4.562

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