Literature DB >> 9097727

WNTs modulate cell fate and behavior during vertebrate development.

R T Moon1, J D Brown, M Torres.   

Abstract

Wnt genes encode a family of secreted glycoproteins that modulate cell fate and behavior in embryos through activation of receptor-mediated signaling pathways. Wnt sequences, patterns of expression and activities are highly conserved in evolution, so it has been possible to gain insights into the functions, and mechanisms of action, of the Wnt genes through a synthesis of genetic and cell biological approaches in different organisms. These studies suggest that there are functionally distinct WNT proteins as assayed by the ability to transform cells and by differences in embryonic responses to ectopic WNT signals. Moreover, gain-of-function and loss-of-function studies both support the involvement of Wnt proteins in modulating cell fate and cell behavior during vertebrate development, often through combinatorial interactions with other signaling pathways to regulate gene expression.

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Year:  1997        PMID: 9097727     DOI: 10.1016/s0168-9525(97)01093-7

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  127 in total

1.  Axis determination by inhibition of Wnt signaling in Xenopus.

Authors:  K Itoh; S Y Sokol
Journal:  Genes Dev       Date:  1999-09-01       Impact factor: 11.361

2.  Stromelysin-1 (MMP-3) is a target and a regulator of Wnt1-induced epithelial-mesenchymal transition (EMT).

Authors:  Laurence Blavier; Alisa Lazaryev; Xiang-He Shi; Frederick J Dorey; Gregory M Shackleford; Yves A DeClerck
Journal:  Cancer Biol Ther       Date:  2010-07-29       Impact factor: 4.742

3.  Wnt11 signaling promotes proliferation, transformation, and migration of IEC6 intestinal epithelial cells.

Authors:  Lillian Ouko; Thomas R Ziegler; Li H Gu; Leonard M Eisenberg; Vincent W Yang
Journal:  J Biol Chem       Date:  2004-04-14       Impact factor: 5.157

4.  Rescue of a Wnt mutation by an activated form of LEF-1: regulation of maintenance but not initiation of Brachyury expression.

Authors:  J Galceran; S C Hsu; R Grosschedl
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-10       Impact factor: 11.205

5.  Regulation of breast cancer-induced bone lesions by β-catenin protein signaling.

Authors:  Yan Chen; Heidi Y Shi; Stuart R Stock; Paula H Stern; Ming Zhang
Journal:  J Biol Chem       Date:  2011-10-18       Impact factor: 5.157

6.  WNT10B functional dualism: beta-catenin/Tcf-dependent growth promotion or independent suppression with deregulated expression in cancer.

Authors:  Hirohide Yoshikawa; Kenichi Matsubara; Xiaoling Zhou; Shu Okamura; Takahiko Kubo; Yaeko Murase; Yuko Shikauchi; Manel Esteller; James G Herman; Xin Wei Wang; Curtis C Harris
Journal:  Mol Biol Cell       Date:  2007-08-29       Impact factor: 4.138

7.  Expression of Wnt, Frizzled, sFRP, and DKK genes in adult human pancreas.

Authors:  R Scott Heller; Tino Klein; Zhidong Ling; Harry Heimberg; Masaru Katoh; Ole D Madsen; Palle Serup
Journal:  Gene Expr       Date:  2003

8.  Differential recruitment of Dishevelled provides signaling specificity in the planar cell polarity and Wingless signaling pathways.

Authors:  J D Axelrod; J R Miller; J M Shulman; R T Moon; N Perrimon
Journal:  Genes Dev       Date:  1998-08-15       Impact factor: 11.361

9.  The N- or C-terminal domains of DSH-2 can activate the C. elegans Wnt/beta-catenin asymmetry pathway.

Authors:  Ryan S King; Stephanie L Maiden; Nancy C Hawkins; Ambrose R Kidd; Judith Kimble; Jeff Hardin; Timothy D Walston
Journal:  Dev Biol       Date:  2009-01-23       Impact factor: 3.582

10.  Gene expression analysis of macrophages that facilitate tumor invasion supports a role for Wnt-signaling in mediating their activity in primary mammary tumors.

Authors:  Laureen S Ojalvo; Charles A Whittaker; John S Condeelis; Jeffrey W Pollard
Journal:  J Immunol       Date:  2009-12-16       Impact factor: 5.422

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