Foxl1 is a mesenchymal Modifier of Min in carcinogenesis of stomach and colon.

Abstract:

:Constitutive activation of the Wnt/APC/beta-catenin pathway is a frequent initiating event in gastrointestinal carcinogenesis. Mutations in the Adenomatous Polyposis Coli (APC) gene up-regulate Wnt signaling by stabilizing beta-catenin and causing activation of targets important in proliferation control. Here we show that loss of the mesenchymal transcription factor Foxl1 leads to a marked increase in tumor multiplicity in the colon of Apc(Min) mice. Apc(Min/+);Foxl1-/- mice also develop gastric tumors not observed in Apc(Min) mice. These effects are caused by earlier tumor initiation due to accelerated loss of heterozygosity (LOH) at the Apc locus. Foxl1 is the first mesenchymal Modifier of Min and plays a key role in gastrointestinal tumorigenesis.

journal_name

Genes Dev

journal_title

Genes & development

authors

Perreault N,Sackett SD,Katz JP,Furth EE,Kaestner KH

doi

10.1101/gad.1260605

subject

Has Abstract

pub_date

2005-02-01 00:00:00

pages

311-5

issue

3

eissn

0890-9369

issn

1549-5477

pii

gad.1260605

journal_volume

19

pub_type

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