Active Src elevates the expression of beta-catenin by enhancement of cap-dependent translation.

Abstract:

:The proto-oncogene pp60(c-Src) (c-Src) is activated in many types of cancer and contributes to the transformed phenotype of the tumor, although its role is not yet fully understood. Here we report that active Src elevates the levels of beta-catenin by enhancing cap-dependent translation. Src induces phosphorylation of the eukaryotic initiation factor 4E via the Ras/Raf/ERK pathway and the phosphorylation of its inhibitor 4E-BP1 via the PI3K/mTOR pathway. Activated Src enhances the accumulation of nuclear beta-catenin and enhances its transcriptional activity, elevating target genes such as cyclin D1. This novel activation of the Wnt pathway by Src most probably contributes to the oncogenic phenotype of cancer cells.

journal_name

Mol Cell Biol

authors

Karni R,Gus Y,Dor Y,Meyuhas O,Levitzki A

doi

10.1128/MCB.25.12.5031-5039.2005

subject

Has Abstract

pub_date

2005-06-01 00:00:00

pages

5031-9

issue

12

eissn

0270-7306

issn

1098-5549

pii

25/12/5031

journal_volume

25

pub_type

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