A p120 catenin isoform switch affects Rho activity, induces tumor cell invasion and predicts metastatic disease

Authors:
Yanagisawa M, Huveldt D, Kreinest P, Lohse CM, Cheville JC, Parker AS, Copland JA, Anastasiadis PZ
In:
Source: J Biol Chem
Publication Date: (2008)
Issue: 283(26): 18344-54
Research Area:
Cancer Research/Cell Biology
Cells used in publication:
MDA-MB-231
Species: human
Tissue Origin: breast
Platform:
Nucleofectorâ„¢ I/II/2b
Abstract
p120 catenin is a cadherin associated protein that regulates Rho GTPases and promotes the invasiveness of E-cadherin deficient cancer cells. Multiple p120 isoforms are expressed in cells via alternative splicing, and all of them are essential for HGF signaling to Rac1. However, only full-length p120 (isoform 1) promotes invasiveness. This selective ability of p120 isoform 1 is mediated by reduced RhoA activity, both under basal conditions and following HGF treatment. All p120 isoforms can bind RhoA in vitro, via a central RhoA binding site. However, only the co-operative binding of RhoA to the central p120 domain and to the alternatively spliced p120 N-terminus, stabilizes RhoA binding and inhibits RhoA activity. Consistent with this, increased expression of p120 isoform 1, when compared to other p120 isoforms, is predictive of renal tumor micrometastasis and systemic progression, following nephrectomy. Furthermore, ectopic expression of the RhoA-binding, N-terminal domain of p120 is sufficient to block the ability of p120 isoform 1 to inhibit RhoA, and to promote invasiveness. The data indicate that the increased expression of p120 isoform 1 during tumor progression contributes to the invasive phenotype of cadherin-deficient carcinomas, and that the N-terminal domain of p120 is a valid therapeutic target.