A RhoG-mediated signaling pathway that modulates invadopodia dynamics in breast cancer cells.

Abstract:

:One of the hallmarks of cancer is the ability of tumor cells to invade surrounding tissues and metastasize. During metastasis, cancer cells degrade the extracellular matrix, which acts as a physical barrier, by developing specialized actin-rich membrane protrusion structures called invadopodia. The formation of invadopodia is regulated by Rho GTPases, a family of proteins that regulates the actin cytoskeleton. Here, we describe a novel role for RhoG in the regulation of invadopodia disassembly in human breast cancer cells. Our results show that RhoG and Rac1 have independent and opposite roles in the regulation of invadopodia dynamics. We also show that SGEF (also known as ARHGEF26) is the exchange factor responsible for the activation of RhoG during invadopodia disassembly. When the expression of either RhoG or SGEF is silenced, invadopodia are more stable and have a longer lifetime than in control cells. Our findings also demonstrate that RhoG and SGEF modulate the phosphorylation of paxillin, which plays a key role during invadopodia disassembly. In summary, we have identified a novel signaling pathway involving SGEF, RhoG and paxillin phosphorylation, which functions in the regulation of invadopodia disassembly in breast cancer cells.

journal_name

J Cell Sci

journal_title

Journal of cell science

authors

Goicoechea SM,Zinn A,Awadia SS,Snyder K,Garcia-Mata R

doi

10.1242/jcs.195552

subject

Has Abstract

pub_date

2017-03-15 00:00:00

pages

1064-1077

issue

6

eissn

0021-9533

issn

1477-9137

pii

jcs.195552

journal_volume

130

pub_type

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