TGF-beta induces formation of F-actin cores and matrix degradation in human breast cancer cells via distinct signaling pathways.

Abstract:

:Transforming growth factor beta regulates many biological processes including cell motility and invasion. Podosomes are specialized F-actin rich structures found in normal cells, such as osteoclasts and macrophages. Tumor cells often form related structures called invadopodia that are thought to promote invasion and metastasis. Here we show that human breast cancer cells organize F-actin rich structures in response to transforming growth factor beta that colocalize with areas of extracellular matrix degradation. We further show that organizing the complex of proteins needed to form these structures requires signaling through phosphatidylinositide 3-kinase and Src kinase, while activating the proteases involved in degradation of extracellular matrix requires extracellular signal-regulated kinase signaling, and that each of these pathways is activated by transforming growth factor beta in CA1D human breast cancer cells.

journal_name

Exp Cell Res

authors

Mandal S,Johnson KR,Wheelock MJ

doi

10.1016/j.yexcr.2008.09.013

subject

Has Abstract

pub_date

2008-11-15 00:00:00

pages

3478-93

issue

19

eissn

0014-4827

issn

1090-2422

pii

S0014-4827(08)00364-9

journal_volume

314

pub_type

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