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Turnover of Focal Adhesions and Cancer Cell Migration
Author(s) -
Makoto Nagano,
Daisuke Hoshino,
Naohiko Koshikawa,
Toshifumi Akizawa,
Motoharu Seiki
Publication year - 2012
Publication title -
international journal of cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 53
eISSN - 1687-8884
pISSN - 1687-8876
DOI - 10.1155/2012/310616
Subject(s) - focal adhesion , extracellular matrix , integrin , microbiology and biotechnology , cell migration , cell adhesion , adhesion , regulator , cell , biology , chemistry , signal transduction , biochemistry , gene , organic chemistry
Cells are usually surrounded by the extracellular matrix (ECM), and adhesion of the cells to the ECM is a key step in their migration through tissues. Integrins are important receptors for the ECM and form structures called focal adhesions (FAs). Formation and disassembly of FAs are regulated dynamically during cell migration. Adhesion to the ECM has been studied mainly using cells cultured on an ECM-coated substratum, where the rate of cell migration is determined by the turnover of FAs. However, the molecular events underlying the disassembly of FAs are less well understood. We have recently identified both a new regulator of this disassembly process and its interaction partners. Here, we summarize our understanding of FA disassembly by focusing on the proteins implicated in this process.

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