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Activation of focal adhesion kinase through an interaction with β4 integrin contributes to tumorigenicity of colon cancer
Author(s) -
Tai YuLing,
Lai IRue,
Peng YuJu,
Ding ShihTorng,
Shen TangLong
Publication year - 2016
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1002/1873-3468.12215
Subject(s) - focal adhesion , integrin , colorectal cancer , cancer research , ptk2 , cancer , phosphorylation , adhesion , chemistry , microbiology and biotechnology , medicine , biology , cell , protein kinase a , biochemistry , mitogen activated protein kinase kinase , organic chemistry
High expression of either β4 integrin or focal adhesion kinase ( FAK ) has been reported in human colon cancer. However, it remains unclear how β4 integrin together with FAK contributes to the tumorigenicity of colon cancer. Here, we demonstrate that the co‐overexpression of β4 integrin and FAK positively correlates with advanced stages of human colon cancer. Activated β4 integrin interacts with FAK and subsequently induces FAK phosphorylation at Tyr397. Furthermore, ablation of the β4 integrin/ FAK complex and/or FAK activation impair colon cancer cell proliferation, anchorage‐independent growth, and tumorigenicity. Our data indicate that the β4 integrin/ FAK complex and subsequent FAK activation are essential regulators during the tumorigenicity of colon cancer, and we suggest an alternative strategy for colon cancer therapy.