p140Cap protein suppresses tumour cell properties, regulating Csk and Src kinase activity

被引:68
作者
Di Stefano, Paola
Damiano, Laura
Cabodi, Sara
Aramu, Simona
Tordella, Luca
Praduroux, Alice
Piva, Roberto
Cavallo, Federica
Forni, Guido
Silengo, Lorenzo
Tarone, Guido
Turco, Emilia
Defilippi, Paola
机构
[1] Univ Turin, Ctr Mol Biotechnol, I-10126 Turin, Italy
[2] Univ Turin, Ctr Expt Res & Med Studies, I-10126 Turin, Italy
关键词
cell signalling; invasion; motility; p140Cap; tumour growth;
D O I
10.1038/sj.emboj.7601724
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We recently identified p140Cap as a novel adaptor protein, expressed in epithelial-rich tissues and phosphorylated upon cell matrix adhesion and growth factor treatment. Here, we characterise p140Cap as a novel Src-binding protein, which regulates Src activation via C-terminal Src kinase (Csk). p140Cap silencing increases cell spreading, migration rate and Src kinase activity. Accordingly, increased expression of p140Cap activates Csk, leading to inhibition of Src and downstream signalling as well as of cell motility and invasion. Moreover, cell proliferation and 'in vivo' breast cancer cell growth are strongly impaired by high levels of p140Cap, providing the first evidence that p140Cap is a novel negative regulator of tumour growth.
引用
收藏
页码:2843 / 2855
页数:13
相关论文
共 42 条
[1]   Src-induced de-regulation of E-cadherin in colon cancer cells requires integrin signalling [J].
Avizienyte, E ;
Wyke, AW ;
Jones, RJ ;
McLean, GW ;
Westhoff, MA ;
Brunton, VG ;
Frame, MC .
NATURE CELL BIOLOGY, 2002, 4 (08) :632-638
[2]   Loss of β4 integrin subunit reduces the tumorigenicity of MCF7 mammary cells and causes apoptosis upon hormone deprivation [J].
Bon, Giulia ;
Folgiero, Valentina ;
Bossi, Gianluca ;
Felicioni, Laura ;
Marchetti, Antonio ;
Sacchi, Ada ;
Falcioni, Rita .
CLINICAL CANCER RESEARCH, 2006, 12 (11) :3280-3287
[3]   Functions of the adapter protein Cas: signal convergence and the determination of cellular responses [J].
Bouton, AH ;
Riggins, RB ;
Bruce-Staskal, PJ .
ONCOGENE, 2001, 20 (44) :6448-6458
[4]   Src and Ras are involved in separate pathways in epithelial cell scattering [J].
Boyer, B ;
Roche, S ;
Denoyelle, M ;
Thiery, JP .
EMBO JOURNAL, 1997, 16 (19) :5904-5913
[5]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[6]   Identification of Src-specific phosphorylation site on focal adhesion kinase: Dissection of the role of Src SH2 and catalytic functions and their consequences for tumor cell behavior [J].
Brunton, VG ;
Avizienyte, E ;
Fincham, VJ ;
Serrels, B ;
Metcalf, CA ;
Sawyer, TK ;
Frame, MC .
CANCER RESEARCH, 2005, 65 (04) :1335-1342
[7]   Rho and Rac take center stage [J].
Burridge, K ;
Wennerberg, K .
CELL, 2004, 116 (02) :167-179
[8]   A PKC-η/Fyn-Dependent pathway leading to keratinocyte growth arrest and differentiation [J].
Cabodi, S ;
Calautti, E ;
Talora, C ;
Kuroki, T ;
Stein, PL ;
Dotto, GP .
MOLECULAR CELL, 2000, 6 (05) :1121-1129
[9]   p130Cas interacts with estrogen receptor α and modulates non-genomic estrogen signaling in breast cancer cells [J].
Cabodi, S ;
Moro, L ;
Baj, G ;
Smeriglio, M ;
Di Stefano, P ;
Gippone, S ;
Surico, N ;
Silengo, L ;
Turco, E ;
Tarone, G ;
Defilippi, P .
JOURNAL OF CELL SCIENCE, 2004, 117 (08) :1603-1611
[10]  
CABODI S, 2006, INTEGRINS DEV, P49