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
Molecular Biotechnology Center, University of Torino, Via Nizza 52, Turin 10126, Italy.
EMBO J. 2007 Jun 20;26(12):2843-55. doi: 10.1038/sj.emboj.7601724. Epub 2007 May 24.
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.
我们最近鉴定出p140Cap是一种新型衔接蛋白,在富含上皮细胞的组织中表达,并在细胞与基质黏附及生长因子处理后发生磷酸化。在此,我们将p140Cap表征为一种新型Src结合蛋白,它通过C末端Src激酶(Csk)调节Src激活。p140Cap沉默会增加细胞铺展、迁移速率和Src激酶活性。相应地,p140Cap表达增加会激活Csk,导致Src及下游信号传导以及细胞运动性和侵袭受到抑制。此外,高水平的p140Cap会严重损害细胞增殖和“体内”乳腺癌细胞生长,这首次证明p140Cap是肿瘤生长的新型负调节因子。