Lifeng Feng, Jin-Tao Wang, Hongchuan Jin, Kaixian Qian, Jian-Guo Geng
Cell biochemistry and function 2011 OctThe binding of Cbl-interacting protein of 85 kDa (CIN85) to c-Cbl is important to endocytosis and degradation of epidermal growth factor receptor (EGFR). The proline-arginine motif PXXXPR in c-Cbl and SH3 domains of CIN85 are essential to this interaction. Here, we demonstrated that SH3KBP1-binding protein 1 (SHKBP1), which also contains two PXXXPR motifs, constitutively bound to SH3 domains of CIN85. Importantly, the binding of SHKBP1 prevented the interaction of CIN85 with c-Cbl and inhibited the translocation of CIN85 to EGFR-containing vesicles, thus reducing EGFR degradation and enhancing EGF-induced serum response element transcription activity. Therefore, our results indicated that SHKBP1 could promote EGFR signaling pathway by interrupting c-Cbl-CIN85 complex and inhibiting EGFR degradation. Copyright © 2011 John Wiley & Sons, Ltd.
Lifeng Feng, Jin-Tao Wang, Hongchuan Jin, Kaixian Qian, Jian-Guo Geng. SH3KBP1-binding protein 1 prevents epidermal growth factor receptor degradation by the interruption of c-Cbl-CIN85 complex. Cell biochemistry and function. 2011 Oct;29(7):589-96
PMID: 21830225
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