Lixiang Sun, Xiaohui Xu, Yongjun Chen, Yuxia Zhou, Ran Tan, Hantian Qiu, Liting Jin, Wenyi Zhang, Rong Fan, Wanjin Hong, Tuanlao Wang
Oncogene 2018 JulThe small GTPase Rab34 regulates spatial distribution of the lysosomes, secretion, and macropinocytosis. In this study, we found that Rab34 is over-expressed in aggressive breast cancer cells, implying a potential role of Rab34 in breast cancer. Silencing Rab34 by shRNA inhibits cell migration, invasion, and adhesion of breast cancer cells. Rab34 specifically binds to the cytoplasmic tail of integrin β3, and depletion of Rab34 promotes the degradation of integrin β3. Interestingly, EGF induces the translocation of Rab34 to the membrane ruffle, which is greatly enhanced by the expression of Src kinase. Accordingly, Rab34 is tyrosine phosphorylated by Src at Y247 residue. A mutant mimicking phosphorylated form of Rab34 (Rab34Y247D) promotes cell migration and invasion. Importantly, the tyrosine phosphorylation of Rab34 is inhibited in cells in suspension, and increased with the cells re-adhesion. In addition, Rab34Y247D promotes cell adhesion, and enhances integrin β3 endocytosis and recycling. The results uncover a role of Rab34 in migration and invasion of breast cancer cells and its involvement in cancer metastasis, and provide a novel mechanism of tyrosine phosphorylation of Rab34 in regulating cell migration, invasion, and adhesion through modulating the endocytosis, stability, and recycling of integrin β3.
Lixiang Sun, Xiaohui Xu, Yongjun Chen, Yuxia Zhou, Ran Tan, Hantian Qiu, Liting Jin, Wenyi Zhang, Rong Fan, Wanjin Hong, Tuanlao Wang. Rab34 regulates adhesion, migration, and invasion of breast cancer cells. Oncogene. 2018 Jul;37(27):3698-3714
PMID: 29622794
View Full Text