Chibby1 knockdown promotes mesenchymal-to-epithelial transition-like changes.

Cell cycle (Georgetown, Tex.)

PubMedID: 28107095

Fischer V, Wong M, Li FQ, Takemaru KI. Chibby1 knockdown promotes mesenchymal-to-epithelial transition-like changes. Cell Cycle. 2017;0.
Chibby1 (Cby1) was originally isolated as a binding partner for ß-catenin, a dual function protein in cell-cell adhesion and in canonical Wnt signaling. The canonical Wnt/ß-catenin pathway is dysregulated in various diseases including cancer, most notably of the gastrointestinal origin. To investigate the role of Cby1 in colorectal tumorigenesis, we generated stable Cby1-knockdown (KD) SW480 colon cancer cells. Unexpectedly, we found that Cby1 KD induces mesenchymal-to-epithelial transition (MET)-like changes in SW480 as well as in HEK293 cells. Cby1-KD cells displayed a cuboidal epithelial morphology with tight cell-cell contacts. In Cby1-KD cells, the plasma membrane localization of E-cadherin and ß-catenin was dramatically increased with formation of cortical actin rings, while the levels of the mesenchymal marker vimentin were decreased. Consistent with these changes, in wound healing assays, Cby1-KD cells exhibited epithelial cell-like properties as they migrated collectively as epithelial sheets. Furthermore, the anchorage-independent growth of Cby1-KD cells was reduced as determined by soft agar assays. These findings suggest that chronic Cby1 KD in colon cancer cells may counteract tumor progression by promoting the MET process.