| Literature DB >> 34209614 |
Adélaïde Doray1, Roxane Lemoine1, Marc Severin2, Stéphanie Chadet1, Osbaldo Lopez-Charcas1, Audrey Héraud1, Christophe Baron1, Pierre Besson1, Arnaud Monteil3, Stine Falsig Pedersen2, Sébastien Roger1,4.
Abstract
The SCN4B gene, coding for the NaVβ4 subunit of voltage-gated sodium channels, was recently found to be expressed in normal epithelial cells and down-regulated in several cancers. However, its function in normal epithelial cells has not been characterized. In this study, we demonstrated that reducing NaVβ4 expression in MCF10A non-cancer mammary epithelial cells generated important morphological changes observed both in two-dimensional cultures and in three-dimensional cysts. Most notably, the loss of NaVβ4 induced a complete loss of epithelial organisation in cysts and increased proteolytic activity towards the extracellular matrix. Loss of epithelial morphology was associated with an increased degradation of β-catenin, reduced E-cadherin expression and induction of mesenchymal markers N-cadherin, vimentin, and α-SMA expression. Overall, our results suggest that Navβ4 may participate in the maintenance of the epithelial phenotype in mammary cells and that its downregulation might be a determining step in early carcinogenesis.Entities:
Keywords: NaVβ4; epithelial phenotype; epithelial-to-mesenchymal transition; mammary cells; β-catenin
Year: 2021 PMID: 34209614 DOI: 10.3390/cells10071624
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600