| Literature DB >> 33393839 |
Sarah Alsharif1, Pooja Sharma1, Karina Bursch1, Rachel Milliken1, Van Lam2, Arwa Fallatah1, Thuc Phan3, Meagan Collins1, Priya Dohlman1, Sarah Tiufekchiev1, Georges Nehmetallah3, Christopher B Raub2, Byung Min Chung1.
Abstract
A cytoskeletal protein keratin 19 (K19) is highly expressed in breast cancer but its effects on breast cancer cell mechanics are unclear. In MCF7 cells where K19 expression is ablated,we found that K19 is required to maintain rounded epithelial-like shape and tight cell-cell adhesion. A loss of K19 also lowered cell surface E-cadherin levels. Inhibiting internalization restored cell-cell adhesion of KRT19 knockout cells, suggesting that E-cadherin internalization contributed to defective adhesion. Ultimately, while K19 inhibited cell migration and invasion, it was required for cells to form colonies in suspension. Our results suggest that K19 stabilizes E-cadherin complexes at the cell membrane to maintain cell-cell adhesion which inhibits cell invasiveness but provides growth and survival advantages for circulating tumor cells.Entities:
Keywords: Intermediate filaments; adherens junction; breast cancer; cell migration; cell morphology; cell-cell adhesion; keratin; keratin 19; metastasis
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Year: 2021 PMID: 33393839 PMCID: PMC7801129 DOI: 10.1080/19336918.2020.1868694
Source DB: PubMed Journal: Cell Adh Migr ISSN: 1933-6918 Impact factor: 3.405