| First Author | Viala S | Year | 2024 |
| Journal | Mol Biol Cell | Volume | 35 |
| Issue | 2 | Pages | br5 |
| PubMed ID | 37991903 | Mgi Jnum | J:346587 |
| Mgi Id | MGI:7618213 | Doi | 10.1091/mbc.E23-03-0111 |
| Citation | Viala S, et al. (2024) LGN loss randomizes spindle orientation and accelerates tumorigenesis in PTEN-deficient epidermis. Mol Biol Cell 35(2):br5 |
| abstractText | Loss of cell polarity and disruption of tissue organization are key features of tumorigenesis that are intrinsically linked to spindle orientation. Epithelial tumors are often characterized by spindle orientation defects, but how these defects impact tumor formation driven by common oncogenic mutations is not fully understood. Here, we examine the role of spindle orientation in adult epidermis by deleting a key spindle regulator, LGN, in normal tissue and in a PTEN-deficient mouse model. We report that LGN deficiency in PTEN mutant epidermis leads to a threefold increase in the likelihood of developing tumors on the snout, and an over 10-fold increase in tumor burden. In this tissue, loss of LGN alone increases perpendicular and oblique divisions of epidermal basal cells, at the expense of a planar orientation of division. PTEN loss alone does not significantly affect spindle orientation in these cells, but the combined loss of PTEN and LGN fully randomizes basal spindle orientation. A subset of LGN- and PTEN-deficient animals have increased amounts of proliferative spinous cells, which may be associated with tumorigenesis. These results indicate that loss of LGN impacts spindle orientation and accelerates epidermal tumorigenesis in a PTEN-deficient mouse model. |
