| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2041589 | Cell Reports | 2014 | 14 Pages |
•We generated the first mice with reduced whole-body expression of Sox4•Sox4-deficient mice age prematurely and are cancer resistant•Sox4 deletion specifically in the skin leads to stem cell quiescence and more damage•Our expression analysis places Sox4 in the β-catenin/Wnt pathway of HFSC activation
SummarySox4 expression is restricted in mammals to embryonic structures and some adult tissues, such as lymphoid organs, pancreas, intestine, and skin. During embryogenesis, Sox4 regulates mesenchymal and neural progenitor survival, as well as lymphocyte and myeloid differentiation, and contributes to pancreas, bone, and heart development. Aberrant Sox4 expression is linked to malignant transformation and metastasis in several types of cancer. To understand the role of Sox4 in the adult organism, we first generated mice with reduced whole-body Sox4 expression. These mice display accelerated aging and reduced cancer incidence. To specifically address a role for Sox4 in adult stem cells, we conditionally deleted Sox4 (Sox4cKO) in stratified epithelia. Sox4cKO mice show increased skin stem cell quiescence and resistance to chemical carcinogenesis concomitantly with downregulation of cell cycle, DNA repair, and activated hair follicle stem cell pathways. Altogether, these findings highlight the importance of Sox4 in regulating adult tissue homeostasis and cancer.
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