Sox4 Links Tumor Suppression to Accelerated Aging in Mice by Modulating Stem Cell Activation

Miguel Foronda; Paula Martínez; Stefan Schoeftner; Gonzalo Gómez-López; Ralph Schneider; Juana M. Flores; David G. Pisano; Maria A. Blasco

Sox4 Links Tumor Suppression to Accelerated Aging in Mice by Modulating Stem Cell Activation

2014

Sox4 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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