What it is
Although tumor protein p53 (TP53) mutations are among the most common lesions in epithelial cancers, how p53 loss drives unrestrained clonal expansion remains unclear. Working with mouse epidermis, we found that p53 suppresses clonal expansion by limiting progenitor self-renewal.
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Filed underCancer-related Molecular Pathways, Wnt/β-catenin signaling in development and cancer, Developmental Biology and Gene Regulation