TP53 is the most frequently mutated gene in human
cancer. Functionally, p53 is activated by a host of stress stimuli and, in turn,
governs an exquisitely complex anti-proliferative transcriptional program that
touches upon a bewildering array of biological responses. Despite the many
unveiled facets of the p53 network, a clear appreciation of how and in what
contexts p53 exerts its diverse effects remains unclear. How can we interpret
p53’s disparate activities and the consequences of its dysfunction to
understand how cell type, mutation profile, and epigenetic cell state dictate
outcomes, and how might we restore its tumor suppressive activities in
cancer?