• Where do we go from here?
    • Understanding that:
      • There is considerable diversity in the expression dynamics of p53 target genes
      • This diversity is p53 dependent
      • Results are consistent with model prediction that mRNA decay rate determines gene expression dynamics

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        Current approaches for p53 targeting

    • What experiment could be performed to verify that p53 pulsing generate diversity in dynamics?
      • Next step in discovering how to arrest the cell cycle in cancer prevention methods
    • A better understanding of how signaling dynamics are regulated and how they affect cellular responses will provide new insights for manipulating them in a controlled way
    • In addition, targeted perturbation of protein dynamics, may enable new pharmacological strategies for altering cell fate in a range of diseases
    • Understanding the undercurrents of the cells and genes could also assist in best understanding how to prevent uncontrollable cell growth
Structure of Small-Molecule p53 Activators, Reactivators, and Inhibitors.

Structure of Small-Molecule p53 Activators, Reactivators, and Inhibitors.