Dynamic behavior of the p53-Mdm2 core module under the action of drug Nutlin and dual delays.

Abstract

Nutlin is a family of p53-targeting drugs. It is able to bind to Mdm2, thereby accelerate the accumulation of p53 that is a prominent tumor suppressor. An integrated module of the Nutlin PBK and p53 pathway is composed of positive feedback mediated by Mdm2 mRNA as well as the drug Nutlin and negative feedback mediated by Mdm2 protein. The main research content of our paper is how the time delay of protein synthesis, response time delay of Nutlin drug, the degradation rate of Mdm2, the degradation rate of p53 depended on Mdm2 and the actual dose of Nutlin in the cell affect the oscillatory behavior caused by Hopf bifurcation in the integrated network system of Nutlin PBK and p53 pathways. The stability of the unique positive equilibrium point and the existence of Hopf bifurcation are studied by taking the time delays as the bifurcation parameters and applying bifurcation theory. Based on the normal form theory and central manifold theorem, explicit criteria to determine the Hopf bifurcation direction and stability of the bifurcated periodic solution are established. It is found that the time delays and key parameters in the integrated network system of Nutlin PBK and p53 pathways play an important role in the amplitude and period of p53 oscillation according to the results from the numerical simulation and theoretical calculation. These results may provide us with a better understanding of the biological functions of the p53 pathway and some clues for cancer treatment.