Mathematical analysis of a SIPC age-structured model of cervical cancer.

Human Papillomavirus (HPV), which is the main causal factor of cervical cancer, infects normal cervical cells on the specific cell's age interval, i.e., between the G1 to S phase of cell cycle. Hence, the spread of the viruses in cervical tissue not only depends on the time, but also the cell age. By this fact, we introduce a new model that shows the spread of HPV infections on the cervical tissue by considering the age of cells and the time. The model is a four dimensional system of the first order partial differential equations with time and age independent variables, where the cells population is divided into four sub-populations, i.e., susceptible cells, infected cells by HPV, precancerous cells, and cancer cells. There are two types of the steady state solution of the system, i.e., disease-free and cancerous steady state solutions, where the stability is determined by using Fatou's lemma and solving some integral equations. In this case, we use a non-standard method to calculate the basic reproduction number of the system. Lastly, we use numerical simulations to show the dynamics of the age-structured system.

The Dynamics of HPV Infection and Cervical Cancer Cells.

The development of cervical cells from normal cells infected by human papillomavirus into invasive cancer cells can be modeled using population dynamics of the cells and free virus. The cell populations are separated into four compartments: susceptible cells, infected cells, precancerous cells and cancer cells. The model system of differential equations also has a free virus compartment in the system, which infect normal cells. We analyze the local stability of the equilibrium points of the model and investigate the parameters, which play an important role in the progression toward invasive cancer. By simulation, we investigate the boundary between initial conditions of solutions, which tend to stable equilibrium point, representing controlled infection, and those which tend to unbounded growth of the cancer cell population. Parameters affected by drug treatment are varied, and their effect on the risk of cancer progression is explored.