Mathematical investigation into the role of macrophage heterogeneity on the temporal and spatio-temporal dynamics of non-small cell lung cancers.

Non Small Cell Lung Cancer (NSCLC) is the most common type of lung cancer, and represents the leading cause of cancer-related deaths worldwide. Experimental studies have shown that these solid cancers are heavily infiltrated with macrophages: anti-tumour M1 macrophages, pro-tumour M2 macrophages, and macrophage subtypes sharing both M1 and M2 properties. In this study we aim to investigate qualitatively the role of macrophages with different functional phenotypes (especially those with mixed phenotypes) on cancer dynamics and the success of different immunotherapies for cancer. To this end, we start with two time-evolving mathematical models for cancer-immune interactions that consider: (i) the effect of the two extreme phenotypes, M1 and M2 cells; (ii) the effect of M1 and M2 cells, as well as a macrophage sub-population with a mixed phenotype (throughout this theoretical study we call these cells "M12 cells"). We compare the dynamics of the two models using computational approaches, paying particular attention to the effect of different anti-cancer immunotherapies that focus on macrophages. Since data available for NSCLC and macrophage interactions are incomplete, we perform a global sensitivity analysis to see the influence of input parameters on model outcomes. Finally, we consider extensions of the previous two models to include also the spatial movement of cells, and investigate the role of macrophages with extreme phenotypes and with mixed phenotypes, on the invasion of cancer cells into the surrounding extracellular matrix (ECM). We use numerical simulations to investigate the macrophages phenotypes at the tumour center versus the invasive margin. Again, we examine the impact of immunotherapies for cancer on the spatial dynamics of cancers and immune cells, and observe a shift in the phenotype of macrophages distributed at the tumour center and invasive margin.