It was clearly visualized that the risk genes PPARG and LHX1 were negatively correlated with anti-tumor effectors (e.g., CD8 T cells and activated memory CD4 T cells), positively correlated with primitive or resting immune cells (e.g., naive B cells, memory B cells, naive CD4 T cells, resting memory CD4 T cells and M0 macrophages), while the protective gene LCK was positively correlated with anti-tumor effectors (CD8 T cells, activated memory CD4 T cells, follicular helper T cells and M1 macrophages; Figures 8A–C). This evidence concerns the gene CD4 and neoplasm.