CD4 and neoplasm: Correlation analyses of the glycogene-related signatures with immunocyte infiltration were conducted to explore the impact of our model on the tumour microenvironment of patients with KIRC (Figure 9(A)), indicating that this signature positively correlated with the infiltration levels of resting dendritic cells, macrophages M1, macrophages M2, monocytes, resting NK cells, and resting CD4 memory T cells.