This, coupled with increased PD-L1 on tumor cells (60), could lead to an enhanced PD-1/PD-L1 signaling (61), in which the interaction between PD-1/PD-L1 provides a possibility for the anergy, exhaustion, and apoptosis of tumor-reactive T cells (62), thereby, reducing cancer immune surveillance associated with senescent T cells (63). This evidence concerns the gene CD274 and cancer.