In contrary we found upregulated (EOMES, TNFSFR9, TIGIT, KLRD1) and downregulated genes (PAG1, GNLY, ANXA1, FGFBP2) that are involved in tumor escape from immune surveillance by suppressing T-cells or by reprogramming T-cells toward T-cell exhaustion. This evidence concerns the gene EOMES and neoplasm.