The results showed that immune response and inflammation-related biological functions associated with low-risk groups included “Inflammatory response,” “Cytokine receptor activity,” “Cytokine- cytokine receptor interaction,” “JAK-STAT pathway,” “Macrophage activation,” and “Cytokine receptor activity.” Tumor protective functions such as “DNA replication,” “MYC targets,” “Nucleotide excision repair,” “Cell cycle,” “Microtubule cytoskeleton organization involved mitosis,” and “Spliceosome” were activated in the high-risk group and predicted their poor prognosis. This evidence concerns the gene SOAT1 and neoplasm.