The main cause of MSI was the genetic variation or epigenetic alteration of DNA mismatch repair (MMR); therefore, we analyzed the main members of the MMR system, MutL homolog 1 (MLH1), MutS protein homolog 2 (MSH2), MutS Homolog 6 (MSH6), and PMS1 homolog 2 (PMS2) and found that they were associated with FASN expression, and the results revealed that the FASN and MMR genes were significantly positively correlated with 29 cancers (Figure 5C). This evidence concerns the gene PMS2 and cancer.