“…DNMT1 is chiefly responsible for DNA methylation homeostasis, whereas two other methyl transferases; i.e., DNMT3a and DNMT3b, primarily catalyze de novo hypermethylation (18). All three enzymes, DNMT1, DNMT3a, and DMNT3b, have been shown to be overexpressed in several tumor types, including colorectal cancer (14,19). Interestingly, both sporadic and FAP-related colon adenocarcinomas have common, for example, p16 and MGMT, as well as different, for example, PAX3, tumor-suppressor genes that are methylated, and hypermethylation seems to be a general feature of both sporadic and FAP-related carcinomas (20,21).…”