| Literature DB >> 25908636 |
Christina Michailidi1, Stamatios Theocharis2, Gerasimos Tsourouflis3, Vasiliki Pletsa4, Gregorios Kouraklis3, Efstratios Patsouris2, Athanasios G Papavassiliou1, Constantinos Troungos5.
Abstract
Colorectal cancer (CRC) is the third most common cancer in men and the second in women worldwide. CRC development is the result of genetic and epigenetic alterations accumulation in the epithelial cells of colon mucosa. In the present study, DNA methylation, an epigenetic event, was evaluated in tumoral and matching normal epithelium in a cohort of 61 CRC patients. The results confirmed and expanded knowledge for the tumor suppressor genes hMLH1, MGMT, APC, and CDH1. Promoter methylation was observed for all the examined genes in different percentage. A total of 71% and 10% of the examined cases were found to be methylated in two or more and in all genes, respectively. mRNA and protein levels were also evaluated. Promoter methylation of hMLH1, MGMT, APC, and CDH1 genes was present at the early stages of tumor's formation and it could also be detected in the normal mucosa. Correlations of the methylated genes with patient's age and tumor's clinicopathological characteristics were also observed. Our findings suggest that DNA methylation is a useful marker for tumor progression monitoring and that promoter methylation in certain genes is associated with more advanced tumor stage, poor differentiation, and metastasis.Entities:
Keywords: Colon cancer; CpG islands; epigenetics; methylation; methylation-specific PCR
Mesh:
Substances:
Year: 2015 PMID: 25908636 PMCID: PMC4935349 DOI: 10.1177/1535370215583800
Source DB: PubMed Journal: Exp Biol Med (Maywood) ISSN: 1535-3699