Open Access

ARTICLE

DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil

by ELEONIDAS MOURA LIMA, MARIANA FERREIRA LEAL, MARÍLIA DE ARRUDA CARDOSO SMITH, ROMMEL RODRÍGUEZ BURBANO, PAULO PIMENTEL DE ASSUMPÇÃO, MARIA JOSE BELLO, JUAN ANTONIO REY, FRANCINALDO FERREIRA DE LIMA, CACILDA CASARTELLI

1 Colegiado de Biomedicina, Universidade Federal do Piauí, Parnaíba, PI, Brasil;
2 Departamento de Genética, Faculdade de Medicina de Ribeirão Preto, Ribeirão Preto, Brasil.
3 Departamento de Morfologia, Escola Paulista de Medicina, São Paulo, Brasil;
4 Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, Brasil;
5 Serviço de Cirurgia, Hospital João de Barros Bar reto, Belém, Brasil;
6 Instituto de Investigaciones Biomedicas; Madri, Espanha;
7 Colegiado de Ciências Biológicas, Universidade Federal do Pará, Altamira, Brasil;
Address correspondence to: Mariana Ferreira Leal. Disciplina de Genética, Departamento de Morfologia e Genética. Universidade Federal de Sao Paulo. Rua Botucatu, 740. CEP 04023-900, Sao Paulo, BRASIL. Fax: (+55 11) 55764260. E-mail: mariana.morf@epm.br

BIOCELL 2008, 32(3), 237-243. https://doi.org/10.32604/biocell.2008.32.237

Abstract

Gastric cancer is one of the most common malignancies. DNA methylation is implicated in DNA mismatch repair genes deficiency. In the present study, we evaluated the methylation status of MLH1, MSH2, MSH6 and PMS2 in 20 diffuse- and 26 intestinal-type gastric cancer samples and 20 normal gastric mucosal of gastric cancer patients from Northern Brazil. We found that none of the nonneoplastic samples showed methylation of any gene promoter and 50% of gastric cancer samples showed at least one methylated gene promoter. Methylation frequencies of MLH1, MSH2, MSH6 and PMS2 promoter were 21.74%, 17.39%, 0% and 28.26% respectively in gastric cancer samples. MLH1 and PMS2 methylation were associated with neoplastic samples compared to nonneoplastic ones. PMS2 methylation was associated with diffuse- and intestinal-type cancer compared with normal controls. Intestinal-type cancer showed significant association with MLH1 methylation. Diffuse-type cancer was significantly associated with MSH2 methylation. Our findings show differential gene methylation in tumoral tissue, which allows us to conclude that methylation is associated with gastric carcinogenesis. Methylation of mismatch repair genes was associated with gastric carcinogenesis and may be a helpful tool for diagnosis, prognosis and therapies. However, MSH6 does not seem to be regulated by methylation in our samples.

---

Keywords

---

Citations