Polymorphisms in methylenetetrahydrofolate reductase gene (MTHFR) and the age of onset of sporadic colorectal adenocarcinoma

• Published in: International journal of colorectal disease Vol. 22; no. 7; pp. 757 - 763
• Main Authors: LIMA, Carmen S. P, NASCIMENTO, Helvia, BONADIA, Luciana C, TEORI, Maria T, COY, Claudio S. R, GOES, Juvenal R. N, COSTA, Fernando F, BERTUZZO, Carmen S
• Format: Journal Article
• Language: English
• Published: Heidelberg Springer 01-07-2007; Berlin Springer Nature B.V
• Subjects: Adenocarcinoma; Adenocarcinoma - epidemiology; Adenocarcinoma - genetics; Adenocarcinoma - pathology; Age Factors; Age of Onset; Biological and medical sciences; Biomarkers, Tumor - genetics; Cancer; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - epidemiology; Colorectal Neoplasms - genetics; Colorectal Neoplasms - pathology; DNA, Neoplasm - genetics; Female; Folic acid; Gastroenterology. Liver. Pancreas. Abdomen; Genotype; Genotype & phenotype; Humans; Male; Medical sciences; Methylenetetrahydrofolate reductase; Methylenetetrahydrofolate Reductase (NADPH2) - genetics; Middle Aged; Neoplasm Staging; Polymerase Chain Reaction; Polymorphism, Genetic; Prognosis; Retrospective Studies; Risk Factors; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tumors; South America; Brazil; America; Rectal disease; Sporadic; Colorectal adenocarcinoma; MTHFR polymorphism; Colorectal cancer; Malignant tumor; Epidemiology; Colonic disease; Polymerase chain reaction; Age of onset; Digestive diseases; Intestinal disease; Molecular biology; Polymorphism
• ISSN: 0179-1958; 1432-1262
• DOI: 10.1007/s00384-006-0237-z

Evidence is accumulating for a role of folate in the aetiology of colorectal cancer (CRC). The methylenetetrahydrofolate reductase (MTHFR) gene, involved in folate metabolism, is polymorphic in humans. Since it is unknown whether the MTHFR C677T and A1298C polymorphisms alter the risk for CRC, this was the aim of our study.
Genomic DNA from 102 sporadic colorectal adenocarcinoma (SCA) patients and 300 controls was analyzed by polymerase chain reaction followed by restriction digestion for the polymorphisms analyses.
The frequencies of MTHFR C677T and A1298C genotypes were similar in patients and controls. Similar overall risks for disease were seen in individuals with the distinct MTHFR genotypes. However, an excess of the MTHFR 677TT and 677CT genotypes was seen in patients under 50 years, compared with patients at an older age (19.2 vs 13.1% and 61.6 vs 39.5%, respectively; P = 0.04). The differences were more prominent when the frequency of the 677TT plus 677CT genotype was seen in both group of patients (80.8 vs 52.6%, respectively; P = 0.01), and in younger patients compared to controls (80.8 vs 52.3%, P < 0.01). Individuals with the combined genotype had 3.82-fold (95% confidence interval, 1.41-10.42) increased risk of developing SCA under 50 years, compared with those harboring the wild-type genotype.
These results suggest a role for the MTHFR 677TT plus 677CT genotype in increasing SCA diagnosed at a low age in southeastern Brazil, but additional studies with larger sample sizes should be carried out to clarify this issue.