Polymorphism of cytosolic serine hydroxymethyltransferase, estrogen and breast cancer risk among Chinese women in Taiwan
Journal
Breast Cancer Research and Treatment
Journal Volume
111
Journal Issue
1
Pages
145-155
Date Issued
2008
Author(s)
Abstract
Cytosolic serine hydroxymethyltransferase (cSHMT) is key to intersection of folate-metabolic pathway, participating in the pyrimidine synthesis for DNA repair. Based on the hypothesis that variants of the cSHMT C1420T together with methionine synthase (MS A2756G) and 5,10-methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) are associated with breast cancer, we performed a multigenic case-control study of the effects to breast cancer risk of four polymorphisms of folate-metabloizing genes against duration of estrogen exposure. Support of our hypothesis came from the following observations: (i) Allelic frequency of cSHMT C1420T was higher in the controls than in the cases, manifesting a 0.56-fold risk reduction in breast cancer (95%CI = 0.39-0.80); and this association was more significant in those women are susceptible to time of estrogen exposure. (ii) A joint effect of the cSHMT and MS polymorphisms significantly reduced susceptibility to breast cancer (aOR = 0.55; 95%CI = 0.34-0.88). (iii) There was a trend toward a reduced risk of breast cancer in women carrying a greater number of putative low-risk genotypes (P trend = 0.048). (iv) This synergistic effects on risk reduction was significantly interacted with length of estrogen exposure, exhibiting a longer time of estrogen exposure (?30 years), menarche-to-FFTP interval (>11 years), age at the first full-term pregnancy (?25 years), and body mass index (?24). In conclusion, our study provides support to account for the preferential role of cSHMT polymorphism to lower risk of female breast cancer, and such reduced risk would be more significant in carriers with the polymorphisms of MS and MTHFR genes. ? 2007 Springer Science+Business Media, LLC.
SDGs
Other Subjects
5,10 methylenetetrahydrofolate reductase (FADH2); estrogen; folic acid; glycine hydroxymethyltransferase; methionine synthase; adult; aged; article; body mass; breast cancer; cancer risk; cancer susceptibility; case control study; Chinese; controlled study; DNA repair; female; gene frequency; gene interaction; genetic polymorphism; genotype; human; major clinical study; menarche; pregnancy; priority journal; pyrimidine synthesis; Taiwan; 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Asian Continental Ancestry Group; Breast Neoplasms; Case-Control Studies; Estrogens; Female; Genetic Predisposition to Disease; Genotype; Glycine Hydroxymethyltransferase; Humans; Maternal Age; Menarche; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Pregnancy; Risk Factors; Taiwan
Type
journal article