Catechol-O-Methyltransferase (COMT) gene polymorphism and breast cancer risk in young women.
Catechol-O-Methyltransferase (COMT) gene polymorphism and breast cancer risk in young women.
复制标题
儿茶酚-O-甲基转移酶(COMT)基因多态性和年轻女性乳腺癌风险。
DOI:
10.1054/bjoc.2001.2009
复制
发表时间:
2001-09-14
影响因子:
8.8
通讯作者:
Wingren, S
中科院分区:
文献类型:
--
作者:
Bergman-Jungestrom, M;Wingren, S
Oestrogen exposure has long been considered to be a main risk factor of breast cancer. More recently, interest has also focused on the possible carcinogenic influence from oestrogen metabolites, such as catechol oestrogens. O-methylation, catalysed by Catechol-O-Methyltransferase (COMT), is one pathway by which the potentially carcinogenic catechol oestrogens can be inactivated. The gene coding for COMT protein contains a single-nucleotide polymorphism (SNP), resulting in an amino acid shift Val→Met, which has been shown to determine high- and low-activity configuration of the enzyme. We hypothesized that the low-activity allele, COMTMet, may be implicated in early onset breast cancer. In the present case–control study, including 126 young breast cancer patients (≤ 36 years) and 117 healthy female blood donors, we analysed the association between COMTMet genotype and risk of breast cancer. No significant difference in the frequency of low-/high-activity alleles was found between cases and controls, indicating that the polymorphism, as a single factor, may not contribute to breast carcinogenesis in young women. © 2001 Cancer Research Campaignhttp://www.bjcancer.com