Song Ailing, Zhao Lei, Li Yumin, Wu Li, Li Yu, Liu Xiaokang, Lan Shen
Key Laboratory of Digestive System Tumors of Gansu Province, Gansu, People's Republic of China.
Depertment of Surgery, The Second Hospital of Lanzhou University, Lanzhou, Gansu, People's Republic of China.
IUBMB Life. 2016 Jul;68(7):526-34. doi: 10.1002/iub.1509. Epub 2016 May 30.
Elevated homocysteine levels are a risk factor for breast cancer, although the mechanism underlying this effect is unknown. Genome-wide association studies were used to systematically identify genetic variants which were significantly associated with the circulating homocysteine concentration. To examine the role of homocysteine-related variants in the occurrence of breast cancer, we investigated the association between these variants and breast cancer in a Han Chinese population. Five variants of genome-wide significant homocysteine-related genes were selected for the analysis in a case-control study, with a total of 487 patients with breast cancer and 605 controls. We found that none of the studied polymorphisms were related to the altered breast cancer risk. In the haplotypic analysis, the 5,10-methylenetetrahydrofolate reductase (MTHFR) haplotypes rs12085006A/rs1999594G/rs1801133C (OR = 3.44, 95% CI = 1.58-7.50, P = 0.0019) and rs12085006A/rs1999594G/rs1801133T (OR = 16.21, 95% CI = 2.19- 120.32, P = 0.0065) were significantly associated with an increased breast cancer risk when compared with the wild-type haplotype. Both of the risky MTHFR haplotypes were correlated with decreased MTHFR gene expression and elevated homocysteine concentrations, indicating a genetic component for hyperhomocysteinemia. The MTHFR haplotypes reconstructed with homocysteine-related variants were associated with the occurrence of breast cancer. This finding further emphasizes the importance of homocysteine metabolism genes in breast carcinogenesis and highlights the interplay of diet, genetics, and human cancers. © 2016 IUBMB Life, 68(7):526-534, 2016.
同型半胱氨酸水平升高是乳腺癌的一个风险因素,尽管这种效应背后的机制尚不清楚。全基因组关联研究被用于系统地识别与循环同型半胱氨酸浓度显著相关的基因变异。为了研究同型半胱氨酸相关变异在乳腺癌发生中的作用,我们在汉族人群中调查了这些变异与乳腺癌之间的关联。在一项病例对照研究中,选择了五个全基因组显著的同型半胱氨酸相关基因的变异进行分析,共有487例乳腺癌患者和605例对照。我们发现,所研究的多态性均与乳腺癌风险改变无关。在单倍型分析中,与野生型单倍型相比,5,10-亚甲基四氢叶酸还原酶(MTHFR)单倍型rs12085006A/rs1999594G/rs1801133C(OR = 3.44,95% CI = 1.58 - 7.50,P = 0.0019)和rs12085006A/rs1999594G/rs1801133T(OR = 16.21,95% CI = 2.19 - 120.32,P = 0.0065)与乳腺癌风险增加显著相关。两种有风险的MTHFR单倍型均与MTHFR基因表达降低和同型半胱氨酸浓度升高相关,表明高同型半胱氨酸血症存在遗传因素。用同型半胱氨酸相关变异重建的MTHFR单倍型与乳腺癌的发生有关。这一发现进一步强调了同型半胱氨酸代谢基因在乳腺癌发生中的重要性,并突出了饮食、遗传学和人类癌症之间的相互作用。© 2016国际生物化学与分子生物学联盟生命科学,68(7):526 - 534,2016。