The Breakthrough Breast Cancer Research Centre, Division of Breast Cancer Research, Institute of Cancer Research, London, UK.
J Natl Cancer Inst. 2012 May 2;104(9):657-69. doi: 10.1093/jnci/djs156. Epub 2012 Apr 3.
Epidemiological studies have provided strong evidence for a role of endogenous sex steroids in the etiology of breast cancer. Our aim was to identify common variants in genes involved in sex steroid synthesis or metabolism that are associated with hormone levels and the risk of breast cancer in premenopausal women.
We measured urinary levels of estrone glucuronide (E1G) using a protocol specifically developed to account for cyclic variation in hormone levels during the menstrual cycle in 729 healthy premenopausal women. We genotyped 642 single-nucleotide polymorphisms (SNPs) in these women; a single SNP, rs10273424, was further tested for association with the risk of breast cancer using data from 10 551 breast cancer case patients and 17 535 control subjects. All statistical tests were two-sided.
rs10273424, which maps approximately 50 kb centromeric to the cytochrome P450 3A (CYP3A) gene cluster at chromosome 7q22.1, was associated with a 21.8% reduction in E1G levels (95% confidence interval [CI] = 27.8% to 15.3% reduction; P = 2.7 × 10(-9)) and a modest reduction in the risk of breast cancer in case patients who were diagnosed at or before age 50 years (odds ratio [OR] = 0.91, 95% CI = 0.83 to 0.99; P = .03) but not in those diagnosed after age 50 years (OR = 1.01, 95% CI = 0.93 to 1.10; P = .82).
Genetic variation in noncoding sequences flanking the CYP3A locus contributes to variance in premenopausal E1G levels and is associated with the risk of breast cancer in younger patients. This association may have wider implications given that the most predominantly expressed CYP3A gene, CYP3A4, is responsible for metabolism of endogenous and exogenous hormones and hormonal agents used in the treatment of breast cancer.
流行病学研究为内源性性激素在乳腺癌发病机制中的作用提供了有力证据。我们的目的是确定参与性激素合成或代谢的基因中的常见变体,这些变体与绝经前妇女的激素水平和乳腺癌风险相关。
我们使用专门制定的方案测量了 729 名健康绝经前女性月经周期中激素水平周期性变化的雌酮葡萄糖醛酸苷(E1G)水平。我们对这些女性进行了 642 个单核苷酸多态性(SNP)的基因分型;一个单核苷酸多态性 rs10273424 进一步使用来自 10551 例乳腺癌病例患者和 17535 例对照患者的数据进行了与乳腺癌风险的关联测试。所有统计检验均为双侧检验。
rs10273424 位于染色体 7q22.1 处细胞色素 P450 3A(CYP3A)基因簇约 50kb 着丝粒侧,与 E1G 水平降低 21.8%相关(95%置信区间 [CI] = 27.8%至 15.3%降低;P = 2.7×10(-9)),并且在 50 岁或之前被诊断为乳腺癌的病例患者中,乳腺癌风险适度降低(比值比 [OR] = 0.91,95%CI = 0.83 至 0.99;P = 0.03),但在 50 岁以后被诊断为乳腺癌的病例患者中,乳腺癌风险没有降低(OR = 1.01,95%CI = 0.93 至 1.10;P = 0.82)。
CYP3A 基因座侧翼非编码序列的遗传变异导致绝经前 E1G 水平的差异,并与年轻患者的乳腺癌风险相关。鉴于最主要表达的 CYP3A 基因 CYP3A4 负责内源性和外源性激素以及用于治疗乳腺癌的激素药物的代谢,这种关联可能具有更广泛的意义。