Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, EPS-MSC 7234, 6120 Executive Boulevard, Bethesda, MD 20892-7234, USA.
Carcinogenesis. 2010 May;31(5):842-6. doi: 10.1093/carcin/bgq038. Epub 2010 Feb 19.
Biliary tract cancer encompasses tumors of the gallbladder, bile duct and ampulla of Vater. Gallbladder cancer is more common in women, whereas bile duct cancer is more common in men, suggesting that sex hormones may play a role in the etiology of these cancers. The intracellular action of estrogens is regulated by the estrogen receptor (ESR); thus, we examined the role of common genetic variants in ESR genes on the risk of biliary tract cancers and stones in a population-based case-control study in Shanghai, China (411 cancer cases, 895 stone cases and 786 controls). We genotyped six single-nucleotide polymorphisms (SNPs), four in ESR1 (rs2234693, rs3841686, rs2228480 and rs1801132) and two in ESR2 (rs1256049 and rs4986938). In all participants, the ESR1 rs1801132 (P325P) G allele was associated with excess risks of bile duct [odds ratio (OR) = 1.7, 95% confidence interval (CI) 1.1-2.8] and ampulla of Vater cancers (OR = 2.1, 95% CI 0.9-4.9) compared with the CC genotype. The association with bile duct cancer was apparent among men (OR = 2.8, 95% CI 1.4-5.7) but not among women (P-heterogeneity = 0.01). Also, the ESR2 rs4986938 (38 bp 3' of STP) GG genotype was associated with a higher risk of bile duct cancer (OR = 3.3, 95% CI 1.3-8.7) compared with the AA genotype, although this estimate was based on a small number of subjects. None of the other SNPs examined was associated with biliary tract cancers or stones. False discovery rate-adjusted P-values were not significant (P > 0.1). No association was found for ESR1 haplotype based on four SNPs. These preliminary results suggest that variants in ESR genes could play a role in the etiology of biliary tract cancers, especially bile duct cancer in men.
胆道癌包括胆囊、胆管和 Vater 壶腹的肿瘤。胆囊癌在女性中更为常见,而胆管癌在男性中更为常见,这表明性激素可能在这些癌症的病因学中发挥作用。雌激素的细胞内作用受雌激素受体(ESR)调节;因此,我们在中国上海进行了一项基于人群的病例对照研究,检查了 ESR 基因中常见遗传变异对胆道癌和结石风险的影响(411 例癌症病例、895 例结石病例和 786 例对照)。我们对 6 个单核苷酸多态性(SNP)进行了基因分型,其中 4 个位于 ESR1(rs2234693、rs3841686、rs2228480 和 rs1801132),2 个位于 ESR2(rs1256049 和 rs4986938)。在所有参与者中,ESR1 rs1801132(P325P)G 等位基因与胆管[比值比(OR)=1.7,95%置信区间(CI)1.1-2.8]和 Vater 壶腹癌(OR=2.1,95%CI 0.9-4.9)的风险增加有关与 CC 基因型相比。该关联在男性中(OR=2.8,95%CI 1.4-5.7)而非女性中明显(P 异质性=0.01)。此外,与 AA 基因型相比,ESR2 rs4986938(3'STP 处的 38 bp)GG 基因型与胆管癌的风险升高相关(OR=3.3,95%CI 1.3-8.7),尽管这一估计基于少数受试者。没有研究的其他 SNP 与胆道癌或结石相关。经过错误发现率调整的 P 值不显著(P>0.1)。基于四个 SNP 的 ESR1 单倍型未发现关联。这些初步结果表明,ESR 基因中的变异可能在胆道癌的病因学中发挥作用,尤其是男性的胆管癌。