Cong Lei, Wang Wei-bo, Liu Qi, Du Jia-jun
Department of Oncology, Shandong Provincial Hospital Affiliated to Shandong University.
Tohoku J Exp Med. 2015 Jul;236(3):219-24. doi: 10.1620/tjem.236.219.
Vitamin D is a potential protective agent against cancer, and its activity is mediated mainly by vitamin D receptor (VDR). The FokI polymorphism (rs10735810) represents a T-to-C transition (ATG to ACG) in exon 2 of the VDR gene, and this ATG represents the translation-initiation codon, encoded by the f allele. The FokI polymorphism results in the generation of a protein shortened by three amino acids, translated from the downstream ATG codon (the F allele). We investigated the relationship between the FokI polymorphism and gastric cancer in a Chinese Han population. A total of 187 patients and 212 healthy controls were enrolled. The FokI polymorphism was detected by polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) analysis. The f allele frequency was higher in patients than that in controls (51.6% and 43.6%, P < 0.05). Multivariate logistics regression analysis revealed patients with the f allele (Ff + ff) showed a higher risk of gastric cancer [odds ratio (95% confidence interval) 2.73 (1.13~4.32)]. Patients with the f allele (Ff + ff) also presented a poorly differentiated type of gastric cancer (P < 0.05) and higher levels of C-reactive protein on admission than the FF group (5.5 ± 2.4 mg/L vs. 3.4 ± 1.3 mg/L, P < 0.05). Here, we show an association between the VDR FokI polymorphism and the susceptibility to gastric cancer, which may be helpful for early detection of high-risk individuals with the f allele for gastric cancer. Conversely, the F allele may be a protective factor against gastric cancer.
维生素D是一种潜在的抗癌保护剂,其活性主要由维生素D受体(VDR)介导。FokI多态性(rs10735810)代表VDR基因外显子2中的T到C转换(ATG到ACG),这个ATG代表翻译起始密码子,由f等位基因编码。FokI多态性导致从下游ATG密码子(F等位基因)翻译产生一种缩短了三个氨基酸的蛋白质。我们在中国汉族人群中研究了FokI多态性与胃癌之间的关系。共纳入187例患者和212例健康对照。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析检测FokI多态性。患者的f等位基因频率高于对照组(51.6%和43.6%,P<0.05)。多因素逻辑回归分析显示,携带f等位基因(Ff+ff)的患者患胃癌的风险更高[比值比(95%置信区间)2.73(1.13~4.32)]。携带f等位基因(Ff+ff)的患者还表现为低分化型胃癌(P<0.05),入院时C反应蛋白水平高于FF组(5.5±2.4mg/L对3.4±1.3mg/L,P<0.05)。在此,我们显示VDR FokI多态性与胃癌易感性之间存在关联,这可能有助于早期检测携带f等位基因的胃癌高危个体。相反,F等位基因可能是胃癌的一个保护因素。