Vishnoi Monika, Pandey Sachchida Nand, Modi Dinesh Raj, Kumar Ashok, Mittal Balraj
Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow 226014, India.
Hum Immunol. 2008 Jun;69(6):360-7. doi: 10.1016/j.humimm.2008.04.004. Epub 2008 May 6.
Epidermal growth factor (EGF) and transforming growth factor beta1 (TGFbeta1) play important roles in tumor biology. Single nucleotide polymorphisms in EGF and TGFB1 genes alter the expression of these growth factors and influence the tumorigenesis process. The aim of our present study was to determine the association of EGF+61A>G (rs4444903) and TGFB1-509C>T (rs1800469) gene polymorphism with susceptibility to gallbladder cancer (GBC). The present case-control association study was carried out in 126 confirmed GBC patients and 190 healthy subjects. Genotyping was performed by polymerase chain reaction-restriction fragment length polymorphism methods. The GG genotype of EGF+61A>G was significantly associated with GBC [p=0.012, odds ratio (OR)=2.22, 95% confidence interval (CI)=1.19-4.15] in comparison to healthy subjects. Analysis based on gender indicated risk due to GG genotype was limited to female GBC patients (p=0.003, OR=3.45, 95% CI=1.52-7.82). Upon stratification of GBC patients on the basis of the presence or absence of gallstones, the risk due to EGF polymorphism was not modulated by the status of gallstones. The TGFB1-509C>T polymorphism was not associated with GBC. Also, we did not find any association of this polymorphism when GBC patients were subdivided on the basis of gender. However, after stratification of GBC patients on the status of gallstones, we determined that the CT genotype of TGFB1 was associated with increased risk of GBC without gallstones (p value=0.030, OR=2.90, 95% CI=1.26-6.69). Furthermore, the combination of the GG genotype of EGF and the CT genotype of TGFB1 demonstrated synergistic increase in risk of GBC. In conclusion, the higher producing +61G allele of EGF and -509 CT genotype of TGFB1 synergistically increase the susceptibility of gallbladder cancer (p value=0.003). Further study in large samples size is required to confirm our findings.
表皮生长因子(EGF)和转化生长因子β1(TGFβ1)在肿瘤生物学中发挥着重要作用。EGF和TGFB1基因中的单核苷酸多态性会改变这些生长因子的表达,并影响肿瘤发生过程。我们当前研究的目的是确定EGF+61A>G(rs4444903)和TGFB1-509C>T(rs1800469)基因多态性与胆囊癌(GBC)易感性之间的关联。本病例对照关联研究在126例确诊的GBC患者和190名健康受试者中进行。通过聚合酶链反应-限制性片段长度多态性方法进行基因分型。与健康受试者相比,EGF+61A>G的GG基因型与GBC显著相关[p=0.012,比值比(OR)=2.22,95%置信区间(CI)=1.19-4.15]。基于性别的分析表明,GG基因型导致的风险仅限于女性GBC患者(p=0.003,OR=3.45,95%CI=1.52-7.82)。根据GBC患者是否存在胆结石进行分层后,EGF多态性导致的风险不受胆结石状态的调节。TGFB1-509C>T多态性与GBC无关。此外,当根据性别对GBC患者进行细分时,我们未发现该多态性存在任何关联。然而,在根据胆结石状态对GBC患者进行分层后,我们确定TGFB1的CT基因型与无胆结石的GBC风险增加相关(p值=0.030,OR=2.90,95%CI=1.26-6.69)。此外,EGF的GG基因型和TGFB1的CT基因型组合显示GBC风险协同增加。总之,EGF产生较高水平的+61G等位基因和TGFB1的-509 CT基因型协同增加胆囊癌易感性(p值=0.003)。需要进一步进行大样本量研究以证实我们的发现。