Dai Liping, Gast Andreas, Horska Alexandra, Schrappe Martin, Bartram Claus R, Hemminki Kari, Kumar Rajiv, Bermejo Justo Lorenzo
Division of Molecular Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Pediatr Blood Cancer. 2009 Jul;52(7):819-23. doi: 10.1002/pbc.21971.
Inherited genetic variants in critical genes can putatively modulate susceptibility to childhood acute lymphoblastic leukemia (ALL).
We used allelic discrimination method to genotype 19 polymorphisms in the transforming growth factor-beta1 (TGF-beta1), transforming growth factor-beta receptor 1 (TGF-betaR1) and transforming growth factor-beta receptor 2 (TGF-betaR2) genes in 460 cases of childhood acute ALL and 552 ethnically matched controls. The genotyped polymorphisms included functional and tagging variants to cover the three genes in entirety. We used multidimensionality reduction (MDR) method to test effect of multiple genes on disease susceptibility. In order to increase statistical power and detect susceptibility variants not directly genotyped in this study, we used imputation using HapMap data.
None of the genotyped polymorphisms or the consequent haplotypes showed any association with risk modulation. The results, however, did show a marginal association (odds ratio OR 0.76, 95% confidence interval CI 0.59-0.97) of the variant allele for the rs10417924 polymorphism located at 3'untranslated region of the TGF-beta1 gene with the B-cell lineage ALL. No other polymorphism showed any association with childhood ALL susceptibility. A signal of marginal significance for the rs10417924 polymorphism in the TGF-beta1 gene in B-cell lineage ALL showed up with both MDR and imputation techniques.
These data rule out the role of polymorphisms in the TGF-beta1, TGF-betaR1 and TGF-betaR2 genes in susceptibility to childhood ALL. However, for B-lineage ALL, the role of the rs10417924 polymorphism in TGF-beta1 gene needs further investigation.
关键基因中的遗传变异可能会调节儿童急性淋巴细胞白血病(ALL)的易感性。
我们采用等位基因鉴别法,对460例儿童急性淋巴细胞白血病患者和552例种族匹配的对照者的转化生长因子β1(TGF-β1)、转化生长因子β受体1(TGF-βR1)和转化生长因子β受体2(TGF-βR2)基因中的19个多态性位点进行基因分型。所分型的多态性位点包括功能性和标签性变异,以全面覆盖这三个基因。我们使用多维度约简(MDR)方法来测试多个基因对疾病易感性的影响。为了提高统计效能并检测本研究中未直接进行基因分型的易感变异,我们使用HapMap数据进行了插补分析。
所分型的多态性位点或由此产生的单倍型均未显示出与风险调节有任何关联。然而,结果确实显示位于TGF-β1基因3'非翻译区的rs10417924多态性位点的变异等位基因与B细胞系ALL存在边缘关联(优势比OR 0.76,95%置信区间CI 0.59 - 0.97)。没有其他多态性位点显示出与儿童ALL易感性有任何关联。TGF-β1基因中rs10417924多态性位点在B细胞系ALL中的边缘显著信号在MDR和插补技术中均出现。
这些数据排除了TGF-β1、TGF-βR1和TGF-βR2基因中的多态性位点在儿童ALL易感性中的作用。然而,对于B系ALL,TGF-β1基因中rs10417924多态性位点的作用需要进一步研究。