Vavilov Institute of General Genetics, Russian Academy of Sciences.
Acta Naturae. 2010 Oct;2(4):58-65.
This study presents the results of research on DNA polymorphism in children with malignant brain tumors (172 patients, 183 in the control group). Genotyping was performed using an allele-specific tetraprimer reaction for the genes of the first (CYP1A1 (2 sites)) and second phases of xenobiotic detoxication (GSTM1, GSTT1, GSTP1, GSTM3), DNA repair genesXRCC1, XPD(2 sites),OGG1, as well asNOS1andMTHFR.The increased risk of disease is associated with a minor variant ofCYP1A1(606G) (p = 0.009; OR = 1.50) and a deletion variant ofGSTT1, (p = 0.013, OR = 1.96). Maximum disease risk was observed in carriers of double deletions inGSTT1-GSTM1(p = 0.017, OR = 2.42). The obtained results are discussed in reference to literary data on the risk of malignant brain tumor formation in children and adults.
本研究报告了对儿童恶性脑肿瘤(172 例患者,对照组 183 例)DNA 多态性的研究结果。使用等位基因特异性四引物反应对第一阶段(CYP1A1(2 个位点))和第二阶段的外源解毒(GSTM1、GSTT1、GSTP1、GSTM3)、DNA 修复基因 XRCC1、XPD(2 个位点)、OGG1 以及 NOS1 和 MTHFR 的基因进行基因分型。CYP1A1(606G)(p = 0.009;OR = 1.50)和 GSTT1 缺失变体(p = 0.013,OR = 1.96)的较小变体与疾病风险增加相关。在 GSTT1-GSTM1 双重缺失的携带者中观察到最大的疾病风险(p = 0.017,OR = 2.42)。根据关于儿童和成人恶性脑肿瘤形成风险的文献数据,对获得的结果进行了讨论。