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Genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukemia.

机译:遗传多态性和对儿童急性淋巴细胞白血病的易感性。

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Acute lymphoblastic leukemia (ALL) is the most common form of pediatric cancer. Although exposure to environmental agents appears to predispose individuals to this disease, little attention has been paid to the role of genetic susceptibility to environmental exposures in the etiology of childhood ALL. The enzymes GSTM1, GSTT1, GSTP1, CYP1A1, and CYP2E1 are involved in the bioactivation and detoxification of a variety of xenobiotics present in food, organic solvents, tobacco smoke, drugs, alcoholic drinks, pesticides, and environmental pollutants. Polymorphisms in the genes coding for these enzymes have been associated with increased susceptibility to different cancers, including hematologic malignancies. To investigate whether these polymorphisms represent risk-modifying factors for childhood ALL, a study was conducted involving 113 Brazilian patients of childhood ALL and 221 controls with similar ethnic backgrounds. The data revealed that carriers of the rare GSTP1 Val allele were at higher risk of ALL (odds ratio [OR] = 2.7; 95% confidence interval [CI] = 1.1-6.8; P = 0.04). No difference was found in the prevalence of the GSTM1 and GSTT1 null genotypes between ALL patients and the controls, and no association was found between CYP1A1*2 and CYP2E1*3 variants and ALL. However, when the mutant CYP1A1 and CYP2E1 alleles were considered together with the GSTM1 and GSTP1 risk-elevating genotypes, the risk of ALL was increased further (OR = 10.3; 95% CI = 1.0-111.8; P = 0.05), suggesting a combined effect. These results imply that genetic variants of xenobiotic metabolizing genes influence the risk of developing childhood ALL. Environ. Mol. Mutagen. 43:100-109, 2004.
机译:急性淋巴细胞白血病(ALL)是儿童癌症的最常见形式。尽管暴露于环境因素似乎使个体容易患此病,但很少关注遗传因素对环境暴露在儿童ALL病因中的作用。酶GSTM1,GSTT1,GSTP1,CYP1A1和CYP2E1参与食品,有机溶剂,烟草烟雾,药物,酒精饮料,农药和环境污染物中存在的多种异源生物的生物活化和解毒。编码这些酶的基因的多态性与对不同癌症(包括血液系统恶性肿瘤)的敏感性增加有关。为了调查这些多态性是否代表儿童ALL的风险改变因素,进行了一项研究,涉及113名巴西儿童ALL和221名具有相似种族背景的对照。数据显示,罕见的GSTP1 Val等位基因的携带者罹患ALL的风险更高(赔率[OR] = 2.7; 95%置信区间[CI] = 1.1-6.8; P = 0.04)。 ALL患者与对照组之间的GSTM1和GSTT1无效基因型的流行率没有差异,CYP1A1 * 2和CYP2E1 * 3变体与ALL之间也没有关联。但是,当将突变型CYP1A1和CYP2E1等位基因与GSTM1和GSTP1风险升高的基因型一起考虑时,ALL的风险进一步增加(OR = 10.3; 95%CI = 1.0-111.8; P = 0.05)影响。这些结果表明,异种代谢基因的遗传变异会影响儿童期ALL的发生风险。环境。大声笑诱变剂。 43:100-109,2004。

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