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Genetic Studies of a Cluster of Acute Lymphoblastic Leukemia Cases in Churchill County,Nevada

机译:内华达州丘吉尔县一组急性淋巴细胞白血病病例的遗传研究

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OBJECTIVE: In a study to identify exposures associated with 15 cases of childhood leukemia,we found levels of tungsten,arsenic,and dichlorodiphenyldichloroethylene in participants to be higher than mean values reported in the National Report on Human Exposure to Environmental Chemicals.Because case and comparison families had similar levels of these contaminants,we conducted genetic studies to identify gene polymorphisms that might have made case children more susceptible than comparison children to effects of the exposures.DESIGN: We compared case with comparison children to determine whether differences existed in the frequency of polymorphic genes,including genes that code for enzymes in the folate and purine pathways.We also included discovery of polymorphic forms of genes that code for enzymes that are inhibited by tungsten: xanthine dehydrogenase,sulfite oxidase (SUOX gene),and aldehyde oxidase.PARTICIPANTS: Eleven case children were age- and sex-matched with 42 community comparison children for genetic analyses.Twenty parents of case children also contributed to the analyses.RESULTS: One bilalleleic gene locus in SUOX was significantly associated with either case or comparison status,depending on which alleles the child carried (without adjusting for multiple comparisons).CONCLUSIONS: Although genetic studies did not provide evidence that a common agent or genetic susceptibility factor caused the leukemias,the association between a SUOX gene locus and disease status in the presence of high tungsten and arsenic levels warrants further investigation.RELEVANCE: Although analyses of community clusters of cancer have rarely identified causes,these findings have generated hypotheses to be tested in subsequent studies.
机译:目的:在一项研究中发现与15例儿童白血病有关的暴露量的研究中,我们发现参与者中的钨,砷和二氯二苯基二氯乙烯含量高于《国家人类环境化学物报告》中报告的平均值。家庭中这些污染物的水平相似,我们进行了基因研究,以找出可能使案例儿童比对比儿童更容易受到暴露影响的基因多态性。设计:我们将案例与对比儿童进行比较,以确定是否存在差异。多态性基因,包括在叶酸和嘌呤途径中编码酶的基因。我们还发现了多态性形式的基因,该基因编码受钨抑制的酶:黄嘌呤脱氢酶,亚硫酸盐氧化酶(SUOX基因)和醛氧化酶。 :11名儿童的年龄和性别相匹配,有42个社区比较结果:SUOX中的一个双歧基因位点与病例或比较状态显着相关,这取决于孩子携带的等位基因(无需为多个比较进行调整)。结论:尽管遗传学研究没有提供证据表明一种共同的病因或遗传易感性因素导致了白血病,但是在高钨和高砷水平下,SUOX基因位点与疾病状态之间的关联值得进一步研究。相关性:尽管对社区进行了分析癌症群很少发现原因,这些发现产生了假设,需要在后续研究中进行检验。

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