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首页> 外文期刊>Annals of epidemiology >#21-S the role of MDR-1 gene polymorphisms in the genetic susceptibility to childhood leukemia.
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#21-S the role of MDR-1 gene polymorphisms in the genetic susceptibility to childhood leukemia.

机译:#21-S MDR-1基因多态性在儿童白血病遗传易感性中的作用。

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PURPOSE: Childhood leukemia is likely a multifaceted disease resulting from a combination of environmental and genetic factors. P-glycoprotein (PGP), encoded by the MDR-1 gene, is a transmembrane protein that serves as an efflux pump for a wide variety of lipophilic compounds and has a physiologic role of protecting cells against the DNA damaging potential of certain xenobiotics. The polymorphism, C3435T, of this gene has been correlated with altered PGP function in the cells of the intestine, placenta, and hematological compartments. Therefore, we question the putative role of MDR-1 polymorphisms as a susceptibility factor of childhood leukemia.METHODS: Buccal cell DNA of 151 pediatric leukemia cases and 193 control children ascertained through the Northern California Childhood Leukemia Study were genotyped for two common MDR-1 gene polymorphisms, C1236T and C3435T. Genotype data was obtained using multiplex polymerase chain reaction and single nucleotide polymorphism analysis that utilizes the single base extension procedure.RESULTS: Overall allele frequencies of C1236T (45%) and C3435T (49%) were comparable to allele frequencies reported in other studies. Children with the C3435T variant allele were not at a significantly increased risk of developing leukemia. The association between C1236T and leukemia was not statistically significant but was suggestive of a dose response effect. A stratified analysis showed no evidence that C1236T and C3435T affect risk of childhood leukemia differently between Hispanic and non-Hispanic White populations. Limiting the population to acute lymphoblastic leukemia yielded similar results.CONCLUSION: Results of this study provide little evidence that MDR-1 gene polymorphisms alone significantly affect risk of childhood leukemia. Further evaluation, in the context of gene-gene and gene-environment interactions, is required before definitive conclusions are made regarding the role of the MDR-1 gene in the susceptibility to childhood leukemia.
机译:目的:儿童白血病可能是环境和遗传因素共同作用的多方面疾病。由MDR-1基因编码的P-糖蛋白(PGP)是一种跨膜蛋白,可作为多种亲脂性化合物的外排泵,并具有保护细胞免受某些异质生物的DNA破坏潜能的生理作用。该基因的多态性C3435T与肠道,胎盘和血液室的PGP功能改变有关。因此,我们质疑MDR-1多态性作为儿童白血病易感性因素的假定作用。方法:对通过北加州儿童白血病研究确定的151例小儿白血病病例和193例对照儿童的颊细胞DNA进行了基因分型,以分析两种常见的MDR-1基因多态性,C1236T和C3435T。通过多重聚合酶链反应和利用单碱基延伸程序的单核苷酸多态性分析获得基因型数据。结果:C1236T(45%)和C3435T(49%)的总等位基因频率与其他研究报告的等位基因频率相当。具有C3435T变异等位基因的儿童患白血病的风险没有显着增加。 C1236T与白血病之间的相关性在统计学上不显着,但暗示剂量反应作用。分层分析显示,没有证据表明C1236T和C3435T对西班牙裔和非西班牙裔白人人群影响儿童白血病的风险有所不同。将人群限制为急性淋巴细胞白血病也得到了类似的结果。结论:这项研究的结果几乎没有证据表明MDR-1基因多态性单独显着影响儿童白血病的风险。在就MDR-1基因在儿童白血病易感性中的作用做出明确结论之前,需要在基因-基因和基因-环境相互作用的背景下进行进一步评估。

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