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胸苷酸合成酶启动子和 DNA 修复基因多态性对儿童急性淋巴细胞白血病易感性的影响。

Impact of thymidylate synthase promoter and DNA repair gene polymorphisms on susceptibility to childhood acute lymphoblastic leukemia.

机构信息

Colegiado de Biomedicina, Campus Ministro Reis Velloso, Universidade Federal do Piauí, Parnaíba, Piauí, Brazil.

出版信息

Leuk Lymphoma. 2011 Jun;52(6):1118-26. doi: 10.3109/10428194.2011.559672. Epub 2011 Apr 4.

Abstract

The aim of this study was to evaluate the frequency of polymorphisms in the TYMS, XRCC1, and ERCC2 DNA repair genes in pediatric patients with acute lymphoblastic leukemia using polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism (RFLP) approaches. The study was conducted in 206 patients and 364 controls from a Brazilian population. No significant differences were observed among the analyzed groups regarding XRCC1 codon 399 and codon 194 and ERCC2 codon 751 and codon 312 polymorphisms. The TYMS 3R variant allele was significantly associated with a reduced risk of childhood ALL, represented by the sum of heterozygous and polymorphic homozygous genotypes (odds ratio 0.60; 95% confidence interval 0.37-0.99). The results suggest that polymorphism in TYMS may play a protective role against the development of childhood ALL.

摘要

本研究旨在采用聚合酶链反应(PCR)和 PCR-限制性片段长度多态性(RFLP)方法评估儿童急性淋巴细胞白血病患者 TYMS、XRCC1 和 ERCC2 基因中 DNA 修复基因多态性的频率。该研究在来自巴西人群的 206 名患者和 364 名对照中进行。在分析的各组之间,XRCC1 密码子 399 和密码子 194 以及 ERCC2 密码子 751 和密码子 312 多态性无显著差异。TYMS 3R 变异等位基因与儿童 ALL 风险降低显著相关,其表现为杂合子和多态性纯合子基因型的总和(比值比 0.60;95%置信区间 0.37-0.99)。结果表明,TYMS 多态性可能对儿童 ALL 的发生起保护作用。

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