首页> 外文期刊>Oncology reports >Genetic polymorphisms in the DNA repair genes XPD and XRCC1, p53 gene mutations and bladder cancer risk.
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Genetic polymorphisms in the DNA repair genes XPD and XRCC1, p53 gene mutations and bladder cancer risk.

机译:DNA修复基因XPD和XRCC1,p53基因突变和膀胱癌风险中的遗传多态性。

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摘要

Previous studies have suggested that certain genetic polymorphisms, specifically the Xeroderma pigmentosum group D (XPD) gene codon 751 and the X-ray repair cross-complementing group 1 (XRCC1) gene codon 399 polymorphisms, were associated with an increased risk of lung cancer, and, in some studies, with a greater risk for mutations in the p53 tumor suppressor gene in lung tumors. To evaluate whether these gene polymorphisms may be associated with an increased risk for bladder cancer or in association with p53 mutation status in bladder tumors, we screened for polymorphisms at XPD codons 751 and XRCC1 codon 399 in DNA isolated from blood of 194 bladder cancer patients and 313 healthy controls and for mutations in exons 4 to 8 of the p53 gene in bladder tumor DNA from 174 bladder cancer patients. There was a significantly higher prevalence of the XPD 751 Gln allele among the bladder cancer group, compared with the control group. No association was found between bladder cancer risk and the XRCC1 399 polymorphism. p53 mutations were found in 20.1% (35/174) patients. There was no difference in p53 mutation status among individuals with different genotypes. These results suggest that individuals who have the XPD 751 Gln allele may be at an increased risk for bladder cancer, although this may not lead to an increased risk for mutations in the p53 gene.
机译:先前的研究表明,某些遗传多态性,特别是色素干性皮肤病D组(XPD)基因密码子751和X射线修复交叉互补第1组(XRCC1)基因密码子399基因多态性,与罹患肺癌的风险增加相关,并且在某些研究中,肺肿瘤中p53抑癌基因突变的风险更大。为了评估这些基因多态性是否可能与膀胱癌的风险增加或与膀胱肿瘤中的p53突变状态有关,我们从194例膀胱癌患者血液中分离的DNA中筛选了XPD密码子751和XRCC1密码子399处的多态性。 313名健康对照者和来自174名膀胱癌患者的膀胱肿瘤DNA中p53基因外显子4至8的突变。与对照组相比,膀胱癌组中XPD 751 Gln等位基因的患病率明显更高。在膀胱癌风险与XRCC1 399基因多态性之间未发现关联。在20.1%(35/174)的患者中发现了p53突变。在不同基因型个体之间,p53突变状态没有差异。这些结果表明,具有XPD 751 Gln等位基因的个体患膀胱癌的风险可能增加,尽管这可能不会导致p53基因突变的风险增加。

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