首页> 外文期刊>Cellular and molecular biology >Investigation of some DNA repair genes association in non small cell lung cancer
【24h】

Investigation of some DNA repair genes association in non small cell lung cancer

机译:非小细胞肺癌中某些DNA修复基因的关联研究

获取原文
获取原文并翻译 | 示例
           

摘要

Ribonucleoside-diphosphate reductase subunit M2, also known as ribonucleotide reductase small subunit, is an enzyme that in humans is encoded by the RRM2 gene and also Ribonucleoside-diphosphate reductase large subunit is an enzyme that in humans is encoded by the RRM1 gene. RRM1 is a gene important in determining tumor phenotype, but also induced the expression of PTEN tumor suppressor gene, cell migration, invasion and metastasis formation, and play a preventive role. ERCC2 DNA repair mechanism is associated in more than 20 genes involved in the NER pathway. The aim of this study is to investigate rs13181 ERCC2 (T>G) (Lys751Gln), rs12806698 RRM1 (-269C>A) and rs6759180 (located in the 5'UTR) RRM2 (10126436G>A) gene polymorphisms by using real time PCR technique in patients with NSCLC. 193 NSCLC cases and 141 healthy control cases were included in this study. A significant difference was found between rs12806698 RRM1 genotype distributions (*p: 0.034) and were determined increases the risk of disease approximately 3.044 times AA genotype having (*p: 0.014 OR: 3.044, 95% CI: 1.205-7,688). A significant difference was found between rs6759180 RRM2 genotype distributions (*p: 0.033) and were determined increases the risk of disease approximately 3.49 times GG genotype having (p: 0,009 OR: 3, 49, % 95CI: 1.291-9,482). It was found significant difference in serum 8-OHdG levels between patients and controls (*p: 0001).
机译:核糖核苷二磷酸还原酶亚基M2,也称为核糖核苷酸还原酶小亚基,是一种在人类中由RRM2基因编码的酶,核糖核苷二磷酸还原酶大亚基也是在人中由RRM1基因编码的酶。 RRM1是决定肿瘤表型的重要基因,还诱导PTEN抑癌基因的表达,细胞迁移,侵袭和转移形成,并起到预防作用。 ERCC2 DNA修复机制与NER通路中涉及的20多个基因相关。本研究的目的是通过实时PCR研究rs13181 ERCC2(T> G)(Lys751Gln),rs12806698 RRM1(-269C> A)和rs6759180(位于5'UTR)RRM2(10126436G> A)基因多态性。 NSCLC患者的手术技巧。这项研究包括193例NSCLC病例和141例健康对照病例。发现rs12806698 RRM1基因型分布之间存在显着差异(* p:0.034),并确定该疾病风险增加了AA基因型(* p:0.014或:3.044,95%CI:1.205-7,688)的3.044倍。发现rs6759180 RRM2基因型分布之间存在显着差异(* p:0.033),并且确定该疾病风险增加了GG基因型(p:0,009或:3,49,%95CI:1.291-9,482)的3.49倍。发现患者和对照组之间的血清8-OHdG水平存在显着差异(* p:0001)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号