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Expression of Selenoprotein Genes and Association with Selenium Status in Colorectal Adenoma and Colorectal Cancer

机译:硒蛋白基因的表达与结直肠腺瘤和结直肠癌的硒状况

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摘要

Dietary selenium (Se) intake is essential for synthesizing selenoproteins that are important in countering oxidative and inflammatory processes linked to colorectal carcinogenesis. However, there is limited knowledge on the selenoprotein expression in colorectal adenoma (CRA) and colorectal cancer (CRC) patients, or the interaction with Se status levels. We studied the expression of seventeen Se pathway genes (including fifteen of the twenty-five human selenoproteins) in RNA extracted from disease-normal colorectal tissue pairs, in the discovery phase of sixty-two CRA/CRC patients from Ireland and a validation cohort of a hundred and five CRC patients from the Czech Republic. Differences in transcript levels between the disease and paired control mucosa were assessed by the Mann-Whitney U-test. GPX2 and TXNRD3 showed a higher expression and GPX3, SELENOP, SELENOS, and SEPHS2 exhibited a lower expression in the disease tissue from adenomas and both cancer groups (p-values from 0.023 to <0.001). In the Czech cohort, up-regulation of GPX1, SELENOH, and SOD2 and down-regulation of SELENBP1, SELENON, and SELENOK (p-values 0.036 to <0.001) was also observed. We further examined the correlation of gene expression with serum Se status (assessed by Se and selenoprotein P, SELENOP) in the Irish patients. While there were no significant correlations with both Se status markers, SELENOF, SELENOK, and TXNRD1 tumor tissue expression positively correlated with Se, while TXNRD2 and TXNRD3 negatively correlated with SELENOP. In an analysis restricted to the larger Czech CRC patient cohort, Cox regression showed no major association of transcript levels with patient survival, except for an association of higher SELENOF gene expression with both a lower disease-free and overall survival. Several selenoproteins were differentially expressed in the disease tissue compared to the normal tissue of both CRA and CRC patients. Altered selenoprotein expression may serve as a marker of functional Se status and colorectal adenoma to cancer progression.
机译:膳食硒(Se)的摄入量是用于合成是在打击氧化和连接至结直肠癌发生的炎症过程重要硒蛋白是必不可少的。然而,在大肠腺瘤(CRA)的硒蛋白表达有限的知识和结直肠癌(CRC)的患者,或硒状态级别的交互。我们研究的17个硒途径基因(包括25人硒蛋白15)中RNA表达从疾病正常结直肠组织对萃取,在从爱尔兰62 CRA / CRC患者发现阶段和的验证队列一百零五CRC患者来自捷克共和国。在疾病和配对控制粘膜之间的转录水平的差异通过曼 - 惠特尼U检验进行评估。 GPX2和TXNRD3表现出较高的表达和GPX3,SELENOP,SELENOS和SEPHS2表现出从腺瘤和癌两者组(p值从0.023至<0.001)疾病组织更低的表达。在捷克队列,GPX1,SELENOH的上调,和SOD2和SELENBP1,SELENON的下调,和SELENOK(p值0.036至<0.001),也观察到。我们进一步研究的基因表达的相关性与血清硒状态在爱尔兰的患者(由Se和硒蛋白P,SELENOP评估)。虽然有与两个硒状态标记没有显著相关性,SELENOF,SELENOK和TXNRD1肿瘤组织中的表达正相关硒相关,而TXNRD2和TXNRD3负SELENOP相关。在限制较大捷克CRC患者队列的分析,Cox回归表明转录水平没有重大关联与病人的生存,除了较高的SELENOF基因表达的同时具有较低的无病生存率和总生存率的关联。几个硒蛋白进行了比较,两者CRA和CRC患者的正常组织在疾病组织差异表达。改变的硒蛋白表达可作为功能性硒状态和结肠直肠腺瘤到癌的进展的标志物。

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