首页> 美国卫生研究院文献>Journal of Translational Medicine >Selenium-binding protein 1 transcriptionally activates p21 expression via p53-independent mechanism and its frequent reduction associates with poor prognosis in bladder cancer
【2h】

Selenium-binding protein 1 transcriptionally activates p21 expression via p53-independent mechanism and its frequent reduction associates with poor prognosis in bladder cancer

机译:硒结合蛋白1通过独立于p53的机制转录激活p21表达其频繁减少与膀胱癌的不良预后相关

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

SELENBP1 is frequently down-regulated in human bladder cancer, and low expression of SELENBP1 predicts poor clinical prognosis. Twelve pairs of bladder cancers (T) and adjacent matched normal tissues (N) were extracted and subjected to immunoblotting assay for determining the levels of SELENBP1 protein expression. GAPDH was used as a loading control. Relative intensity of SELENBP1 in was determined using Quantity One software, and normalized to GAPDH. The relative intensity of SELENBP1 in normal tissues was set to 1.0. Paired t test was performed and value was indicated in top panel. mRNA levels were extracted from TCGA bladder cancer (TCGA-BLCA) cohort, including 19 of normal bladder tissues and 406 of bladder cancer tissues. Non-paired t test was performed and value was indicated in the panel. Kaplan–Meier 10-year survival analysis among patients with high and low expression in TCGA-BLCA cohort. The log-rank test was performed and value was indicated in the panel. Hazard ration (HR) and 95% confidence interval (CI) were also calculated
机译:SELENBP1在人类膀胱癌中经常被下调,而SELENBP1的低表达预示了不良的临床预后。提取十二对膀胱癌(T)和相邻的匹配的正常组织(N),并进行免疫印迹测定以确定SELENBP1蛋白表达的水平。 GAPDH被用作上样对照。使用Quantity One软件确定SELENBP1的相对强度,并标准化为GAPDH。正常组织中SELENBP1的相对强度设置为1.0。进行配对t检验,并且在顶部面板中指示值。从TCGA膀胱癌(TCGA-BLCA)队列中提取mRNA水平,该队列包括19个正常膀胱组织和406个膀胱癌组织。进行了非配对的t检验,并在面板中指示了数值。在TCGA-BLCA队列中高表达和低表达的患者中进行Kaplan–Meier 10年生存分析。进行了对数秩检验,并在面板中指出了数值。还计算了危险比(HR)和95%置信区间(CI)

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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