首页> 美国卫生研究院文献>Oncotarget >Long non-coding RNA XIST as a potential prognostic biomarker in human cancers: a meta-analysis
【2h】

Long non-coding RNA XIST as a potential prognostic biomarker in human cancers: a meta-analysis

机译:长非编码RNA XIST作为人类癌症的潜在预后生物标志物:一项荟萃分析

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

Growing studies have confirmed that long non-coding RNAs (lncRNAs) involve in the occurrence and development of various cancers. XIST, as a lncRNA, was dysregulated in different cancers. This meta-analysis was performed to evaluate the prognostic potential of XIST in malignant tumors. Eight databases of PubMed, Web of Science, Embase, Cochrane library, CNKI, VIP, SinoMed and Wang Fang were comprehensively searched from their initiation date to August 15, 2017. A total of nine studies with 853 cancer patients met the including criteria were finally included in this meta-analysis after independently screening the literatures by two researchers. Any discrepancies were resolved by a consensus. Hazard ratios (HRs) with corresponding 95% confidence intervals (CIs) for the primary endpoints were extracted and pooled for meta-analysis. Our results showed that expression level of XIST was markedly associated with overall survival (function as oncogene, HR = 0.53, 95% CI: 0.42–0.68, p < 0.00001; function as tumor suppressor, HR = 2.25, 95% CI: 1.15–4.37, p = 0.02), disease free survival (DFS)(HR = 0.45; 95% CI: 0.31–0.67, p < 0.0001), tumor type (digestive system carcinoma, HR = 0.50; 95% CI: 0.37–0.69, p < 0.00001; non-digestive system carcinoma, HR = 0.58; 95% CI: 0.39–0.87, p = 0.008), lymph node metastasis (OR = 0.32, 95% CI: 0.20–0.52, p < 0.00001), distant metastasis (OR = 0.36, 95% CI: 0.22–0.60, p < 0.0001) and tumor stage (OR = 0.43, 95% CI: 0.31–0.60, p < 0.00001). In conclusion, the pooled results in our current work suggest that XIST is an important prognostic biomarker in cancer patients.
机译:越来越多的研究证实,长的非编码RNA(lncRNA)参与了各种癌症的发生和发展。 XIST作为lncRNA,在不同的癌症中均失调。进行这项荟萃分析,以评估XIST在恶性肿瘤中的预后潜力。从启动日期到2017年8月15日,共检索了PubMed,Web of Science,Embase,Cochrane图书馆,CNKI,VIP,SinoMed和Wang Fang的八个数据库。共对9项涉及853名癌症患者的研究进行了最终纳入标准在由两名研究人员独立筛选文献后,本荟萃分析中纳入了本文。任何差异均通过协商一致解决。提取主要终点的危险比(HRs)和相应的95%置信区间(CIs),并将其合并以进行荟萃分析。我们的结果表明,XIST的表达水平与总体存活率显着相关(起癌基因作用,HR = 0.53,95%CI:0.42-0.68,p <0.00001;起肿瘤抑制作用,HR = 2.25,95%CI:1.15- 4.37,p = 0.02),无病生存期(DFS)(HR = 0.45; 95%CI:0.31-0.67,p <0.0001),肿瘤类型(消化系统癌,HR = 0.50; 95%CI:0.37-0.69, p <0.00001;非消化系统癌,HR = 0.58; 95%CI:0.39–0.87,p = 0.008),淋巴结转移(OR = 0.32,95%CI:0.20–0.52,p <0.00001),远处转移(OR = 0.36,95%CI:0.22-0.60,p <0.0001)和肿瘤分期(OR = 0.43,95%CI:0.31-0.60,p <0.00001)。总之,我们当前工作中的汇总结果表明,XIST是癌症患者中重要的预后生物标志物。

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