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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Prognostic and clinicopathologic significance of long non-coding RNA opa-interacting protein 5-antisense RNA 1 in multiple human cancers
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Prognostic and clinicopathologic significance of long non-coding RNA opa-interacting protein 5-antisense RNA 1 in multiple human cancers

机译:多重非编码RNA OPA相互作用蛋白5-反义RNA 1在多个人类癌症中的预后和临床病理学意义

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div class="hlFld-Abstract test" Background: OIP5-AS1 has been reported to be aberrantly expressed in multiple cancers and associated with clinical outcomes. We conducted this study to assess the generalized prognostic value of OIP5-AS1 in cancers. Methods: PubMed, Web of science, and Cochrane Library were searched for eligible studies. Hazards ratios (HRs) or odd ratios (ORs) with 95% confidence intervals (CIs) were pooled to estimate the prognostic value of OIP5-AS1 in cancers, including overall survival (OS), age, gender, tumor size, clinical stage, and lymph node metastasis (LNM). Publication bias was measured by Begg’s test and funnel plot. Sensitivity analysis were used to detect the stability of pooled results. Results: Overall, eleven studies containing 713 patients were eventually enrolled. The pooled results showed that high OIP5-AS1 expression was correlated with shorter OS (HR?=?0.48, 95%CI: 0.35–0.64), regardless of the sample size, tumor type and follow-up time. Furthermore, elevated expression of OIP5-AS1 indicated advanced clinical stage (OR?=?2.12, 95% CI: 1.06–4.23), but not associated with age, gender, tumor size and LNM. No publication bias was detected. Conclusion: High expression of lncRNA OIP5-AS1 may predict a poor OS and advanced clinical stage, implicating that OIP5-AS1 may be a possible prognostic factor in cancers.
机译:Div类=“HLFLD-Abstract Test”>背景:据报道,OIP5-AS1在多种癌症中异常表达并与临床结果相关联。我们进行了该研究,以评估OIP5-AS1在癌症中的广义预后价值。方法:搜查了符合条件的研究的PubMed,科学网和Cochrane图书馆。合并危害比率(HRS)或奇数比率(或奇数比例(或者)汇总了95%置信区间(CIS)以估计OIP5-AS1在癌症中的预后值,包括整体存活(OS),年龄,性别,肿瘤大小,临床阶段,和淋巴结转移(LNM)。通过Begg的测试和漏斗图测量出版物偏差。敏感性分析用于检测合并结果的稳定性。结果:总体而言,含有713名患者的11项研究最终纳入。汇总结果表明,高OIP5-AS1表达与较短的OS(HR?= 0.48,95%CI:0.35-0.64)相关,无论样品大小,肿瘤类型和随访时间。此外,OIP5-AS1的升高表达显示了晚期临床阶段(或?=?2.12,95%CI:1.06-4.23),但与年龄,性别,肿瘤大小和LNM无关。没有检测到出版物偏见。结论:LNCRNA OIP5-AS1的高表达可以预测缺乏OS和晚期临床阶段,含有OIP5-AS1可能是癌症中可能的预后因素。

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