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长链非编码 RNA uc.338 的上调预示着非小细胞肺癌患者的预后不良。

Up-regulation of long noncoding RNA uc.338 predicts poor survival in non-small cell lung cancer.

出版信息

Cancer Biomark. 2018;22(4):781-785. doi: 10.3233/CBM-181331.

Abstract

BACKGROUND

Long noncoding RNA ultraconserved element 338 (uc.338) is a long non-coding RNA reported to function as a promoter in non-small cell lung cancer (NSCLC). However, the function and potential mechanism of uc.338 in NSCLC is still unclear.

OBJECTIVE

The aim of the present study was to assess the effect of uc.338 on the prognosis of patients with NSCLC.

METHODS

The expression levels of uc.338 in NSCLC tissues and matched normal lung tissues were examined by real-time quantitative PCR. Then the association between uc.338 levels with clinical variables as well as survival time was investigated.

RESULTS

We found that uc.338 expression levels were significantly upregulated in NSCLC compared with the matched noncancerous lung tissues (P< 0.01). In addition, increased uc.338 expression was significantly associated with TNM stage (P< 0.003), lymph node metastasis (P< 0.006) and distant metastasis (P< 0.002). More importantly, Kaplan-Meier survival analysis demonstrated that higher uc.338 expression levels were associated with a shorter overall survival (P< 0.0016) and disease-free survival (p< 0.0001) in NSCLC patients. Finally, univariate and multivariate Cox regression analyses revealed that uc.338 was an independent risk factor for overall survival and disease-free survival.

CONCLUSIONS

Our results show that uc.338 may play an important role in tumorigenesis and progression and could serve as a potential independent prognostic biomarker for patients with NSCLC.

摘要

背景

长链非编码 RNA 超保守元件 338(uc.338)是一种长链非编码 RNA,据报道在非小细胞肺癌(NSCLC)中作为启动子发挥作用。然而,uc.338 在 NSCLC 中的功能和潜在机制尚不清楚。

目的

本研究旨在评估 uc.338 对 NSCLC 患者预后的影响。

方法

采用实时定量 PCR 检测 NSCLC 组织和配对正常肺组织中 uc.338 的表达水平。然后,研究了 uc.338 水平与临床变量和生存时间之间的关系。

结果

我们发现,uc.338 在 NSCLC 中的表达水平明显高于配对的非癌性肺组织(P<0.01)。此外,uc.338 表达水平的升高与 TNM 分期(P<0.003)、淋巴结转移(P<0.006)和远处转移(P<0.002)显著相关。更为重要的是,Kaplan-Meier 生存分析表明,uc.338 表达水平较高的 NSCLC 患者总生存期(P<0.0016)和无病生存期(p<0.0001)较短。最后,单因素和多因素 Cox 回归分析显示,uc.338 是总生存期和无病生存期的独立危险因素。

结论

我们的研究结果表明,uc.338 可能在肿瘤发生和进展中发挥重要作用,并可能成为 NSCLC 患者潜在的独立预后生物标志物。

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