Zhan Bingxiang, Lu Dapeng, Luo Peng, Wang Baolong
Clin Lab. 2016 Nov 1;62(11):2203-2211. doi: 10.7754/Clin.Lab.2016.160426.
BACKGROUND: microRNAs are widely involved in a variety of life processes and considered as potential biomarkers of tumor prognosis. A growing number of studies have documented that miRNAs were associated with outcome in NSCLC patients and can act as a prognostic marker. However, existing studies concerning the relationship between miRNAs and outcome in NSCLC patients were contentious and dispersive. Therefore, a systematic metaanalysis to explore the prognostic value of miRNAs on NSCLC patients is urgently needed. METHODS: Electronic databases, including PubMed, EMBASE, and Web of Science were searched for all relevant articles. Only articles investigating the survival effect of microRNAs on NSCLC patients were included in this meta-analysis. Hazard ratios (HRs) with 95% confidence interval (CI) were extracted and pooled on overall survival (OS) and progression free survival (PFS)/disease-specific survival (DSS). RESULTS: 28 articles were finally included in the overall meta-analysis. The pooled results revealed that high expression miR-21 (HR = 2.82, 95% CI: 2.10 - 3.79), miR-200c (HR = 2.05, 95% CI: 1.36 - 3.07), and miR-125b (HR = 1.72, 95% CI: 1.30 - 2.28) were negatively associated with survival in NSCLC patients. Conversely, high expression miR-148b (HR = 0.37, 95% CI: 0.19 - 0.70), miR-365 (HR = 0.40, 95% CI: 0.27 - 0.59), miR-124 (HR = 0.29, 95% CI: 0.16 - 0.53), miR-32 (HR = 0.46, 95% CI: 0.33 - 0.65), miR-146a (HR = 0.35, 95% CI: 0.18 - 0.68), and miR-375 (HR = 0.66, 95% CI: 0.45 - 0.96) were significantly associated with better prognosis. Meanwhile, the expression of miR-93 (HR = 1.19, 95% CI: 0.38 - 3.69) and miR-126 (HR = 0.38, 95% CI: 0.12 - 1.16) showed no relationship with NSCLC prognosis. CONCLUSIONS: Our meta-analysis provided the evidence that miR-21, miR-200c, miR-125b, miR-148b, miR-365, miR-124, miR-32, miR-146a, and miR-375 can act as prognostic biomarkers in NSCLC.
背景:微小RNA广泛参与多种生命过程,被视为肿瘤预后的潜在生物标志物。越来越多的研究表明,微小RNA与非小细胞肺癌(NSCLC)患者的预后相关,并可作为预后标志物。然而,现有关于微小RNA与NSCLC患者预后关系的研究存在争议且分散。因此,迫切需要进行一项系统的荟萃分析,以探讨微小RNA对NSCLC患者的预后价值。 方法:检索电子数据库,包括PubMed、EMBASE和Web of Science,查找所有相关文章。本荟萃分析仅纳入研究微小RNA对NSCLC患者生存影响的文章。提取并汇总总生存期(OS)和无进展生存期(PFS)/疾病特异性生存期(DSS)的风险比(HR)及95%置信区间(CI)。 结果:最终28篇文章纳入总体荟萃分析。汇总结果显示,高表达的miR-21(HR = 2.82,95%CI:2.10 - 3.79)、miR-200c(HR = 2.05,95%CI:1.36 - 3.07)和miR-125b(HR = 1.72,95%CI:1.30 - 2.28)与NSCLC患者的生存呈负相关。相反,高表达的miR-148b(HR = 0.37,95%CI:0.19 - 0.70)、miR-365(HR = 0.40,95%CI:0.27 - 0.59)、miR-124(HR = 0.29,95%CI:0.16 - 0.53)、miR-32(HR = 0.46,95%CI:0.33 - 0.65)、miR-146a(HR = 0.35,95%CI:0.18 - 0.68)和miR-375(HR = 0.66,95%CI:0.45 - 0.96)与较好的预后显著相关。同时,miR-93(HR = 1.19,95%CI:0.38 - 3.69)和miR-126(HR = 0.38,95%CI:0.12 - 1.16)的表达与NSCLC预后无关。 结论:我们的荟萃分析提供了证据,表明miR-21、miR-200c、miR-125b、miR-148b、miR-365、miR-124、miR-32、miR-146a和miR-375可作为NSCLC的预后生物标志物。
Cochrane Database Syst Rev. 2018-2-6
Cochrane Database Syst Rev. 2016-5-25
Cochrane Database Syst Rev. 2022-1-7
Cochrane Database Syst Rev. 2022-9-26
Cochrane Database Syst Rev. 2018-1-16
Comput Struct Biotechnol J. 2024-12-24
World J Surg Oncol. 2021-9-1
Biomolecules. 2021-6-12
Int J Mol Sci. 2021-6-13