Ma Peng-Ju, Guan Qing-Kai, Meng Lei, Qin Nan, Zhao Jia, Jin Bao-Zhe
Department of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang 453000, Henan Province, People's Republic of China.
Oncotarget. 2017 Jul 8;8(37):62454-62462. doi: 10.18632/oncotarget.19099. eCollection 2017 Sep 22.
LncRNA taurine upregulated gene 1 (TUG1) is reportedly dysregulated in various cancers. We performed this meta-analysis to clarify the usefulness of TUG1 as a prognostic marker in malignant tumors. The PubMed, Medline, OVID, Cochrane Library, and Web of Science databases were searched from inception to Jan 11, 2017. Hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated to explore the relationship between TUG1 expression and overall survival (OS). Odds ratios (ORs) were calculated to assess the association between TUG1 expression and pathological parameters. Thirteen original studies covering 1,274 cancer patients were included in this meta-analysis. The pooled HR suggested that high TUG1 expression correlated with poor OS (pooled HR=1.41, 95% CI: 1.01-1.98) in cancer types other than non-small cell lung cancer. TUG1 expression was also related to distant metastasis (OR=3.24, 95% CI: 1.18-8.93), large tumor size (OR=4.07, 95% CI: 1.08-15.28) and advanced tumor stage (OR=3.45, 95% CI: 2.19-5.44). Begg's funnel plot and Egger's test showed no evidence of obvious asymmetry for overall survival or tumor stage. Thus high TUG1 expression appears predictive of poor OS, distant metastasis, advanced tumor stage and large tumor size. This suggests TUG1 expression could serve as a biomarker for poor prognosis in cancers.
据报道,长链非编码RNA牛磺酸上调基因1(TUG1)在多种癌症中表达失调。我们进行了这项荟萃分析,以阐明TUG1作为恶性肿瘤预后标志物的效用。检索了PubMed、Medline、OVID、Cochrane图书馆和Web of Science数据库,检索时间从创建至2017年1月11日。计算风险比(HRs)和95%置信区间(CIs),以探讨TUG1表达与总生存期(OS)之间的关系。计算优势比(ORs),以评估TUG1表达与病理参数之间的关联。本荟萃分析纳入了13项涉及1274例癌症患者的原始研究。合并的HR表明,在非小细胞肺癌以外的癌症类型中,TUG1高表达与较差的OS相关(合并HR=1.41,95%CI:1.01-1.98)。TUG1表达还与远处转移(OR=3.24,95%CI:1.18-8.93)、肿瘤体积大(OR=4.07,95%CI:1.08-15.28)和肿瘤分期晚(OR=3.45,95%CI:2.19-5.44)有关。Begg漏斗图和Egger检验显示,总生存期或肿瘤分期均无明显不对称的证据。因此,TUG1高表达似乎预示着较差的OS、远处转移、肿瘤分期晚和肿瘤体积大。这表明TUG1表达可作为癌症预后不良的生物标志物。