Li Yang, Yang Ze, Wan Xiaoya, Zhou Jianguo, Zhang Yu, Ma Hu, Bai Yuju
Department of Oncology, Affiliated Hospital of Zunyi Medical University, Zunyi Medical University, Zunyi - PR China.
Int J Biol Markers. 2016 May 28;31(2):e173-82. doi: 10.5301/jbm.5000185.
Many studies have investigated the prognostic value of metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) in human cancers. However, these studies were often limited by small sample sizes. Therefore, we performed this updated meta-analysis to summarize the potential value of MALAT1 as a biomarker for early treatment and to predict survival in various human malignant neoplasms, through the inclusion of the latest literature and improved methodology.
Twelve eligible articles were systematically obtained from PubMed, Medline, Embase, Web of Science, China National Knowledge Infrastructure and the Cochrane Library, from inception up to June 30, 2015. Survival was assessed using pooled hazard ratios (HRs) and 95% confidence intervals (95% CIs).
By combining the results of 12 studies, we found elevated MALAT1 expression was associated with poor survival in most cancers, with a pooled HR of 1.90 (95% CI, 1.56-2.30) for overall survival (OS) and 3.06 (95% CI, 2.06-4.56) for recurrence-free survival/disease-free survival. Subgroup analyses according to ethnicity, tumor type, assay method, sample size, HR-calculation method and analysis type did not affect the predictive role of MALAT1 for OS in various cancer types. Further, by combining results from studies that used multivariate analyses, we found elevated MALAT1 was an independent prognostic factor for OS (HR = 1.98; 95% CI, 1.58-2.48).
MALAT1 could serve as a potential prognostic biomarker in various cancers and may be a potential therapeutic target for the treatment and early detection of recurrence.
许多研究探讨了转移相关的肺腺癌转录本1(MALAT1)在人类癌症中的预后价值。然而,这些研究往往受限于样本量较小。因此,我们进行了这项更新的荟萃分析,通过纳入最新文献并改进方法,总结MALAT1作为早期治疗生物标志物以及预测各种人类恶性肿瘤生存情况的潜在价值。
从PubMed、Medline、Embase、Web of Science、中国知网和Cochrane图书馆系统检索了12篇符合条件的文章,检索时间从建库至2015年6月30日。使用合并风险比(HR)和95%置信区间(95%CI)评估生存情况。
综合12项研究的结果,我们发现大多数癌症中MALAT1表达升高与较差的生存相关,总生存(OS)的合并HR为1.90(95%CI,1.56 - 2.30),无复发生存/无病生存的合并HR为3.06(95%CI,2.06 - 4.56)。根据种族、肿瘤类型、检测方法、样本量、HR计算方法和分析类型进行的亚组分析,均不影响MALAT1对各种癌症类型OS的预测作用。此外,通过合并使用多因素分析的研究结果,我们发现MALAT1表达升高是OS的独立预后因素(HR = 1.98;95%CI,1.58 - 2.48)。
MALAT1可作为多种癌症潜在的预后生物标志物,可能是治疗及早期复发检测的潜在治疗靶点。