Yan Xuefen, Zhang Nana, Wang Gang, Wang Jiaheng
The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, Zhejiang, China.
Front Genet. 2024 Mar 27;15:1362420. doi: 10.3389/fgene.2024.1362420. eCollection 2024.
Recent studies have revealed increasing evidence that the long non-coding RNA bladder cancer associated transcript 1 (LncRNA BLACAT1) plays an essential role in the emergence of different malignancies. This meta-analysis aimed to evaluate the prognostic significance of LncRNA BLACAT1 in various cancers.
Six electronic databases (PubMed, Embase, Medline, Web of Science, China National Knowledge Infrastructure (CNKI), and the Chinese WanFang database) were comprehensively searched for relevant studies. The analysis of overall survival (OS) and clinicopathological characteristics was conducted.
Nineteen studies with 1,559 patients were eventually eligible to be included in this meta-analysis. High expression level of LncRNA BLACAT1 was identified to be linked with shorter OS (HR: 2.02, 95% CI: 1.66-2.46, < 0.001) and PFS (HR: 2.424, 95% CI: 1.827-3.020, < 0.001) in cancer patients as opposed to low expression levels. Subgroup analysis showed that analysis model (multivariate or univariate), cut-off value (mean or median), sample size (more or fewer than 100), and cancer type had little effect on OS in multiple tumors. Moreover, high LncRNA BLACAT1 expression was associated with positive lymph node metastasis (HR: 2.29, 95% CI: 1.66-3.16, < 0.00001), advanced clinical stage (HR: 2.29, 95% CI: 1.65-3.19, < 0.00001) and worse differentiation status (HR: 0.58, 95% CI: 0.37-0.92, = 0.02), compared to low LncRNA BLACAT1 expression.
The findings highlight that high LncRNA BLACAT1 expression might be detrimental and induce a worse prognosis for cancer patients.
近期研究表明,越来越多的证据显示长链非编码RNA膀胱癌相关转录本1(LncRNA BLACAT1)在不同恶性肿瘤的发生中起重要作用。本荟萃分析旨在评估LncRNA BLACAT1在各种癌症中的预后意义。
全面检索了六个电子数据库(PubMed、Embase、Medline、Web of Science、中国国家知识基础设施数据库(CNKI)和中国万方数据库)中的相关研究。对总生存期(OS)和临床病理特征进行了分析。
最终有19项研究、1559例患者符合纳入本荟萃分析的标准。与低表达水平相比,LncRNA BLACAT1高表达水平与癌症患者较短的总生存期(HR:2.02,95%CI:1.66 - 2.46,P < 0.001)和无进展生存期(HR:2.424,95%CI:1.827 - 3.020,P < 0.001)相关。亚组分析显示,分析模型(多变量或单变量)、截断值(均值或中位数)、样本量(多于或少于100)和癌症类型对多种肿瘤的总生存期影响不大。此外,与LncRNA BLACAT1低表达相比,LncRNA BLACAT1高表达与阳性淋巴结转移(HR:2.29,95%CI:1.66 - 3.16,P < 0.00001)、晚期临床分期(HR:2.29,95%CI:1.65 - 3.19,P < 0.00001)和较差分化状态(HR:0.58,95%CI:0.37 - 0.92,P = 0.02)相关。
研究结果突出表明,LncRNA BLACAT1高表达可能有害,并导致癌症患者预后更差。