摘要
目的探讨长链非编码RNA(LncRNA)肝癌高表达转录本(HULC)的表达情况与肿瘤临床预后的关系。方法根据制定的纳入和排除标准,检索Pub Med、Embase和Cochrane Library数据库,筛选符合标准的研究,采用Review Manager 5.3软件进行统计学分析。结果共检出292篇相关文献,根据纳入和排除标准及文献质量评估方法共筛选出8篇文献,样本量为772例患者。荟萃分析的合并效应量显示,与HULC低表达组患者相比,HULC高表达组患者的总生存期较短(HR=2.10,95%CI:1.55~2.86,P﹤0.001)。根据肿瘤种类、患者国籍、样本类型进行分层亚组分析,在非肝癌组、胃肠道肿瘤组、非胃肠道肿瘤组、中国人群组、组织样本组中得到了相似的结果。OR值的合并效应量显示,过表达的HULC与多种临床病理特征有关。结论 LncRNA HULC在多种人类肿瘤中呈现过表达,这预示着较短的总生存期和较差的临床病理分期。
Objective To investigate the relationship between long-chain non-coding RNA (LncRNA) HULC (highly- up-regulated in liver cancer) and the clinical prognosis in cancer. Method PubMed, Embase and Cochrane Library data- bases were searched using established inclusion and exclusion criteria to retrieve the relevant studies. Statistical analysis was performed using Review Manager 5.3 software. Result A total of 292 relevant publications were retrieved, and 8 of which were included according to inclusion/exclusion criteria and quality evaluation standard of literature. The sample size was 772 patients. The combined effect in Meta-analysis indicated, the overall survival time in HULC overexpression group was longer than that in HULC lowexpression group (HR=2.10, 95%CI:1.55 to 2.86, P〈0.001). A subgroup analysis was performed using tumor type, patient nationality and sample type as stratification factors, and similar results were obtained in the non-hepatocellular carcinoma group, the gastrointestinal cancer group, the non-gastrointestinal cancer group, the Chinese patient group and the tissue sample group. The combined effect of OR value showed that overexpression of HULC was related to a variety of clinicopathological features. Conclusion LncRNA HULC is overexpressed in multiple human tumors, and indicates shorter overall survival time and worse clinical pathological stage.
作者
杨俊强
胡晓辰
刘怡文
高社干
YANG Junqiang;HU Xiaochen;LIU Yiwen;GAO Shegan(Department of Oncology, the First Affiliated Hospital of He'nan University of Science and Technology, Luoyang 471003, He'nan, China)
出处
《癌症进展》
2017年第8期929-932,949,共5页
Oncology Progress