Down-regulation of long non-coding RNA MEG3 indicates an unfavorable prognosis in non-small cell lung cancer: Evidence from the GEO database

被引:26
作者
Zhang, Zichao [1 ,2 ]
Liu, Tiantian [1 ,3 ]
Wang, Kai [3 ,5 ]
Qu, Xiao [3 ]
Pang, Zhaofei [3 ]
Liu, Shaorui [3 ]
Liu, Qi [3 ]
Du, Jiajun [3 ,4 ]
机构
[1] Shandong Univ, Sch Med, 44 Cultural West Rd, Jinan 250012, Shandong, Peoples R China
[2] Linyi Hlth Sch Shandong Prov, Linyi 276002, Peoples R China
[3] Shandong Univ, Inst Oncol, Shandong Prov Hosp, 324 Jingwu Rd, Jinan 250021, Shandong, Peoples R China
[4] Shandong Univ, Dept Thorac Surg, Shandong Prov Hosp, 324 Jingwu Rd, Jinan 250021, Shandong, Peoples R China
[5] Shandong Univ, Dept Healthcare Resp, Shandong Prov Hosp, 324 Jingwu Rd, Jinan 250021, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
MEG3; NSCLC; Prognosis; GEO database; GENE-EXPRESSION; PROLIFERATION; STATISTICS; SIGNATURE; APOPTOSIS; HISTOLOGY; P53;
D O I
10.1016/j.gene.2017.08.001
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Long non-coding RNA (lncRNA) MEG3 (maternally expressed gene 3) is an imprinted gene that suppresses cells growth in various tumors. However, the association between MEG3 expression and prognosis in non-small cell lung cancer (NSCLC) has not been fully investigated. Seven datasets with 1144 patients were obtained from Gene Expression Omnibus (GEO) database (Affymetrix U133 Plus 2.0 platform). Association between MEG3 and other variables was tested using the chi-squared test. Kaplan-Meier survival analysis was carried out to explore the association between MEG3 expression and overall survival (OS)/progression free survival (PFS). Results of univariate and multivariate Cox regression analysis were represented in HR and 95%CI form. Summarized results and publication bias were showed by forest plots and funnel plots respectively. Differential expression of MEG3 was related to stage (GSE31210OS and GSE3121OPFS), histology (GSE29013OS and GSE29013PFS) and gender (GSE29013PFS). In summary, low MEG3 expression was associated with shorter long-term survival time in several datasets (GSE3141 (p = 0.039), GSE30219 (p = 0.008) for OS and GSE30219 (p = 0.048) for PFS). We found that MEG3 was an independent prognostic factor in GSE30219 for PFS (HR 0.666, 95%CI 0.458-0.969, p = 0.033). The summarized results suggested that low MEG3 expression was a poor prognostic factor in NSCLC (HR = 0.77, 95%CI 0.63-0.95). Specifically, the association between low MEG3 expression and poor prognosis was markedly significant in younger patients (<= 60 years old) (HR0.602, 95%CI 0.417-0.867, p = 0.007). These findings indicate that MEG3 could be a novel prognostic factor for NSCLC patients.
引用
收藏
页码:49 / 58
页数:10
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