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Prognostic value of lncRNA FEZF1 antisense RNA 1 over-expression in oncologic outcomes of patients with solid tumors.
Zhang, Yi; Yang, Qiu-Xi; Peng, Ting-Ting; Wang, Li-Juan; Xiao, Guo-Liang; Tang, Shu-Bin.
Affiliation
  • Zhang Y; Department of General Surgery, the First People's Hospital of Neijiang, Neijiang, Sichuan Province.
  • Yang QX; Department of Nursing, The First Affiliated Hospital of Hainan Medical University, Haikou, Hainan Province.
  • Peng TT; Department of Nursing, the First People's Hospital of Neijiang, Neijiang, Sichuan Province.
  • Wang LJ; Department of Nephrology, Shangrao People's Hospital, Shangrao, Jiangxi Province.
  • Xiao GL; Department of General Surgery, the First People's Hospital of Neijiang, Neijiang, Sichuan Province.
  • Tang SB; Department of Oncology, the First People's Hospital of Neijiang, Neijiang, Sichuan Province, P.R. China.
Medicine (Baltimore) ; 98(24): e15982, 2019 Jun.
Article in En | MEDLINE | ID: mdl-31192939
ABSTRACT

BACKGROUND:

FEZ family zinc finger 1 antisense RNA 1 (FEZF1-AS1), as a novel lncRNA, was reported to be up-regulated in various cancers and involved in tumor progression. This study systematically assessed the prognostic value of FEZF1-AS1 in solid tumors.

METHODS:

Web of Science, PubMed, EMBASE, Chinese National Knowledge Infrastructure, and Wanfang databases were searched for eligible studies that evaluated the prognostic role of FEZF1-AS1 expression in cancer patients. Pooled hazard ratios (HRs) and combined odds ratios (ORs) with their 95% confidence intervals (CIs) were calculated. The meta-analysis was conducted using Stata/SE 14.1.

RESULTS:

Fifteen original studies involving 1378 patients were enrolled. Pooled results showed that increased expression of FEZF1-AS1 significantly correlated with shorter overall survival (OS) in cancer patients (HR 2.04, 95% CI 1.60-2.47), and also shorter disease-free survival (DFS) (HR 2.08, 95% CI 1.27-2.89). Additionally, the combined ORs indicated that increased FEZF1-AS1 expression was significantly associated with lymph node metastasis (OR 3.35, 95% CI 1.98-5.67), distant metastasis (OR 3.10, 95% CI 1.86-5.15), poor tumor differentiation (OR 2.90, 95% CI 1.45-5.80), high depth of tumor invasion (OR 2.72, 95% CI 1.36-5.43), and advanced clinical stage (OR 2.76, 95% CI 1.75-4.35). Expression analysis using the Gene Expression Profiling Interactive Analysis database indicated that the expression of FEZF1-AS1 was higher in tumor tissues than that in the corresponding normal tissues. The results of survival analysis revealed that increased FEZF1-AS1 expression was correlated with poor OS and DFS in cancer patients.

CONCLUSIONS:

LncRNA FEZF1-AS1 may serve as a valuable prognostic biomarker for clinical outcomes in various solid tumors.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / RNA, Antisense / RNA, Long Noncoding / Neoplasms Type of study: Etiology_studies / Prognostic_studies / Systematic_reviews Limits: Humans Language: En Journal: Medicine (Baltimore) Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / RNA, Antisense / RNA, Long Noncoding / Neoplasms Type of study: Etiology_studies / Prognostic_studies / Systematic_reviews Limits: Humans Language: En Journal: Medicine (Baltimore) Year: 2019 Document type: Article