Abstract

BackgroundLong intergenic non-coding RNA 00511 (LINC00511) is highly expressed in diverse cancers and has a correlation with poor clinical outcomes for cancer patients. In view of contradictory data among published data, we aim to evaluate the prognostic role of LINC00511 for cancer patients.MethodsIn the present study, a meta-analysis of related studies has been performed to investigate the prognostic significance of LINC00511 in cancer patients. Relevant studies published before December 22, 2019 were systematically searched online in PubMed, EMBASE, Web of Science, and the Cochrane Library databases. The relationship between LINC00511 expression and cancer patients’ survival, including overall survival (OS), disease-free survival (DFS)/relapse-free survival (RFS) and progression-free survival (PFS), was evaluated using pooled hazard ratios (HRs) with their corresponding 95% confidence intervals (CIs). The association between LINC00511 expression and clinicopathological features was assessed using odd ratios (ORs) and their corresponding 95% CIs.ResultsA total of 14 eligible studies with 1883 patients were enrolled in the present meta-analysis. The results demonstrated that elevated expression of LINC00511 was significantly associated with poor OS (HR = 2.62; 95% CI: 2.00–3.45; p < 0.001), PFS (HR = 1.80; 95% CI: 1.29–2.51; p = 0.001) and DFS/RFS (HR = 2.90; 95% CI: 1.04–8.12; p = 0.04). Additionally, High LINC00511 expression was associated with large tumor size (OR = 3.10; 95% CI: 1.97–4.86; p < 0.00001), lymph node metastasis (OR = 3.11; 95% CI: 2.30–4.21; p < 0.00001), advanced clinical stage (OR = 3.95; 95% CI: 2.68–5.81; p < 0.00001), distant metastasis (OR = 2.39; 95% CI: 1.16–4.93; p = 0.02), and disease recurrence (OR = 4.62; 95% CI: 2.47–8.65; p < 0.00001). Meanwhile, no correlation was found between LINC00511 expression and age, gender, and histological grade. These findings were consolidated by the results of bioinformatics analysis.ConclusionsBased on our findings, LINC00511 may serve as a novel prognostic biomarker for cancer patients.

Highlights

  • Long intergenic non-coding RNA 00511 (LINC00511) is highly expressed in diverse cancers and has a correlation with poor clinical outcomes for cancer patients

  • Inclusion and exclusion criteria The eligibility criteria were as follows: (1) the study subjects were patients with any type of cancer; (2) the studies investigated association between LINC00511 expression levels and clinical outcomes in cancer; (3) patients were separated into LINC00511 high expression level and LINC00511 low expression level groups; (4) the LINC00511 expression levels were measured by quantitative method (e.g., realtime reverse transcription polymerase chain reaction); and (5) sufficient information and data were provided to calculate a hazard ratios (HRs) or odd ratios (ORs) and their corresponding 95% confidence intervals (CIs)

  • The results showed that high LINC00511 expression was significantly associated with poor overall survival in lung neoplasms (HR = 3.86; 95% CI: 1.74– 8.54; p = 0.001; I2 = 80.5%; PH = 0.02), digestive system neoplasms (HR = 3.06; 95% CI: 2.76–3.40; p < 0.001; I2 = 0%; PH = 0.45), breast neoplasms (HR = 2.20; 95% CI: 1.50–3.23; p < 0.001; I2 = 0%; PH = 0.99) and urothelial neoplasms (HR = 3.15; 95% CI: 2.60–3.80; p < 0.001; I2 = 0%; PH = 0.80)

Read more

Summary

Introduction

Long intergenic non-coding RNA 00511 (LINC00511) is highly expressed in diverse cancers and has a correlation with poor clinical outcomes for cancer patients. Lu et al [16] detected significant correlation between LINC00511 overexpression and lymph node metastasis in breast cancer, whereas the study conducted by Zhang et al [26] provided a contradictory result. In view of these contradictory outcomes, we conducted a systematic review and meta-analysis to evaluate the prognostic role of LINC00511 for cancer patients. We validated our results by using The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) datasets

Objectives
Methods
Results
Discussion
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.