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Research Article

Clinicopathological and prognostic value of LINC01296 in cancers: a meta-analysis

, , , , , , & show all
Pages 3315-3321 | Received 30 Jun 2019, Accepted 18 Jul 2019, Published online: 06 Aug 2019
 

Abstract

Objective

The long intergenic non-coding RNA 01296 (LINC01296) has been reported to be overexpressed in multiple tumours. However, the role of LINC01296 in clinicopathologic and prognostic value in cancers remains completely unknown. The aim of the present meta-analysis was to comprehensively elucidate the correlation between LINC01296 with clinicopathological features and survival outcomes in tumours.

Methods

Electronic databases of PubMed, Web of Science, Chinese National Knowledge Infrastructure (CNKI), and Wanfang Database were used to search relevant studies. The role of LINC01296 in cancers was evaluated by pooled hazard ratios (HRs), odds ratios (ORs) and 95% confidence intervals (CIs).

Results

In total, nine studies compromising 720 participants were enrolled in this analysis. The pooled results showed increased LINC01296 expression could predict unfavourable overall survival (OS) (HR = 1.89, 95%CI = 1.47–2.43, p < .001). Additionally, elevated LINC01296 expression was correlated with clinical stage (OR = 2.95, 95%CI = 2.13–4.08, p < .001), lymph node metastasis (OR = 2.76, 95%CI = 2.00–3.81, p < .001), tumour size (OR = 2.80, 95%CI = 1.77–4.41, p < .001), and tumour differentiation (OR = 2.11, 95%CI = 1.36–3.27, p < .001) in patients with cancers.

Conclusion

The results of this meta-analysis indicated LINC01296 was a novel biomarker for prognosis and clinicopathological parameters in cancers.

Author contributions

W. F. designed the study, analyzed the data and wrote the manuscript; C. Z., and W. S. collected the data; Q. Z. and X. Y. participated in analyzing the data; J. W. and Q. W. took part in writing the manuscript; M. L. assisted in study design and revised the manuscript; All the authors have reviewed and approved the final proof.

Disclosure statement

All authors have declared there are no conflicts of interest.

Acknowledgements

The authors would thank Dr. Yang Song and Xiao Meng of Pfizer Medical for helpful suggestions.

Additional information

Funding

This work was supported by National Natural Science Foundation of China [81670051].