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Authors Ren Q, Li B, Liu M, Hu Z, Wang Y
Received 2 April 2018
Accepted for publication 5 July 2018
Published 18 October 2018 Volume 2018:11 Pages 7169—7178
DOI https://doi.org/10.2147/OTT.S169911
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Justinn Cochran
Peer reviewer comments 2
Editor who approved publication: Dr William Cho
Background and
objective: Many studies have reported that NEK2
is overexpressed in digestive system cancers (DSCs) and is also correlated with
patient survival. We performed a meta-analysis to comprehensively evaluate the
prognostic role of NEK2 expression in DSCs.
Materials and
methods: A comprehensive literature search
was performed using PubMed, EMBASE, and Web of Science. Synthesized hazard
ratios (HRs) and odds ratios (ORs) with 95% confidence intervals (CIs) were
used to evaluate the influence of NEK2 overexpression on the prognosis and
clinicopathological features of patients with DSCs.
Results: A total of 13 studies involving 1,917 patients was included.
Overall, patients with high NEK2 expression had poorer overall survival (HR
=1.45; 95% CI: 1.15–1.83; P =0.002) and
disease-free survival/recurrence-free survival (HR =2.28; 95% CI:
1.54–3.37; P <0.0001). Furthermore, subgroup
analysis also suggested that elevated NEK2 expression was associated with
poorer overall survival in patients with hepatocellular carcinoma (HR =1.45;
95% CI: 1.05–2.00; P =0.02) and
colorectal cancer (HR =2.03; 95% CI: 1.16–3.54; P =0.01). Additionally, NEK2
overexpression was also associated with pretreatment serum AFP level (OR =1.79;
95% CI: 1.23–2.61; P <0.01) and
portal vein thrombosis (OR =2.74; 95% CI: 1.22–6.17; P =0.01) in hepatocellular
carcinoma.
Conclusion: NEK2 might act as a useful prognostic predictor and a potential
therapeutic target in DSCs. However, multicenter homogeneous studies with
larger sample sizes are needed to further confirm our findings owing to some
limitations in our meta-analysis.
Keywords: NEK2, digestive system cancer, prognostic, meta-analysis
