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MicroRNA-25 expression level is an independent prognostic factor in epithelial ovarian cancer

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Abstract

Objectives

The present study aimed to investigate the expression level of MicroRNA-25 (miR-25) in epithelial ovarian cancer (EOC) tissue, and examine its relationship with clinicopathological factors and prognosis of patients with EOC.

Methods

Expression levels of miR-25 in 86 pairs of EOC tissue and adjacent normal tissue were measured by quantitative real-time reverse-transcription polymerase chain reaction (qRT-PCR). The comparison of the expression level of miR-25 between EOC tissue and adjacent normal tissue was performed using the two-sample Student’s t test. The correlation between the expression of miR-25 and clinicopathological characters was assessed with the two-sample Student’s t test. The overall survival was analyzed by log-rank test, and survival curves were plotted according to Kaplan–Meier.

Results

The expression level of miR-25 in EOC tissue was significantly higher than in adjacent normal tissue. The miR-25 expression level was significantly positively correlated with tumor stage, histology, and regional lymph node involvement (P < 0.05). Kaplan–Meier analysis showed that patients with higher levels of miR-25 had significantly poorer survival than those with lower expression of this miRNA in patients, with a 6-year overall survival of 15.96 and 45.89 %, respectively, (P = 0.001). In the multivariate Cox proportional hazards analysis, high miR-25 expression was independently associated with poor survival (P = 0.002; HR = 2.119; 95 % CI = 1.568–3.221).

Conclusion

The increased expression of miR-25 is closely related to poor prognosis of EOC, indicating that miR-25 may serve as a predictive biomarker for the prognosis of EOC.

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The authors declare no conflict of interest.

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Correspondence to X. Wang.

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Wang, X., Meng, X., Li, H. et al. MicroRNA-25 expression level is an independent prognostic factor in epithelial ovarian cancer. Clin Transl Oncol 16, 954–958 (2014). https://doi.org/10.1007/s12094-014-1178-6

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  • DOI: https://doi.org/10.1007/s12094-014-1178-6

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