4.6 Article

microRNA-944 overexpression is a biomarker for poor prognosis of advanced cervical cancer

Journal

BMC CANCER
Volume 19, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12885-019-5620-6

Keywords

microRNAs; Survival; Prognosis; Uterine cervical neoplasm

Categories

Funding

  1. Basic Science Research Program of the National Research Foundation of Korea (NRF) - Ministry of Science, ICT, and Future Planning [2015R1A2A2A04004455]
  2. National Research Foundation of Korea [2015R1A2A2A04004455] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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BackgroundOne-third of cervical cancer patients are still diagnosed at advanced stages. The five-year survival rate is decreased in about 50% of advanced stage cervical cancer patients worldwide, and the clinical outcomes are remarkably varied and difficult to predict. One of the miRNAs known to be associated with cancer tumorigenesis is miR-944. However, the prognostic value of miR-944 in cervical cancer has not been fully investigated. The aim of this study was to analyze clinical significance and prognostic value of miR-944 in cervical cancer.MethodsThe expression levels of miR-944 were detected using quantitative reverse transcription polymerase chain reaction in five types of cervical cancer cell lines and 116 formalin-fixed paraffin-embedded (FFPE) cervical tissues. The association between the expression levels of miR-944 and prognostic value was analyzed using the Kaplan-Meier analysis and Cox proportional hazards model.ResultsThe expression levels of miR-944 in cervical cancer tissues were significantly higher compared with those in normal tissues (P<0.0001). Moreover, the expression levels of miR-944 in cervical cancer cell lines and FFPE tissues with human papillomavirus (HPV) infection were significantly higher compared to those without HPV infection (P<0.01 and P=0.02). High miR-944 expression was also markedly associated with bulky tumor size (P=0.026), advanced International Federation of Gynecology and Obstetrics (FIGO) stage (P=0.042), and lymph node metastasis (P=0.030). In particular, high miR-944 expression group showed shorter overall survival than the low miR-944 expression group in the advanced FIGO stage (84.4% vs. 44.4%, HR=4.0, and P=0.01).ConclusionsThese results suggest that miR-944 may be used as a novel biomarker for improving prognosis and as a potential therapeutic target.

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