Decreased expression of microRNA-148a predicts poor prognosis in ovarian cancer and associates with tumor growth and metastasis

• Published in: Biomedicine & pharmacotherapy 2016-10, Vol.83, p.58-63
• Main Authors: Gong, Li, Wang, Chongjuan, Gao, Yuan, Wang, Jie
• Format: Article
• Language: English
• Subjects: Cell Line, Tumor; Cell Movement - genetics; Cell Proliferation; Disease Progression; Female; Gene Expression Regulation, Neoplastic; Humans; Internal Medicine; Medical Education; Metastasis; MicroRNAs - blood; MicroRNAs - genetics; MicroRNAs - metabolism; Middle Aged; MiR-148a; Neoplasm Invasiveness; Neoplasm Metastasis; Ovarian cancer; Ovarian Neoplasms - blood; Ovarian Neoplasms - genetics; Ovarian Neoplasms - pathology; Prognosis; Proportional Hazards Models; Survival Analysis; Transfection
• ISSN: 0753-3322; 1950-6007
• DOI: 10.1016/j.biopha.2016.05.049

Abstract Objective MicroRNA-148a ( MiR-148a ) had been reported to take part in some cancer progresses, but its clinical significance in ovarian cancer had been rarely reported. The purpose of this study was to evaluate the prognostic value of miR-148a as well as its roles in ovarian cancer progression. Methods Relative expression of miR-148a in the plasma specimens of ovarian cancer patients was detected by qRT-PCR. Chi-square test was used to analyze the relationship between miR-148a expression and clinical characteristics. The overall survival was analyzed by Kaplan-Meier method and Cox regression analysis was used to evaluate the prognostic value of miR-148a . In addition, the ovarian cancer cell line SKOV-3 was separately transfected with pcDNA3-microRNA-148a over-expression vector and pcDNA3 empty vector to detect the functional roles of miR-148a in ovarian cancer progression. Results Decreased level of plasma miR-148a was observed in ovarian cancer patients compared with healthy controls. The expression level was associated with histopathologic grade, TNM stage and lymph node metastasis ( P < 0.05 for all). Besides, patients with high level of miR-148a had a longer survival time than those with low level (40.3 months vs 31.6 months, log rank test, P = 0.002). Cox regression analysis indicated that miR-148a might be a potential biomarker for ovarian cancer prognosis (HR = 1.699, 95%CI = 1.175-2.456, P = 0.005). Moreover, cell experiments confirmed that miR-148a could inhibit proliferation, migration and invasion of ovarian cancer cells. Conclusion MiR-148a may be a potential prognostic factor for ovarian cancer and it can suppress tumor progression.