Oncology Letters · 2017 · 34 citations · 47 references
MedicineOncologyPathologyGynecologic OncologyMetastasisMolecular OncologyCancer BiomarkersCancer Survival AnalysisMalignant NeoplasmsNoncoding Rna In CancerOvarian CancerTumor MarkersCancer Antigen 125Microrna In CancerMicrorna Prognostic MarkersOvarian Cancer Prognostic BiomarkersPrognostic Marker AssessmentPrognostic Marker EvaluationRisk Of Malignancy IndexSerous Ovarian Tumors
The aim of the present retrospective study was to compare microRNA (miR)-146a expression levels in primary tumors and omental metastases of 48 patients, who had undergone surgery for advanced ovarian serous cancer. Possible correlations between miR-146a expression level and clinicopathological features were investigated, including chemosensitivity and survival. miR-146a was evaluated in formalin-fixed, paraffin-embedded samples. miR-146a expression level in primary tumors was demonstrated to be increased in comparison with normal ovary tissues (P=0.02) and metastases (P=0.01). A negative correlation was demonstrated between miR-146a expression in primary tumors and serum levels of cancer antigen 125 (R=-0.37; P=0.03) and Risk of Malignancy Algorithm index (R=-0.79; P=0.0007). Overall survival positively correlated with miR-146a expression in primary tumor tissue samples (R=0.38; P=0.01). Probability of survival was decreased in patients with low miR-146a expression levels in primary tumor tissues (hazard ratio=0.21; P=0.003). Lower levels of miR-146a in primary tumor tissue samples were correlated with a shorter progression-free survival (P=0.04) and platinum-resistance of metastases (P=0.006). In conclusion, miR-146a may be a prognostic marker for serous ovarian cancer.
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