Journal
BRITISH JOURNAL OF CANCER
Volume 114, Issue 3, Pages 290-297Publisher
SPRINGERNATURE
DOI: 10.1038/bjc.2015.463
Keywords
ESCC; miR-146a; prognosis; diagnosis; tissue; serum; FFPE
Categories
Funding
- National Natural Science Foundation of China [81572958]
- Science and Technology Development Planning Project of Shandong Province [2014GSF118058]
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Background: Accumulating evidence indicates that dysregulated microRNA-146a (miR-146a) is involved in tumour genesis and cancer progression. We aimed to evaluate its expression level and the potential for the diagnosis and prognosis in oesophageal squamous cell cancer (ESCC). Methods: We examined miR-146a expression in 62 pairs of ESCC cancerous and matched paracancerous tissue, 115 formalin-fixed paraffin-embedded (FFPE) tissue samples and serum samples from 154 ESCC patients and 154 healthy volunteers using quantitative reverse transcription-PCR (qRT-PCR). Kaplan-Meier method, Cox regression and receiver-operating characteristic (ROC) curve analysis were applied to analyse its prognostic and diagnostic value. Results: MicroRNA-146a expression level was significantly decreased in ESCC tissue compared with paracancerous tissue (P < 0.001). Its regulation level was negatively associated with T factor and TNM stage. Kaplan-Meier curve revealed that its downregulation level predicted worse overall survival (OS) and progression-free survival (PFS). Both univariate and multivariate analyses identified miR-146a expression as independent prognostic factor for OS and PFS. Serum miR-146a was significantly reduced in ESCC patients than in healthy controls (P < 0.001). Area under the curve ROC value, sensitivity and specificity for this marker were 0.863 +/- 0.033, 85.7% and 68.6% in the Discovery Group, and 0.891 +/- 0.027, 82.1% and 83.3% in the Validation Group. Conclusions: MicroRNA-146a is significantly reduced in cancerous tissue and serum samples of ESCC patients. It is an ideal biomarker for the prognosis and diagnosis of ESCC.
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