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Prognostic and diagnostic potential of miR-146a in oesophageal squamous cell carcinoma

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 mi...

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Autores principales: Wang, Cong, Guan, Shanghui, Liu, Fang, Chen, Xuan, Han, Lihui, Wang, Ding, Nesa, Effat Un, Wang, Xintong, Bao, Cihang, Wang, Nana, Cheng, Yufeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742585/
https://www.ncbi.nlm.nih.gov/pubmed/26794279
http://dx.doi.org/10.1038/bjc.2015.463
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author Wang, Cong
Guan, Shanghui
Liu, Fang
Chen, Xuan
Han, Lihui
Wang, Ding
Nesa, Effat Un
Wang, Xintong
Bao, Cihang
Wang, Nana
Cheng, Yufeng
author_facet Wang, Cong
Guan, Shanghui
Liu, Fang
Chen, Xuan
Han, Lihui
Wang, Ding
Nesa, Effat Un
Wang, Xintong
Bao, Cihang
Wang, Nana
Cheng, Yufeng
author_sort Wang, Cong
collection PubMed
description 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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spelling pubmed-47425852017-02-02 Prognostic and diagnostic potential of miR-146a in oesophageal squamous cell carcinoma Wang, Cong Guan, Shanghui Liu, Fang Chen, Xuan Han, Lihui Wang, Ding Nesa, Effat Un Wang, Xintong Bao, Cihang Wang, Nana Cheng, Yufeng Br J Cancer Molecular Diagnostics 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. Nature Publishing Group 2016-02-02 2016-01-21 /pmc/articles/PMC4742585/ /pubmed/26794279 http://dx.doi.org/10.1038/bjc.2015.463 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Wang, Cong
Guan, Shanghui
Liu, Fang
Chen, Xuan
Han, Lihui
Wang, Ding
Nesa, Effat Un
Wang, Xintong
Bao, Cihang
Wang, Nana
Cheng, Yufeng
Prognostic and diagnostic potential of miR-146a in oesophageal squamous cell carcinoma
title Prognostic and diagnostic potential of miR-146a in oesophageal squamous cell carcinoma
title_full Prognostic and diagnostic potential of miR-146a in oesophageal squamous cell carcinoma
title_fullStr Prognostic and diagnostic potential of miR-146a in oesophageal squamous cell carcinoma
title_full_unstemmed Prognostic and diagnostic potential of miR-146a in oesophageal squamous cell carcinoma
title_short Prognostic and diagnostic potential of miR-146a in oesophageal squamous cell carcinoma
title_sort prognostic and diagnostic potential of mir-146a in oesophageal squamous cell carcinoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742585/
https://www.ncbi.nlm.nih.gov/pubmed/26794279
http://dx.doi.org/10.1038/bjc.2015.463
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