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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.
Afiliação
  • Wang C; Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, China.
  • Guan S; Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, China.
  • Liu F; Department of Imaging, Shandong Medical College, Jinan, Shandong 250002, China.
  • Chen X; Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, China.
  • Han L; Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, China.
  • Wang D; Department of Laboratory Medicine, Qilu Hospital of Shandong University, Jinan, Shandong 250012, China.
  • Nesa EU; Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, China.
  • Wang X; Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Jinan, Shandong 250117, China.
  • Bao C; Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
  • Wang N; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
  • Cheng Y; Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, China.
Br J Cancer ; 114(3): 290-7, 2016 Feb 02.
Article em En | MEDLINE | ID: mdl-26794279
ABSTRACT

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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Carcinoma de Células Escamosas / Biomarcadores Tumorais / MicroRNAs Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Carcinoma de Células Escamosas / Biomarcadores Tumorais / MicroRNAs Idioma: En Ano de publicação: 2016 Tipo de documento: Article