Chinese Clinical Oncology

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Expression and clinical value analysis of plasma miR-223, miR-93 and miR-218 in non-small lung cancer

CAI Jingqing, WANG Ning, ZHANG Min.
  

  1. Department of Laboratory Medicine, the Third Hospital of Chengde, Chengde 067000, China
  • Received:2014-08-30 Revised:2014-10-17 Online:2014-12-31 Published:2014-12-31

Abstract: Objective To explore the levels of plasma miR-223, miR-93 and miR-218 in non-small lung cancer(NSCLC) and analysis the relationship between the 3 indicators and clinicopathological parameters of NSCLC.
Methods Plasma samples from 85 NSCLC patients before treatment were collected as NSCLC group. The real-time quantitative RT-PCR(qRT-PCR) was used to detect the levels of miR-223, miR-93 and miR-218 and the clinicopathological parameters of NSCLC patients were collected. The clinicopathological parameters of patients with different levels of miR-223, miR-93 and miR-218 were compared. The receiver operating characteristic curve(ROC) was employed to analysis the clinical value of plasma miR-223, miR-93 and miR-218 in the diagnosis of NSCLC. Meanwhile, the plasma samples from 90 healthy volunteers at the same time were selected as control(control group). Results There were higher levels of miR-223 and miR-93 but lower miR-218 in NSCLC group compaired with control group with significant difference(P<0.05). The level of miR-223 was related with TNM stage and tumor size, and miR-93 was related with histological type and lymph node metastasis, and miR-218 was related with tumor size and degree of differentiation, showing with significant difference(P all<0.05). The plasma level of miR-223 was positively correlated with miR-93(r=0.411), but miR-223 and miR-93 were negatively correlated with miR-218(r=-0.361 and r=-0.451)with statistically significance(P<0.05). The AUC, sensitivity and specificity of plasma miR-223, miR-93 and miR218 in the diagnosis of NSCLC were 0.926, 95.2% and 87.1%, 0.912, 88.4% and 92.5%, and 0.941, 92.7% and 84.4%, higher than 0.774, 75.1% and 66.2% of carcinoembryonic antigen(CEA). The combined efficiency of miR-223, miR-93 and miR-218 in NSCLC was superior to that alone. Conclusion There are higher expression of miR-223 and miR-93 but lower expression of miR-218 in NSCLC. The plasma levels of the above indicators are related with clinical pathology parameters, showing a certain value in the diagnosis of NSCLC as assisted indicators in the diagnosis of NSCLC.

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