临床肿瘤学杂志

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非小细胞肺癌血浆miR-223、miR-93和miR-218的表达及其临床意义

蔡静清1,王 宁2,张 敏2

  

  1. 1 067000 河北承德 承德市第三医院检验科2 067000 承德医学院附属医院检验科
  • 收稿日期:2014-08-30 修回日期:2014-10-17 出版日期:2014-12-31 发布日期:2014-12-31

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

摘要: 目的 探讨非小细胞肺癌(NSCLC)患者血浆miR-223、miR-93和miR-218水平,分析三者与NSCLC患者临床病理学特征的关系。方法 收集本院收治85例NSCLC患者未经治疗前的血浆标本(NSCLC组),采用实时定量RT-PCR(qRT-PCR)法检测血浆中miR-223、miR-93和miR-218水平,收集NSCLC患者的临床病理学参数,比较三者不同水平的临床病理参数并分析三者间的关系,采用受试者工作特征曲线(ROC)评价血浆miR223、miR93和miR218水平检测在NSCLC诊断中的临床价值。同时选取同期的90例健康体检者的血浆标本作对照(对照组)。结果 NSCLC组的血浆miR-223和miR-93水平高于对照组,miR-218水平低于对照组,差异均有统计学意义(P均<0.05);miR-223水平与TNM分期、肿瘤大小有关,miR-93水平与组织学类型、淋巴结转移有关,miR-218水平与肿瘤大小、分化程度有关,以上差异均有统计学意义(P<0.05);NSCLC患者血浆中miR-223水平与miR-93呈正相关(r=0.411),miR-223、miR-93分别与miR-218呈负相关(r=-0.361,r=-0.451),差异均有统计学意义(P<0.05);血浆miR-223、miR-93和miR-218诊断NSCLC的AUC、灵敏度和特异度分别为0.926、95.2%和87.1%,0.912、88.4%和92.5%,0.941、92.7%和84.4%,均高于CEA的0.774、75.1%和66.2%,且miR-223、miR-93和miR-218联合诊断的效能高于单独检测。结论 NSCLC患者血浆中miR-223和miR-93呈高表达,miR-218呈低表达,与临床病理学参数有关,且在NSCLC诊断中有一定的价值,可用于辅助NSCLC的诊断和病情评估。

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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