Combination of serum miRNAs with Cyfra21-1 for the diagnosis of non-small cell lung cancer

被引:54
|
作者
Zhou, Chengcheng
Chen, Zhaoli
Dong, Jingsi
Li, Jiagen
Shi, Xuejiao
Sun, Nan
Luo, Mei
Zhou, Fang
Tan, Fengwei
He, Jie [1 ]
机构
[1] Peking Union Med Coll, Dept Thorac Surg, Canc Inst & Hosp, Beijing 100021, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
Non-small cell lung cancer; Serum miRNA; Cyfra21-1; Diagnosis; PLASMA MICRORNA PANEL; CIRCULATING MICRORNAS; EXPRESSION; BIOMARKERS; PROGRESSION;
D O I
10.1016/j.canlet.2015.07.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this study, we screened 381 miRNAs by RT-qPCR in serum samples of 44 NSCLC patients and 22 healthy individuals to identify altered miRNAs, and validated the results in a training and test cohorts with 300 serum samples (178 NSCLC and 122 healthy individuals). Three miRNAs (miR-194, miR-652 and miR-660) were selected from 380 miRNAs by two normalization methods in the discovery cohort, and miR-652 and miR-660 were confirmed to be significantly upregulated in ADC and SCC patients compared with healthy controls both in the training and test cohorts (p < 0.01). The combination of miR-652 and miR-660 exhibited significantly higher AUC than miR-660, CEA and CA125 for ADC and SCC diagnosis in both the training and test cohorts (p < 0.05). Furthermore, miR-652 + miR-660 + Cyfra21-1 significantly improved the diagnostic ability to determine ADC patients from healthy controls. For SCC diagnosis, miR-652 + miR-660 + Cyfra21-1 exhibited comparable ability to Cyfra21-1. The results indicate that the combination of miR-652 + miR-660 and Cyfra21-1 has the potential to help in the diagnosis of NSCLC, especially for ADC. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:138 / 146
页数:9
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