A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients

被引:30
|
作者
Zhang, Lan [1 ]
Shan, Xia [2 ]
Wang, Jun [3 ]
Zhu, Jun [4 ]
Huang, Zebo [1 ]
Zhang, Huo [1 ]
Zhou, Xin [1 ]
Cheng, Wenfang [5 ]
Shu, Yongqian [1 ]
Zhu, Wei [1 ]
Liu, Ping [1 ]
机构
[1] Nanjing Med Univ, Dept Oncol, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Respirat, Affiliated Jiangning Hosp, Nanjing 210000, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Thorac Surg, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
[4] Jiangsu Canc Hosp, Dept Radiat Oncol, Nanjing 210009, Jiangsu, Peoples R China
[5] Nanjing Med Univ, Dept Gastroenterol, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
serum microRNA; lung SCC; diagnostic biomarker; qRT-PCR; CIRCULATING MICRORNAS; NONINVASIVE BIOMARKERS; TUMOR PROGRESSION; SERUM MIRNAS; HIGH-RISK; CANCER; IDENTIFICATION; EXPRESSION; VALIDATION; MIR-93;
D O I
10.18632/oncotarget.19666
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Various studies have demonstrated the diagnostic value of microRNA (miRNA) for lung cancer, but miRNA signatures varied between different subtypes. Whether serum miRNAs could be used as biomarkers in lung squamous cell carcinoma (SCC) remains unknown. Using quantitative real-time polymerase chain reaction (qRT-PCR) based Exiqon panel, 38 differentially expressed miRNAs were identified from 3 male lung SCC pool samples and 1 normal control (NC) pool in the initial screening phase. After the training (24 SCC VS. 15 NCs), testing (44 SCC VS. 57 NCs) and external validation (34 SCC VS. 36 NCs VS. 10 pulmonary hamartoma) processes via qRTPCR, we identified a three-miRNA panel ((miR-106a-5p, miR-20a-5p and miR-935p) to be a potential diagnostic marker for male lung SCC patients. The areas under the receiver operating characteristic (ROC) curve of the three-miRNA panel for the training, testing and validation phases were 0.969, 0.881 and 0.954 respectively. In addition, this signature could also differentiate lung SCC from pulmonary hamartoma (AUC= 0.900). The 3 miRNAs were consistently up-regulated in lung SCC tissues (23 SCC VS. 23 NCs) and serum exosomes (17 SCC VS. 24 NCs). Moreover, expression of the 3 miRNAs was decreased in arterial serum (n = 3). In conclusion, we established a three-miRNA signature in the peripheral serum with considerable clinical value in the diagnosis of male lung SCC patients.
引用
收藏
页码:86897 / 86907
页数:11
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